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A novel mode of chromosomal evolution peculiar to filamentous Ascomycete fungi

Identifieur interne : 002557 ( Pmc/Corpus ); précédent : 002556; suivant : 002558

A novel mode of chromosomal evolution peculiar to filamentous Ascomycete fungi

Auteurs : James K. Hane ; Thierry Rouxel ; Barbara J. Howlett ; Gert Hj Kema ; Stephen B. Goodwin ; Richard P. Oliver

Source :

RBID : PMC:3219968

Abstract

Background

Gene loss, inversions, translocations, and other chromosomal rearrangements vary among species, resulting in different rates of structural genome evolution. Major chromosomal rearrangements are rare in most eukaryotes, giving large regions with the same genes in the same order and orientation across species. These regions of macrosynteny have been very useful for locating homologous genes in different species and to guide the assembly of genome sequences. Previous analyses in the fungi have indicated that macrosynteny is rare; instead, comparisons across species show no synteny or only microsyntenic regions encompassing usually five or fewer genes. To test the hypothesis that chromosomal evolution is different in the fungi compared to other eukaryotes, synteny was compared between species of the major fungal taxa.

Results

These analyses identified a novel form of evolution in which genes are conserved within homologous chromosomes, but with randomized orders and orientations. This mode of evolution is designated mesosynteny, to differentiate it from micro- and macrosynteny seen in other organisms. Mesosynteny is an alternative evolutionary pathway very different from macrosyntenic conservation. Surprisingly, mesosynteny was not found in all fungal groups. Instead, mesosynteny appears to be restricted to filamentous Ascomycetes and was most striking between species in the Dothideomycetes.

Conclusions

The existence of mesosynteny between relatively distantly related Ascomycetes could be explained by a high frequency of chromosomal inversions, but translocations must be extremely rare. The mechanism for this phenomenon is not known, but presumably involves generation of frequent inversions during meiosis.


Url:
DOI: 10.1186/gb-2011-12-5-r45
PubMed: 21605470
PubMed Central: 3219968

Links to Exploration step

PMC:3219968

Le document en format XML

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<p>Gene loss, inversions, translocations, and other chromosomal rearrangements vary among species, resulting in different rates of structural genome evolution. Major chromosomal rearrangements are rare in most eukaryotes, giving large regions with the same genes in the same order and orientation across species. These regions of macrosynteny have been very useful for locating homologous genes in different species and to guide the assembly of genome sequences. Previous analyses in the fungi have indicated that macrosynteny is rare; instead, comparisons across species show no synteny or only microsyntenic regions encompassing usually five or fewer genes. To test the hypothesis that chromosomal evolution is different in the fungi compared to other eukaryotes, synteny was compared between species of the major fungal taxa.</p>
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<sec>
<title>Results</title>
<p>These analyses identified a novel form of evolution in which genes are conserved within homologous chromosomes, but with randomized orders and orientations. This mode of evolution is designated mesosynteny, to differentiate it from micro- and macrosynteny seen in other organisms. Mesosynteny is an alternative evolutionary pathway very different from macrosyntenic conservation. Surprisingly, mesosynteny was not found in all fungal groups. Instead, mesosynteny appears to be restricted to filamentous Ascomycetes and was most striking between species in the Dothideomycetes.</p>
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<title>Conclusions</title>
<p>The existence of mesosynteny between relatively distantly related Ascomycetes could be explained by a high frequency of chromosomal inversions, but translocations must be extremely rare. The mechanism for this phenomenon is not known, but presumably involves generation of frequent inversions during meiosis.</p>
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</TEI>
<pmc article-type="research-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Genome Biol</journal-id>
<journal-title-group>
<journal-title>Genome Biology</journal-title>
</journal-title-group>
<issn pub-type="ppub">1465-6906</issn>
<issn pub-type="epub">1465-6914</issn>
<publisher>
<publisher-name>BioMed Central</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">21605470</article-id>
<article-id pub-id-type="pmc">3219968</article-id>
<article-id pub-id-type="publisher-id">gb-2011-12-5-r45</article-id>
<article-id pub-id-type="doi">10.1186/gb-2011-12-5-r45</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Research</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>A novel mode of chromosomal evolution peculiar to filamentous Ascomycete fungi</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" id="A1">
<name>
<surname>Hane</surname>
<given-names>James K</given-names>
</name>
<xref ref-type="aff" rid="I1">1</xref>
<xref ref-type="aff" rid="I2">2</xref>
<email>James.hane@csiro.au</email>
</contrib>
<contrib contrib-type="author" id="A2">
<name>
<surname>Rouxel</surname>
<given-names>Thierry</given-names>
</name>
<xref ref-type="aff" rid="I3">3</xref>
<email>rouxel@versailles.inra.fr</email>
</contrib>
<contrib contrib-type="author" id="A3">
<name>
<surname>Howlett</surname>
<given-names>Barbara J</given-names>
</name>
<xref ref-type="aff" rid="I4">4</xref>
<email>bhowlett@unimelb.edu.au</email>
</contrib>
<contrib contrib-type="author" id="A4">
<name>
<surname>Kema</surname>
<given-names>Gert HJ</given-names>
</name>
<xref ref-type="aff" rid="I5">5</xref>
<email>gert.kema@wur.nl</email>
</contrib>
<contrib contrib-type="author" id="A5">
<name>
<surname>Goodwin</surname>
<given-names>Stephen B</given-names>
</name>
<xref ref-type="aff" rid="I6">6</xref>
<email>sgoodwin@purdue.edu</email>
</contrib>
<contrib contrib-type="author" corresp="yes" id="A6">
<name>
<surname>Oliver</surname>
<given-names>Richard P</given-names>
</name>
<xref ref-type="aff" rid="I7">7</xref>
<email>richard.oliver@curtin.edu.au</email>
</contrib>
</contrib-group>
<aff id="I1">
<label>1</label>
CSIRO Plant Industry, Centre for Environment and Life Sciences, Private Bag 5, Perth, 6193, Australia</aff>
<aff id="I2">
<label>2</label>
Faculty of Health Sciences, Murdoch University, Perth, 6150, Australia</aff>
<aff id="I3">
<label>3</label>
INRA-Bioger, Avenue Lucien Brétignières, BP 01, Thiverval-Grignon, 78850, France</aff>
<aff id="I4">
<label>4</label>
School of Botany, The University of Melbourne, Melbourne, 3010, Australia</aff>
<aff id="I5">
<label>5</label>
Wageningen UR, Plant Research International, Department of Biointeractions and Plant Health, PO Box 69, Wageningen, 6700 AB, The Netherlands</aff>
<aff id="I6">
<label>6</label>
USDA-ARS, Crop Production and Pest Control Research Unit, Purdue University, 915 West State Street, West Lafayette, IN 47907-2054, USA</aff>
<aff id="I7">
<label>7</label>
Australian Centre for Necrotrophic Fungal Pathogens, Curtin University, Perth, 6845, Australia</aff>
<pub-date pub-type="ppub">
<year>2011</year>
</pub-date>
<pub-date pub-type="epub">
<day>24</day>
<month>5</month>
<year>2011</year>
</pub-date>
<volume>12</volume>
<issue>5</issue>
<fpage>R45</fpage>
<lpage>R45</lpage>
<history>
<date date-type="received">
<day>20</day>
<month>2</month>
<year>2011</year>
</date>
<date date-type="rev-recd">
<day>27</day>
<month>4</month>
<year>2011</year>
</date>
<date date-type="accepted">
<day>24</day>
<month>5</month>
<year>2011</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright ©2011 Hane et al.; licensee BioMed Central Ltd.</copyright-statement>
<copyright-year>2011</copyright-year>
<copyright-holder> Hane et al.; licensee BioMed Central Ltd.</copyright-holder>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/2.0">
<license-p>This is an open access article distributed under the terms of the Creative Commons Attribution License (
<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/2.0">http://creativecommons.org/licenses/by/2.0</ext-link>
), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<self-uri xlink:href="http://genomebiology.com/2011/12/5/R45"></self-uri>
<abstract>
<sec>
<title>Background</title>
<p>Gene loss, inversions, translocations, and other chromosomal rearrangements vary among species, resulting in different rates of structural genome evolution. Major chromosomal rearrangements are rare in most eukaryotes, giving large regions with the same genes in the same order and orientation across species. These regions of macrosynteny have been very useful for locating homologous genes in different species and to guide the assembly of genome sequences. Previous analyses in the fungi have indicated that macrosynteny is rare; instead, comparisons across species show no synteny or only microsyntenic regions encompassing usually five or fewer genes. To test the hypothesis that chromosomal evolution is different in the fungi compared to other eukaryotes, synteny was compared between species of the major fungal taxa.</p>
</sec>
<sec>
<title>Results</title>
<p>These analyses identified a novel form of evolution in which genes are conserved within homologous chromosomes, but with randomized orders and orientations. This mode of evolution is designated mesosynteny, to differentiate it from micro- and macrosynteny seen in other organisms. Mesosynteny is an alternative evolutionary pathway very different from macrosyntenic conservation. Surprisingly, mesosynteny was not found in all fungal groups. Instead, mesosynteny appears to be restricted to filamentous Ascomycetes and was most striking between species in the Dothideomycetes.</p>
</sec>
<sec>
<title>Conclusions</title>
<p>The existence of mesosynteny between relatively distantly related Ascomycetes could be explained by a high frequency of chromosomal inversions, but translocations must be extremely rare. The mechanism for this phenomenon is not known, but presumably involves generation of frequent inversions during meiosis.</p>
</sec>
</abstract>
</article-meta>
</front>
<body>
<sec>
<title>Background</title>
<p>The evolutionary history of organisms, as revealed by comparisons of genome sequences, is of the greatest biological significance and interest. The current explosion in the number of genome assemblies of species within the same class, order and genus is allowing the whole-genome interrelationships between organisms to be examined in ever greater detail. There is a long history of comparisons of individual orthologous gene sequences and these have revolutionized our understanding of phylogenetic relationships [
<xref ref-type="bibr" rid="B1">1</xref>
]. A more complete understanding of both the mechanism and results of evolution can be obtained by comparing entire genomes [
<xref ref-type="bibr" rid="B2">2</xref>
]. These comparisons have refined the concept of synteny. This term is used loosely by many authors. Originally it was used in cytogenetics to describe two or more loci that are located on the same chromosome. As DNA sequencing and comparative genomics became commonplace, the term synteny acquired the additional property of co-linearity; i.e. the conservation of gene order and orientation. In this study we refer to synteny in the original cytogenetic sense and describe co-linearity as a sub-category of synteny. If orthologs of multiple genes that are co-located in the genome of one organism are co-located in another species, the chromosomes on which the genes reside are said to be syntenic. Synteny can also be quantitative; chromosomes that contain all of the same genes are 100% syntenic.</p>
<p>The process of speciation occurs when two independent populations diverge into reproductively isolated species. Initially the daughter species would have had chromosomes that shared both gene content (synteny) and order (co-linearity). Over evolutionary time, the degree of synteny and co-linearity would be degraded through various processes, including chromosomal duplications, gene losses/gains and chromosomal rearrangements (Additional file
<xref ref-type="supplementary-material" rid="S1">1</xref>
), until orthologous genes in one species occur randomly in the genome of the other.</p>
<p>The related concepts of synteny and co-linearity have been refined mostly in plants, animals and bacteria. Synteny has been differentiated qualitatively based on the length and completeness of co-linear regions. Macrosynteny describes co-linearity observable at a whole-chromosome scale, involving hundreds or thousands of genes of which a backbone are co-linear. Microsynteny describes co-linearity spanning a small number (for example, two to ten) of successive genes. Comparisons of vertebrate and flowering plant species within taxonomic families often have shown extensive macrosynteny [
<xref ref-type="bibr" rid="B3">3</xref>
-
<xref ref-type="bibr" rid="B8">8</xref>
]. Macrosynteny has been exploited to assist genetic mapping and gene cloning; examples include the use of the
<italic>Arabidopsis </italic>
genome to find genes in canola [
<xref ref-type="bibr" rid="B9">9</xref>
], and rice/
<italic>Brachypodium </italic>
synteny to locate genes in wheat and barley [
<xref ref-type="bibr" rid="B10">10</xref>
].</p>
<p>Filamentous fungi form an ancient, large and diverse group of organisms. Until the last decade, the phylogenetics of fungi was problematic but the application of techniques based on gene sequence variation has created a stable taxonomy. The ascomycete filamentous fungi are mostly within the sub-phylum Pezizomycotina (Figure
<xref ref-type="fig" rid="F1">1</xref>
) [
<xref ref-type="bibr" rid="B11">11</xref>
]. This sub-phylum contains four major classes: Dothideomycetes, Eurotiomycetes, Sordariomycetes and Leotiomycetes. The Dothideomycetes contains more than 20,000 species amongst which are many of the most important plant pathogens worldwide, including those in the genera
<italic>Phaeosphaeria</italic>
,
<italic>Leptosphaeria </italic>
and
<italic>Mycosphaerella</italic>
.</p>
<fig id="F1" position="float">
<label>Figure 1</label>
<caption>
<p>
<bold>Cladogram of species used in whole-genome comparisons in this study</bold>
. Detailed information on each species is provided in Additional file
<xref ref-type="supplementary-material" rid="S3">3</xref>
.</p>
</caption>
<graphic xlink:href="gb-2011-12-5-r45-1"></graphic>
</fig>
<p>Evolutionary diversity within the filamentous ascomycete fungi is much higher than in flowering plants or vertebrate animals [
<xref ref-type="bibr" rid="B12">12</xref>
]. A number of reasons have been proposed to account for this. Filamentous fungi reflect approximately 400 million years of evolutionary history, comparable to that of the vertebrates but approximately four times longer than that of the flowering plants [
<xref ref-type="bibr" rid="B13">13</xref>
] (Figure
<xref ref-type="fig" rid="F1">1</xref>
; Table
<xref ref-type="table" rid="T1">1</xref>
). The generation times of fungi are typically measured in hours or days, whereas plants and animals have generation times of many weeks, years or even decades. Meiosis is a powerful force stabilising chromosomal structure and may occur less commonly in some fungi compared to plants and animals; whilst nearly all filamentous fungi undergo germline asexual reproduction, only a subset have known sexual phases. Furthermore, many filamentous fungi can acquire genetic material by lateral gene transfer, which can increase their rate of evolution [
<xref ref-type="bibr" rid="B14">14</xref>
-
<xref ref-type="bibr" rid="B16">16</xref>
]. All of these factors would tend to reduce or eliminate the extent of synteny between species. It was not surprising, therefore, when initial comparisons between fungal genome sequences failed to find extensive evidence of interspecific macro- or microsynteny [
<xref ref-type="bibr" rid="B17">17</xref>
-
<xref ref-type="bibr" rid="B22">22</xref>
] and, with the exception of the aspergilli, even between species from the same genus [
<xref ref-type="bibr" rid="B23">23</xref>
-
<xref ref-type="bibr" rid="B25">25</xref>
].</p>
<table-wrap id="T1" position="float">
<label>Table 1</label>
<caption>
<p>Summary of whole-genome synteny relationships across selected fungal orders</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th></th>
<th align="left">Sub-phylum</th>
<th align="center" colspan="8">Pezizomycotina</th>
<th align="center">Saccharomycotina</th>
<th align="center">Taphrinomycotina</th>
</tr>
<tr>
<th></th>
<th colspan="9">
<hr></hr>
</th>
<th colspan="2">
<hr></hr>
</th>
</tr>
<tr>
<th></th>
<th align="left">Class</th>
<th align="center" colspan="2">Dothideomycetes</th>
<th align="center" colspan="2">Eurotiomycetes</th>
<th align="center" colspan="3">Sordariomycetes</th>
<th align="center">Leotiomycetes</th>
<th align="center">Saccharomycetes</th>
<th align="center">Schizosaccharomycetes</th>
</tr>
<tr>
<th></th>
<th colspan="3">
<hr></hr>
</th>
<th colspan="2">
<hr></hr>
</th>
<th colspan="3">
<hr></hr>
</th>
<th colspan="1">
<hr></hr>
</th>
<th colspan="2">
<hr></hr>
</th>
</tr>
<tr>
<th align="left">Class</th>
<th align="left">Order</th>
<th align="center">Capnodiales</th>
<th align="center">Pleosporales</th>
<th align="center">Eurotiales</th>
<th align="center">Onygenales</th>
<th align="center">Hypocreales</th>
<th align="center">Magnaporthales</th>
<th align="center">Sordariales</th>
<th align="center">Helotiales</th>
<th align="center">Saccharomycetales</th>
<th align="center">Schizosaccharomycetales</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left">Dothideomycetes</td>
<td align="left">Capnodiales</td>
<td align="center">Meso/150</td>
<td align="center">Meso</td>
<td align="center">Demeso</td>
<td align="center">Demeso</td>
<td align="center">Demeso</td>
<td align="center">None</td>
<td align="center">Demeso</td>
<td align="center">Demeso</td>
<td align="center">None</td>
<td align="center">None</td>
</tr>
<tr>
<td></td>
<td align="left">Pleosporales</td>
<td align="center">300</td>
<td align="center">Meso/120</td>
<td align="center">Demeso</td>
<td align="center">Demeso</td>
<td align="center">Demeso</td>
<td align="center">None</td>
<td align="center">Demeso</td>
<td align="center">Demeso</td>
<td align="center">None</td>
<td align="center">None</td>
</tr>
<tr>
<td align="left">Eurotiomycetes</td>
<td align="left">Eurotiales</td>
<td align="center">370</td>
<td align="center">370</td>
<td align="center">Demacro/< 160</td>
<td align="center">Demacro</td>
<td align="center">None</td>
<td align="center">None</td>
<td align="center">None</td>
<td align="center">Demeso</td>
<td align="center">None</td>
<td align="center">None</td>
</tr>
<tr>
<td></td>
<td align="left">Onygenales</td>
<td align="center">370</td>
<td align="center">370</td>
<td align="center">150</td>
<td align="center">Demacro/< 160</td>
<td align="center">None</td>
<td align="center">None</td>
<td align="center">None</td>
<td align="center">Demeso</td>
<td align="center">None</td>
<td align="center">None</td>
</tr>
<tr>
<td align="left">Sordariomycetes</td>
<td align="left">Hypocreales</td>
<td align="center">370</td>
<td align="center">370</td>
<td align="center">370</td>
<td align="center">370</td>
<td align="center">Macro/170</td>
<td align="center">Demeso</td>
<td align="center">Demeso</td>
<td align="center">Demeso</td>
<td align="center">None</td>
<td align="center">None</td>
</tr>
<tr>
<td></td>
<td align="left">Magnaporthales</td>
<td align="center">370</td>
<td align="center">370</td>
<td align="center">370</td>
<td align="center">370</td>
<td align="center">240</td>
<td align="center">NA</td>
<td align="center">Demeso</td>
<td align="center">Demeso</td>
<td align="center">None</td>
<td align="center">None</td>
</tr>
<tr>
<td></td>
<td align="left">Sordariales</td>
<td align="center">370</td>
<td align="center">370</td>
<td align="center">370</td>
<td align="center">370</td>
<td align="center">225</td>
<td align="center">240</td>
<td align="center">Demeso</td>
<td align="center">Demeso</td>
<td align="center">None</td>
<td align="center">None</td>
</tr>
<tr>
<td align="left">Leotiomycetes</td>
<td align="left">Helotiales</td>
<td align="center">370</td>
<td align="center">370</td>
<td align="center">370</td>
<td align="center">370</td>
<td align="center">340</td>
<td align="center">340</td>
<td align="center">340</td>
<td align="center">Macro/250</td>
<td align="center">None</td>
<td align="center">None</td>
</tr>
<tr>
<td align="left">Saccharomycetes</td>
<td align="left">Saccharomycetales</td>
<td align="center">500</td>
<td align="center">500</td>
<td align="center">500</td>
<td align="center">500</td>
<td align="center">500</td>
<td align="center">500</td>
<td align="center">500</td>
<td align="center">500</td>
<td align="center">Demacro/none/250</td>
<td align="center">None</td>
</tr>
<tr>
<td></td>
<td align="left">Schizosaccharomycetales</td>
<td align="center">650</td>
<td align="center">650</td>
<td align="center">650</td>
<td align="center">650</td>
<td align="center">650</td>
<td align="center">650</td>
<td align="center">650</td>
<td align="center">650</td>
<td align="center">650</td>
<td align="center">Demacro/none/240</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>Whole-genome synteny, indicated above the diagonal, was classified as either macrosynteny (macro), degraded macrosynteny (demacro), mesosynteny (meso), degraded mesosynteny (demeso) or no synteny (none). 'NA' indicates lack of sufficient data to perform whole-genome comparisons. Time since divergence between orders, previously predicted within the Ascomycetes [
<xref ref-type="bibr" rid="B38">38</xref>
], is indicated below the diagonal in millions of years.</p>
</table-wrap-foot>
</table-wrap>
<p>The number of sequenced fungal genomes has increased dramatically since 2008. There is now a sufficient number of sequenced species within each fungal class to begin to assess whole-genome patterns of evolution. In this paper, we have applied a simple dot-plot approach to fungal genome comparisons and observed a striking pattern of chromosome-level evolutionary conservation. This pattern is characterized by the conservation of gene content in chromosomes, without conservation of gene order or orientation; that is, synteny without co-linearity. We propose to call this sequence conservation 'mesosynteny' to distinguish it from micro- and macrosynteny. Mesosynteny appears to be peculiar to the filamentous Ascomycetes (syn. Pezizomycotina), particularly in the class Dothideomycetes. This phenomenon has interesting implications for the study of genome evolution and may have applications in the sequencing and assembly of fungal genomes.</p>
</sec>
<sec>
<title>Results</title>
<p>Dot plots are a well-established method of representing sequence comparisons [
<xref ref-type="bibr" rid="B26">26</xref>
]. Comparison of co-linear genomes (Supplementary Figure S1a in Additional file
<xref ref-type="supplementary-material" rid="S1">1</xref>
) gives a series of dots that lie on the diagonal (Supplementary Figure S1b in Additional file
<xref ref-type="supplementary-material" rid="S1">1</xref>
). Random gene loss from either chromosome without major rearrangements (Supplementary Figure S1c, d in Additional file
<xref ref-type="supplementary-material" rid="S1">1</xref>
) progressively destroys microsynteny but retains macrosynteny. Inversions are visualised on dot plots by diagonal lines with the opposite slope, while translocations are indicated when the genes on a chromosome of one species share syntenic blocks with two or more chromosomes. Conservation of short, contiguous runs of genes, whether on the same or different chromosomes, retains microsynteny but not macrosynteny.</p>
<p>The fungus
<italic>Phaeosphaeria </italic>
(syn.
<italic>Stagonospora</italic>
,
<italic>Septoria</italic>
)
<italic>nodorum </italic>
is a major pathogen of wheat [
<xref ref-type="bibr" rid="B27">27</xref>
]. It is a member of the class Dothideomycetes (Figure
<xref ref-type="fig" rid="F1">1</xref>
), a taxon that includes more than 20,000 species amongst which are many dominant crop pathogens [
<xref ref-type="bibr" rid="B28">28</xref>
]. Its genome, which is believed to comprise 14 to 19 chromosomes [
<xref ref-type="bibr" rid="B29">29</xref>
], was assembled as 107 nuclear scaffolds [
<xref ref-type="bibr" rid="B21">21</xref>
]. Expressed sequence tag and proteomic data have refined the annotations to a set of 12,194 genes [
<xref ref-type="bibr" rid="B30">30</xref>
-
<xref ref-type="bibr" rid="B32">32</xref>
]. Pathogenicity in
<italic>P. nodorum </italic>
has been linked to the expression of a suite of necrotrophic effectors [
<xref ref-type="bibr" rid="B33">33</xref>
-
<xref ref-type="bibr" rid="B36">36</xref>
] (formerly called host-specific toxins), some of which appear to have been acquired by lateral gene transfer [
<xref ref-type="bibr" rid="B14">14</xref>
,
<xref ref-type="bibr" rid="B16">16</xref>
].</p>
<p>The genome sequences of other Dothideomycetes species have become available recently, allowing whole-genome comparisons with relatively closely related taxa. We used the software tool MUMmer [
<xref ref-type="bibr" rid="B37">37</xref>
] to generate dot plots that compare the scaffolds of the
<italic>P. nodorum </italic>
assembly with the 21 finished chromosomes of
<italic>Mycosphaerella graminicola </italic>
[
<xref ref-type="bibr" rid="B38">38</xref>
,
<xref ref-type="bibr" rid="B39">39</xref>
] (Figure
<xref ref-type="fig" rid="F2">2a</xref>
). These species are classified respectively in the Pleosporales and the Capnodiales, order-level taxa within the Dothideomycetes (Figure
<xref ref-type="fig" rid="F2">2</xref>
), with an estimated divergence time of (very approximately) 300 million years ago (Mya). The figure is arranged with the chromosomes or scaffolds of each species arranged in size order along the axes. Dots correspond to regions of sequence similarity and are color-coded to indicate their degree of identity.</p>
<fig id="F2" position="float">
<label>Figure 2</label>
<caption>
<p>
<bold>Whole-genome dot-plot comparison between the Dothideomycetes species
<italic>Mycosphaerella graminicola </italic>
and
<italic>Phaeosphaeria nodorum</italic>
</bold>
.
<bold>(a) </bold>
The six-frame translations of both genomes were compared via MUMmer 3.0. Homologous regions are plotted as dots, which are color coded for percent similarity as per the color bar (right). Chromosomes 1 to 21 from
<italic>M. graminicola </italic>
are displayed by decreasing size along the y axis and scaffolds 1 to 107 from
<italic>P. nodorum </italic>
are displayed along the x axis. Dots represent matching regions between translated scaffold sequences. Mesosyntenic regions appear as dots within boxes without any obvious diagonal lines.
<bold>(b) </bold>
Homology relationships between chromosome 12 of
<italic>M. graminicola </italic>
and scaffold 17 of
<italic>P. nodorum</italic>
. Red lines link parallel homologous pairs and blue lines link anti-parallel pairs.</p>
</caption>
<graphic xlink:href="gb-2011-12-5-r45-2"></graphic>
</fig>
<p>Our expectation was that we would see either dispersed diagonal lines or a completely random distribution of very short matches ('dots'). Instead, the dot plot shows a highly non-random distribution whereby dots from individual chromosomes of
<italic>M. graminicola </italic>
appear to be strongly associated with one or a few scaffolds of
<italic>P. nodorum</italic>
, indicated by 'boxes' within columns and rows. For example, dots corresponding to
<italic>P. nodorum </italic>
scaffold 7 were almost exclusively found within the box corresponding to
<italic>M. graminicola </italic>
chromosome 12. Reciprocally, dots corresponding to
<italic>M. graminicola </italic>
chromosome 12 appeared predominantly within the box corresponding to
<italic>P. nodorum </italic>
scaffold 7. The dots within this box did not fall on any obvious diagonal lines and were instead arranged quasi-randomly. When these two sequences were aligned (Figure
<xref ref-type="fig" rid="F2">2b</xref>
), lines joining regions of significant similarity were distributed quasi-randomly. The orientation of the genes (color coded as red for parallel and blue for inverted) also appeared to be random. The dot plots used six-frame back translations of the genomes. Similar results were obtained with raw nucleotide sequences or when validated genes were used (Additional file
<xref ref-type="supplementary-material" rid="S2">2</xref>
). This indicated that the majority of the dots corresponded to genes.</p>
<p>We call this pattern of dots-within-boxes 'mesosynteny'. The non-random distribution implies conservation of the gene content of scaffolds (and by implication, chromosomes) during evolution; hence, this is a form of synteny [
<xref ref-type="bibr" rid="B40">40</xref>
] that does not involve the retention of co-linearity as found in both macro- and microsynteny.</p>
<sec>
<title>Taxonomic distribution of mesosynteny across the fungal kingdom</title>
<p>To test the extent and generality of mesosynteny within the fungi, the analysis was extended to other species within the Dothideomycetes, other classes within the Pezizomycotina and other fungal phyla. These comparisons were tested for chromosomal-scale genome conservation and were classified as macrosyntenic, mesosyntenic, or non-syntenic (Figure
<xref ref-type="fig" rid="F3">3</xref>
; Additional file
<xref ref-type="supplementary-material" rid="S3">3</xref>
).</p>
<fig id="F3" position="float">
<label>Figure 3</label>
<caption>
<p>
<bold>The whole-genome synteny classification process</bold>
. Genome sequences of fewer than 500 kb were discarded before analysis. The results of MUMmer comparisons between a pair of genomes were tested for synteny (see Materials and methods). If a genome pair was determined to be syntenic at a whole-genome level, synteny was classified as 'mesosyntenic' or 'macrosyntenic' based on the average length of co-linear diagonals.</p>
</caption>
<graphic xlink:href="gb-2011-12-5-r45-3"></graphic>
</fig>
<p>Visual inspection of dot plots distinguished the comparisons neatly into three classes: no synteny, macrosynteny or mesosynteny. Quantifying the degree of synteny between species required the development of new statistical tests. Significant sequence conservation was tested between pairs of scaffolds by a one-tailed cumulative binomial test, requiring a probability of ≥0.99. The whole-genome conservation was defined as significant when ≥25% of the expected number of scaffold pairs (assuming perfect whole-genome synteny) were conserved. Species pairs showing synteny were classified as macro- or mesosynteny based on the average length of co-linear runs of sequence matches between both genomes; an average co-linear diagonal length of ≥20 kb was considered macrosyteny and < 20 kb was classified as mesosynteny (Additional file
<xref ref-type="supplementary-material" rid="S3">3</xref>
). Mesosynteny and macrosynteny were further categorized into 'degraded' or 'non-degraded' (Figure
<xref ref-type="fig" rid="F3">3</xref>
). Synteny was classified as degraded when significant clusters of 'dots' or 'lines' were found outside of the primary box (that is, for any given 'box', < 75% of the total length of conserved sequences within its corresponding rows and columns resided within the dominant box). Scaffolds shorter than 500 kb were excluded from these analyses.</p>
<p>Dot-plot comparisons between the Dothideomycetes species
<italic>P. nodorum</italic>
,
<italic>M. graminicola</italic>
,
<italic>Mycosphaerella fijiensis </italic>
and
<italic>Leptosphaeria maculans </italic>
showed significant mesosynteny (Figure
<xref ref-type="fig" rid="F4">4</xref>
). The comparison between
<italic>P. nodorum </italic>
and
<italic>L. maculans </italic>
(both in the order Pleosporales) was especially striking (Additional file
<xref ref-type="supplementary-material" rid="S2">2</xref>
). The dot plot was dominated by matches of 80 to 100% similarity, compared to 60 to 80% in the case of
<italic>P. nodorum </italic>
versus the species in the Capnodiales,
<italic>M. graminicola </italic>
or
<italic>M. fijiensis</italic>
. The dots in the comparison between
<italic>P. nodorum </italic>
and
<italic>L. maculans </italic>
were almost exclusively restricted to single boxes within both rows and columns. As before, there was no indication of the diagonal lines characteristic of macrosynteny. This pattern of nearly exclusive dots within single boxes was also observed when comparisons were made between these genomes and the other released but so far unpublished Dothideomycetes genomes available via the JGI and Broad Institute web sites ([
<xref ref-type="bibr" rid="B39">39</xref>
,
<xref ref-type="bibr" rid="B41">41</xref>
,
<xref ref-type="bibr" rid="B42">42</xref>
] and data not shown).</p>
<fig id="F4" position="float">
<label>Figure 4</label>
<caption>
<p>
<bold>Dot-plot comparisons between the class Dothideomycetes and related classes</bold>
. Scaffolds greater than 500 kb in length are ordered in ascending alpha-numeric order upwards along the y-axis and left-to-right along the x-axis. The orders Pleosporales (represented by
<italic>P. nodorum </italic>
and
<italic>L. maculans</italic>
) and Capnodiales (
<italic>Mycosphaerella </italic>
spp.) of the Dothideomycetes exhibit a tightly clustered pattern of mesosynteny between and within each order. This degrades into a mesosynteny-like pattern in comparisons between Dothideomycetes and the classes Eurotiomycetes (
<italic>A. fumigatus</italic>
), Sordariomycetes (
<italic>M. oryzae</italic>
) and Leotiomycetes (
<italic>S. sclerotiorum</italic>
). Clustered blocks can still be observed in these comparisons. The dot-plots comparing Dothideomycetes and Saccharomycetes (
<italic>S. cerevisiae</italic>
) appear to be random - that is, there was no synteny.</p>
</caption>
<graphic xlink:href="gb-2011-12-5-r45-4"></graphic>
</fig>
<p>Dothideomycetes species also showed a discernable level of mesosynteny-like conservation with species representing the classes Eurotiomycetes (
<italic>Aspergillus fumigatus</italic>
), and the Leotiomycetes (
<italic>Sclerotinia sclerotiorum</italic>
;
<italic>S. sclerotiorum </italic>
sequencing project [
<xref ref-type="bibr" rid="B43">43</xref>
]), but not with the Sordariomycetes (
<italic>Magnaporthe oryzae</italic>
) or the Saccharomycetes (
<italic>Saccharomyces cerevisiae</italic>
) (Figure
<xref ref-type="fig" rid="F4">4</xref>
; Additional file
<xref ref-type="supplementary-material" rid="S1">1</xref>
). Comparisons of
<italic>P. nodorum </italic>
and
<italic>M. graminicola </italic>
with
<italic>A. fumigatus </italic>
and
<italic>S. sclerotiorum </italic>
had a statistically significant non-random distribution of dots within boxes. In contrast to intra-Dothideomycetes comparisons, dots appeared in multiple boxes within a row and column. This is an example of degraded mesosynteny. Comparisons between Dothideomycetes and
<italic>M. oryzae </italic>
(Sordariomycetes) and the yeast
<italic>S. cerevisiae </italic>
(Saccharomycetes) failed to find a statistically significant degree of synteny, reflected in the apparently random distribution of dots. These comparisons had an average of 1 and 0 sequences with binomial probabilities of significant sequence conservation >0.99. No statistically significant syntenic relationships were found when either
<italic>M. oryzae </italic>
or any yeast was compared with other filamentous fungal genomes.</p>
<p>A similar series of dot-plot comparisons between the class Eurotiomycetes and Leotiomycetes and species from classes of the Ascomycota is shown in Figure
<xref ref-type="fig" rid="F5">5</xref>
. The test species are
<italic>A. fumigatus </italic>
and
<italic>S. sclerotiorum</italic>
. The comparisons between
<italic>S. sclerotiorum </italic>
and
<italic>Botryotinia fuckeliana </italic>
exhibited a highly conserved pattern with many obvious diagonal lines made up of red and yellow dots representing highly similar (90 to 100%) sequence pairs. The average length of co-linear regions was much greater than 20 kb. This is a classical macrosyntenic pattern reflecting very recent divergence between these closely related genera. A weaker macrosyntenic pattern was observed between
<italic>A. fumigatus </italic>
and
<italic>Penicillium marneffei</italic>
, two species in the Eurotiales. Less than 25% of matches in columns and rows resided within a single box, characteristic of degraded macrosynteny. Comparisons between
<italic>A. fumigatus </italic>
and
<italic>S. sclerotiorum </italic>
and the Dothideomycetes, represented by
<italic>L. maculans</italic>
, revealed degraded mesosynteny. This was also observed between
<italic>S. sclerotiorum </italic>
and the two members of the Eurotiales,
<italic>A. fumigatus </italic>
and
<italic>P. marneffei</italic>
.</p>
<fig id="F5" position="float">
<label>Figure 5</label>
<caption>
<p>
<bold>Dot-plot comparisons between representatives of the classes Eurotiomycetes and Leotiomycetes and related classes</bold>
. The orders Eurotiales (
<italic>Aspergillus </italic>
spp.) and Onygenales (
<italic>P. marneffei</italic>
) of the Eurotiomycetes exhibit degraded macrosynteny between and within each order. The Leotiomycetes exhibit macrosynteny between species of the order Helotiales. A mesosynteny-like pattern is observed in comparisons between the Eurotiomycetes, Leotiomycetes and the more distantly related class Dothideomycetes (
<italic>L. maculans</italic>
).</p>
</caption>
<graphic xlink:href="gb-2011-12-5-r45-5"></graphic>
</fig>
<p>The Sordariomycetes
<italic>Fusarium oxysporum </italic>
exhibited mixed patterns of synteny in comparisons between species from the related orders Sordariales and Hypocreales and from other classes in the Pezizomycotina (Figure
<xref ref-type="fig" rid="F6">6</xref>
; Additional file
<xref ref-type="supplementary-material" rid="S4">4</xref>
). Striking macrosynteny was observed between chromosomes 1, 2, 4, 5 and 7 to 10 of
<italic>F. oxysporum </italic>
and chromosomes 1 to 6 and 7 to 10 of
<italic>Nectria haematococca</italic>
. Parts of chromosomes 3, 6 and 11 to 14 of
<italic>F. oxysporum </italic>
exhibited a mesosyntenic pattern with chromosomes 7 and 11 to 14 of
<italic>N. haematococca</italic>
. Mesosynteny was strongest between
<italic>N. haematococca </italic>
chromosome 14 and parts of
<italic>F. oxysporum </italic>
chromosomes 3, 6, 14 and 15. Degraded mesosynteny was observed between
<italic>F. oxysporum </italic>
and
<italic>Neurospora crassa</italic>
,
<italic>S. sclerotiorum</italic>
,
<italic>A. fumigatus </italic>
and with
<italic>P. nodorum</italic>
. However, in all comparisons (excluding
<italic>N. haematococca</italic>
), dots were conspicuously absent from rows corresponding to
<italic>F. oxysporum </italic>
chromosomes 3, 6, 14 and 15 (Figure
<xref ref-type="fig" rid="F6">6</xref>
).</p>
<fig id="F6" position="float">
<label>Figure 6</label>
<caption>
<p>
<bold>Dot-plot comparisons between two members of the class Sordariomycetes and related classes</bold>
. The orders Sordariales (
<italic>N</italic>
. crassa and
<italic>P. anserina</italic>
) and Hypocreales (
<italic>F. oxysporum </italic>
and
<italic>N. haematococca</italic>
) of the Sordariomycetes generally exhibit mesosynteny-like conservation. The closely related pair of Hypocreales species
<italic>Fusarium oxysporum </italic>
and
<italic>Nectria haematococca </italic>
exhibit mostly macrosynteny with mesosynteny between a few chromosomes. Comparisons between the Sordariales and Hypocreales with the classes Leotiomycetes, Eurotiomycetes and Dothideomycetes exhibit degraded mesosynteny. Lack of synteny between the conditionally dispensable chromosomes 3, 6, 14 and 15 of
<italic>F. oxysporum </italic>
(excluding
<italic>N. haematococca</italic>
) with chromosomes of any other species is evident by an absence of dots in those comparisons.</p>
</caption>
<graphic xlink:href="gb-2011-12-5-r45-6"></graphic>
</fig>
<p>The comparison between
<italic>N. crassa </italic>
and
<italic>Podospora anserina </italic>
(order Sordariales) showed a dominant pattern of mesosynteny, with some macrosyntenic regions particularly between the largest chromosome of both species [
<xref ref-type="bibr" rid="B20">20</xref>
].
<italic>N. crassa </italic>
exhibited degraded mesosynteny when compared to
<italic>S. sclerotiorum</italic>
,
<italic>A. fumigatus </italic>
and
<italic>P. nodorum </italic>
(Figure
<xref ref-type="fig" rid="F6">6</xref>
).</p>
<p>We expanded these comparisons beyond the classes presented above to include additional species of the sub-phyla Saccharomycotina and Taphrinomycotina within the phylum Ascomycota and species from the phyla Basidiomycota, Blastocladiomycota and Chytridiomycota (Table
<xref ref-type="table" rid="T1">1</xref>
; Figure
<xref ref-type="fig" rid="F1">1</xref>
). Non-filamentous Ascomycetes (classes Saccharomycetes and Schizosaccharomycetes) exhibited either macrosynteny or no synteny within their respective classes and no synteny with other fungal classes (Additional file
<xref ref-type="supplementary-material" rid="S5">5</xref>
). The class Agaricomycetes exhibited degraded macrosynteny between species within the class and no synteny with other fungal classes (Additional file
<xref ref-type="supplementary-material" rid="S6">6</xref>
). No non-Pezizomycotina taxa showed any level of synteny when compared to species of a different class (Table
<xref ref-type="table" rid="T1">1</xref>
; Additional file
<xref ref-type="supplementary-material" rid="S1">1</xref>
).</p>
</sec>
</sec>
<sec>
<title>Discussion</title>
<p>A novel and unexpected mode of chromosome-level sequence conservation, which we have called mesosynteny, has been detected between species of filamentous Ascomycetes, and in particular the Dothideomycetes. Mesosynteny implies the conservation of gene content within chromosomes but without conservation of gene order or orientation. It contrasts markedly with the macrosynteny observed commonly in plants and animals and the absence of synteny seen in other eukaryotes such as distantly related yeast species. The cause of mesosyntenic chromosomal evolution is not known. However, a mesosyntenic pattern would be expected to occur if intra-chromosomal recombination (including inversions) occurred significantly more frequently than inter-chromosomal recombinational events such as translocations.</p>
<p>Mesosynteny is distinct from macrosynteny. Macrosynteny would be expected to arise when the predominant modes of chromosomal evolution are inter-chromosomal recombination and gene loss. These considerations suggest that different patterns of mutagenic events can lead either to mesosynteny or to macrosynteny as chromosomes evolve following a speciation event.</p>
<p>Mesosynteny also is distinct from microsynteny, which is characterized by co-linearity between clusters of two to about ten genes with both order and orientation conserved. Earlier comparisons of synteny in related filamentous fungi frequently found clusters of genes with related functions but without retention of gene order or orientation. An example is the quinate cluster, which is conserved across species of the Ascomycetes [
<xref ref-type="bibr" rid="B21">21</xref>
,
<xref ref-type="bibr" rid="B44">44</xref>
]. This pattern of shuffled cluster retention is akin to what we observe at the whole-chromosome level.</p>
<p>Our results suggest that mesosyntenic chromosomal conservation is restricted to the Pezizomycotina and is most pronounced in the Dothideomycetes [
<xref ref-type="bibr" rid="B45">45</xref>
]. The Dothideomycetes are the only group to exhibit non-degraded mesosynteny between species of the different genera (estimated to have diverged approximately 120 to 150 Mya) and orders (approximately 300 Mya). A recognizable yet degraded form of mesosynteny was found between many species of Pezizomycotina outside the Dothideomycetes. The estimated time of divergence within Dothideomycetes orders are comparable to other orders within the Pezizomycotina that exhibited either degraded mesosynteny or no detectable synteny (Table
<xref ref-type="table" rid="T1">1</xref>
) [
<xref ref-type="bibr" rid="B38">38</xref>
]. No mesosynteny was observed in any of the fungal groups outside of the Pezizomycotina that were surveyed: yeasts, Basidiomycetes, Blastocladiomycetes and Chytridiomycetes. The evolutionary separation between these groups and the Dothideomycetes (500 to 650 Mya) [
<xref ref-type="bibr" rid="B38">38</xref>
] may be so great that both mesosynteny and macrosynteny have decayed below the limit of detection. To our knowledge, mesosynteny has not been observed in non-fungal eukaryotes. Superficially similar dot-plots have been occasionally observed in comparisons of chordate genomes [
<xref ref-type="bibr" rid="B45">45</xref>
] but appear to be due to the amplification of paralogous copies of genes within chromosomes. Overall, either macrosynteny or no synteny has been found outside the Pezizomycotina.</p>
<p>Chromosomal conservation akin to mesosynteny had been observed previously in a number of inter-species comparisons within the Pezizomycotina, but its full extent was not analyzed. These include comparisons between the Pezizomycetes
<italic>Tuber melanosporum </italic>
and the Eurotiomycetes
<italic>Coccidioides immitus </italic>
[
<xref ref-type="bibr" rid="B46">46</xref>
] and the Sordariomycetes
<italic>P. anserina </italic>
and
<italic>N. crassa </italic>
[
<xref ref-type="bibr" rid="B20">20</xref>
]. As
<italic>N. crassa </italic>
and
<italic>P. anserina </italic>
are heterothallic, the authors suggested that the observed conservation may be specific to out-crossing (heterothallic) fungi. However, evidence from this study suggests otherwise as mesosynteny was observed between both heterothallic and homothallic species (Table
<xref ref-type="table" rid="T1">1</xref>
; Additional files
<xref ref-type="supplementary-material" rid="S3">3</xref>
and
<xref ref-type="supplementary-material" rid="S5">5</xref>
). For example, two homothallic Sordariomycetes species, which diverged approximately 225 Mya [
<xref ref-type="bibr" rid="B38">38</xref>
], exhibited degraded mesosynteny (
<italic>Fusarium graminearum </italic>
and
<italic>Chaetomium globosum</italic>
; Additional file
<xref ref-type="supplementary-material" rid="S7">7</xref>
).</p>
<p>Mesosynteny was observed in species both with and without (
<italic>F. oxysporum </italic>
[
<xref ref-type="bibr" rid="B47">47</xref>
] and
<italic>Penicillium marneffei </italic>
[
<xref ref-type="bibr" rid="B48">48</xref>
]) a known sexual stage. It may be that sexual crossing has been lost relatively recently in these species. Nonetheless, this finding suggests that mesosyntenic relationships were not quickly lost in the absence of meiosis. Amongst the mesosyntenic Pezizomycotina, mesosynteny was weakest in comparisons against the
<italic>M. oryzae </italic>
genome (Figures
<xref ref-type="fig" rid="F5">5</xref>
and
<xref ref-type="fig" rid="F6">6</xref>
; Table
<xref ref-type="table" rid="T1">1</xref>
).
<italic>M. oryzae </italic>
is believed to exist in nature in purely asexual lineages. The sequenced isolate of
<italic>M. oryzae </italic>
was a fertile derivative of two asexual lineages [
<xref ref-type="bibr" rid="B19">19</xref>
]. We speculate that a history of asexual reproduction and/or the process of laboratory domestication may have destroyed the remnants of mesosynteny in this isolate. This hypothesis could be tested by comparisons with genome sequences from additional isolates of
<italic>M. oryzae </italic>
or related species in the Magnaporthales.</p>
<p>In some species there was an uneven distribution of syntenic relationships between different chromosomes. The genome of
<italic>M. graminicola </italic>
has been finished [
<xref ref-type="bibr" rid="B39">39</xref>
] and comprises 21 chromosomes, the eight smallest of which have been shown to be dispensable [
<xref ref-type="bibr" rid="B49">49</xref>
]. These dispensable chromosomes displayed little sequence conservation with genes from any other species, and therefore no detectable synteny of any type (Figure
<xref ref-type="fig" rid="F4">4</xref>
). In contrast, the
<italic>M. graminicola </italic>
core chromosomes exhibited a typical mesosyntenic pattern in most comparisons with other Pezizomycotina species. Similarly, the conditionally dispensable chromosomes (CDCs) of
<italic>F. oxysporum </italic>
(3, 6, 14 and 15) showed no synteny with almost all species tested. All of these supernumerary chromosomes are thought to have originated by lateral transfer from unknown donor species [
<xref ref-type="bibr" rid="B39">39</xref>
,
<xref ref-type="bibr" rid="B50">50</xref>
]. Whether the lack of synteny of most supernumerary chromosomes is because they come from distantly related species or because they evolve more rapidly than core chromosomes is not known.</p>
<p>Surprisingly, CDC 14 of
<italic>N. haematococca </italic>
was mesosyntenic to
<italic>F. oxysporum </italic>
CDCs (chromosome 14 and the terminal end of chromosomes 3 and 6; Figure
<xref ref-type="fig" rid="F6">6</xref>
; Additional file
<xref ref-type="supplementary-material" rid="S4">4</xref>
). This is in contrast to the core chromosomes of each species, which exhibited macrosynteny and to previous comparisons that had indicated that these CDCs were non-syntenic. A comparison of the
<italic>F. oxysporum </italic>
genome with the closely related
<italic>Fusarium verticillioides </italic>
indicated that the
<italic>F. oxysporum </italic>
CDCs were not syntenic [
<xref ref-type="bibr" rid="B50">50</xref>
]. A possible explanation for this phenomenon is that mutations and rearrangements in supernumerary chromosomes accumulate more rapidly because these chromosomes are rarely required for survival. Faster accumulation of mutations potentially coupled with origins in distantly related donor species may allow the sequences of supernumerary chromosomes to diverge to the point where no sequence similarity remains (as in
<italic>M. graminicola</italic>
). The occurrence of mesosyntenic rearrangement in
<italic>F. oxysporum </italic>
and
<italic>N. haematococca </italic>
may also be related to the origin of their CDCs. These may have arisen in their common ancestor from a single chromosome, which subsequently mutated and broke into smaller chromosomes. Alternatively, they may have been recently transferred laterally from a common (or closely related) donor.</p>
<p>Whole-genome shotgun sequencing involves the generation of many short DNA reads that are assembled into longer segments. Macrosyntenic relationships are commonly used to assist the assembly and finishing of fragmented genome sequences, particularly in prokaryotic genomes. Sequences that are macrosyntenic to a long sequence of a closely related genome can be confidently hypothesized to be joined physically. Mesosynteny between a new genome assembly with a reference genome also may be used to suggest which scaffolds are juxtaposed. This could significantly reduce the cost and complexity of assembling and finishing genomes. To test whether mesosynteny could be used to predict scaffold joins in genomic sequences, early and late assemblies of the
<italic>M. graminicola </italic>
genome were analyzed to determine whether the joining of contigs or scaffolds in the finished genome could have been predicted by mesosyntenic relationships of the draft genome to
<italic>P. nodorum </italic>
[
<xref ref-type="bibr" rid="B39">39</xref>
]. Mesosynteny was remarkably successful in predicting separate scaffolds that should be joined and for identifying mis-joins in the initial assembly. This approach has the potential to assist with assembly and finishing of other genomes within the Pezizomycotina.</p>
</sec>
<sec>
<title>Conclusions</title>
<p>We have unearthed a novel mode of evolution in which chromosomes retain their content but shuffle the order and orientation of genes. We propose to call this phenomenon mesosynteny. What is the origin and mechanism of mesosynteny? The phenomenon is observed only in the Pezizomycotina and especially in the Dothideomycetes. The Dothideomycetes sequenced to date have several (ten or more) relatively small chromosomes, hinting at the ubiquity of supernumerary chromosomes within this taxon. The Pezizomycotina exhibit repeat-induced point mutation and higher frequencies of lateral gene transfer compared to other fungi [
<xref ref-type="bibr" rid="B15">15</xref>
,
<xref ref-type="bibr" rid="B51">51</xref>
]. Are these phenomena causally related?</p>
<p>The mechanism for mesosynteny may occur through a high frequency of inversions during meiosis. Whether the Dothideomycetes have a higher propensity for inversions is not known but should be the subject of further investigation. Alternatively, lateral gene transfer may be the driving force behind mesosynteny. The mechanism of lateral gene transfer is not well understood, but recent evidence suggests that the sequence transferred can be very large, even up to the size of entire chromosomes [
<xref ref-type="bibr" rid="B49">49</xref>
,
<xref ref-type="bibr" rid="B52">52</xref>
]. Fungi are capable of fusing with other fungal species through either conidial or hyphal anastomosis tubes [
<xref ref-type="bibr" rid="B53">53</xref>
]. Fusion can lead to exchange of nuclei and the transient formation of heterkaryotic strains. If the transferred DNA carried a gene that was beneficial to the recipient species, the chromosome (or a large section) carrying this gene may be retained whilst other donated chromosomes would be lost. As mesosynteny tends to retain genes on the same chromosomes, a recipient species may be able to accept a substitute chromosome from a reasonably closely related species without major disruption of phenotype. Recombination between the new and old chromosome would shuffle the order and orientation of genes, with remnant duplicated genes being removed in further cycles of repeat-induced point mutation. Recombinants with a complete core gene content plus any advantageous laterally transferred genes would then be selected, resulting in the mesosyntenic pattern of chromosomal conservation we see today. Mesosynteny may, therefore, be an adaptive mechanism that both allowed and resulted from lateral acquisition of large chromosomal sections.</p>
</sec>
<sec sec-type="materials|methods">
<title>Materials and methods</title>
<sec>
<title>Whole-genome comparisons</title>
<p>The synteny classification method is outlined in Figure
<xref ref-type="fig" rid="F3">3</xref>
. Genome sequence assemblies of the species listed in Figure
<xref ref-type="fig" rid="F1">1</xref>
were obtained from the sources described in Additional file
<xref ref-type="supplementary-material" rid="S1">1</xref>
. Phylogenetic data (Figure
<xref ref-type="fig" rid="F1">1</xref>
; Table
<xref ref-type="table" rid="T1">1</xref>
) were inferred from previous publications [
<xref ref-type="bibr" rid="B1">1</xref>
,
<xref ref-type="bibr" rid="B28">28</xref>
,
<xref ref-type="bibr" rid="B54">54</xref>
,
<xref ref-type="bibr" rid="B55">55</xref>
]. Individual sequences (contigs, scaffolds or chromosomes) less than 500 kbp in length were discarded from the analysis. Whole-genome comparisons were performed using promer (MUMmer 3.0, [
<xref ref-type="bibr" rid="B37">37</xref>
]) with the '--mum' parameter. Promer outputs were filtered for repetitive matches using the program 'delta-filter' (MUMmer 3.0) with the '-g' parameter. Genome dot plots were generated using 'mummerplot' (MUMmer 3.0) and coordinates of promer matches were derived from filtered promer outputs using the 'show-coords' program (MUMmer 3.0).</p>
</sec>
<sec>
<title>Determination of significant sequence conservation</title>
<p>For the purposes of this study, only synteny observable at a whole-genome level was considered. For a given pair of genomes (genome A and genome B), all combinations of their sequence (contigs, scaffolds or chromosomes) pairs (one sequence from genome A (sequence A) and one from genome B (sequence B)) were tested for significant conservation. Lengths of conserved regions in sequences A and B were derived from MUMmer outputs. The probability of synteny (P
<sub>syn</sub>
) for sequence pairs was calculated via a one-tailed cumulative binomial test:
<disp-formula>
<graphic xlink:href="gb-2011-12-5-r45-i1.gif"></graphic>
</disp-formula>
</p>
<p>where x = (Length conserved in sequence A × Length conserved in sequence B)/(Length of sequence A × Length of sequence B);
<italic>n </italic>
= 100; p = (Total length conserved in Genome A × Total length conserved in Genome B)/(Total length genome A × Total length genome B). P
<sub>syn </sub>
was required to be ≥ 0.99 to indicate significant amounts of sequence conservation between a sequence pair.</p>
</sec>
<sec>
<title>Analysis of syntenic regions between conserved sequences</title>
<p>The lengths of syntenic regions were analyzed for significantly conserved sequence pairs. Extended co-linearity of sequence matches visible as uninterrupted diagonal lines on a dot plot was used as an indicator of macrosynteny (Additional file
<xref ref-type="supplementary-material" rid="S1">1</xref>
). Dot plots between sequence pairs were considered as individual scatter plots. Promer matches between a pair of sequences were converted into a series of points on the scatter plot, with a point added every 1 kb along each match. R
<sup>2 </sup>
values were calculated along the axis of sequence A in 20-kb windows (incrementing along by 2 kb). A window was considered to be co-linear if it contained a minimum of 15 data points with an R
<sup>2 </sup>
≥ 0.9 The end coordinates of co-linear windows were subsequently modified to exclude the coordinate range of overlapping non-co-linear windows. The data points of co-linear windows within 50 kb of one another were combined (including intermediate data points if not overlapping) and were merged into larger co-linear windows if (Slope of window 1/Slope of window 2) > 0.8 and < 1.2. The start and end points of co-linear windows with a length of ≥ 5 kb were used as the coordinates of 'syntenic regions'. The same process was repeated along the axis of sequence B.</p>
</sec>
<sec>
<title>Classification of synteny type</title>
<p>Whole-genome synteny was identified by the 'significant pair ratio' statistic, which is an indicator of the proportion of conserved sequences relative to the expected number of conserved sequences. The significant pair ratio was determined by:
<disp-formula>
<graphic xlink:href="gb-2011-12-5-r45-i2.gif"></graphic>
</disp-formula>
</p>
<p>where N
<sub>scp </sub>
is the number of significantly conserved pairs between genomes A and B; S
<sub>a </sub>
is the number of sequences in genome A ≥ 500 kb; and S
<sub>b </sub>
is the number of sequences in genome B ≥ 500 kb.</p>
<p>Whole-genome synteny was identified when the significant pair ratio was ≥ 0.25. Genome pairs failing this criterion were classified as 'non-syntenic'. Genome pairs passing the test for whole-genome synteny were sub-categorized as either macrosyntenic or mesosyntenic, defined by an average length of syntenic regions (combined between both compared genomes) of greater than or less than 20 kb, respectively. Synteny type was further categorized into 'degraded' or 'non-degraded' based on the statistic 'pair exclusivity'. For a given sequence pair, consisting of sequence A of genome A and sequence B of genome B, the 'pair exclusivity' was calculated by:
<disp-formula>
<graphic xlink:href="gb-2011-12-5-r45-i3.gif"></graphic>
</disp-formula>
</p>
<p>where C
<sub>ab </sub>
is the total length of conserved matches between sequences A and B; C
<sub>Ab </sub>
is the total length of conserved matches for sequence A and all sequences of genome B; and C
<sub>aB </sub>
is the total length of conserved matches for sequence B and all sequences of genome A.</p>
<p>Synteny was classified as 'degraded' if the maximum value of all pair exclusivities was less than 0.75.</p>
</sec>
</sec>
<sec>
<title>Abbreviations</title>
<p>CDC: conditionally dispensable chromosome; Mya: million years ago.</p>
</sec>
<sec>
<title>Authors' contributions</title>
<p>RPO and JKH conceived and designed the study. JKH developed algorithms and performed mesosynteny analyses. JKH and RPO wrote the manuscript. TR, BJH, GHJK and SBG contributed data. JKH, RPO, TR, BJH, GHJK and SBG edited the manuscript. All authors read and approved the final manuscript.</p>
</sec>
<sec sec-type="supplementary-material">
<title>Supplementary Material</title>
<supplementary-material content-type="local-data" id="S1">
<caption>
<title>Additional file 1</title>
<p>
<bold>Supplementary Figure S1</bold>
. The origins of the different types of syntenic relationships. Immediately after a speciation event, equivalent chromosomes in two daughter species retain the gene content, order and orientation of the parent species.
<bold>(a) </bold>
Diagrammatic representation of a chromosome with sequential elements A to Z.
<bold>(b) </bold>
A dot plot comparing the chromosomes in (a), with letters substituted for dots. The unbroken series of letters on the diagonal indicates macrosynteny.
<bold>(c, d) </bold>
Loss of sequences from each chromosome (c) will degrade the diagonal co-linearity when visualized as a dot plot (d).</p>
</caption>
<media xlink:href="gb-2011-12-5-r45-S1.PNG" mimetype="image" mime-subtype="png">
<caption>
<p>Click here for file</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="S2">
<caption>
<title>Additional file 2</title>
<p>
<bold>Supplementary Figure S2</bold>
.
<bold>(a, b) </bold>
Correspondence between promer-derived dot plots (a) and blastp-derived protein comparisons of annotated genes (b) between
<italic>Phaeosphaeria nodorum </italic>
and
<italic>Leptosphaeria maculans</italic>
. Sequence pairs ('boxes') in (a) containing non-random distributions of 'dots' correspond to those in (b), indicating that the back-translated genome matches in (a) correspond to regions of conserved gene content.</p>
</caption>
<media xlink:href="gb-2011-12-5-r45-S2.PNG" mimetype="image" mime-subtype="png">
<caption>
<p>Click here for file</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="S3">
<caption>
<title>Additional file 3</title>
<p>
<bold>Supplementary File 1</bold>
. Predictions of synteny between all species involved in this study in an Excel file.</p>
</caption>
<media xlink:href="gb-2011-12-5-r45-S3.XLS" mimetype="application" mime-subtype="vnd.ms-excel">
<caption>
<p>Click here for file</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="S4">
<caption>
<title>Additional file 4</title>
<p>
<bold>Supplementary Figure S3</bold>
. Presence of both macrosyntenic and mesosyntenic conservation patterns between the genomes of
<italic>Fusarium oxysporum </italic>
and
<italic>Nectria haematococca</italic>
. Core chromosomes (indicated by black bars along the axes) are macrosyntenic between the two species. Dispensable chromosomes (red bars along the axes) are either non-syntenic (
<italic>N. haematococca </italic>
chromosomes 15 to 17) or mesosyntenic (
<italic>N. haematococca </italic>
chromosomes 7 and 11 to 14,
<italic>F. oxysporum </italic>
chromosome 14). The majority of chromosomes 3 and 6 of
<italic>F. oxysporum </italic>
had no similarity to the chromosomes of
<italic>N. haematococca </italic>
except for regions near their telomeres.</p>
</caption>
<media xlink:href="gb-2011-12-5-r45-S4.PNG" mimetype="image" mime-subtype="png">
<caption>
<p>Click here for file</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="S5">
<caption>
<title>Additional file 5</title>
<p>
<bold>Supplementary Figure S4</bold>
. Degradation of whole-genome synteny in the classes Saccharomycetes and Schizosaccharomyces. Whole-genome dot plots have been limited to scaffolds or chromosomes greater than 500 kb. Species of the
<italic>Saccharomyces </italic>
and
<italic>Schizosaccharomyces </italic>
do not exhibit whole-genome conservation with each other. Certain species within each class exhibit macrosynteny whereas others exhibit no synteny.</p>
</caption>
<media xlink:href="gb-2011-12-5-r45-S5.PNG" mimetype="image" mime-subtype="png">
<caption>
<p>Click here for file</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="S6">
<caption>
<title>Additional file 6</title>
<p>
<bold>Supplementary Figure S5</bold>
. Degradation of whole-genome synteny between a member of the class Agaricales and related orders. Whole-genome dot plots have been limited to scaffolds or chromosomes greater than 500 kb. Species in the Agaricales exhibited macrosynteny with each other. However, the Agaricales exhibited no synteny with the closest related classes represented in this study, the Exobasidiomycetes and Pucciniomycetes.</p>
</caption>
<media xlink:href="gb-2011-12-5-r45-S6.PNG" mimetype="image" mime-subtype="png">
<caption>
<p>Click here for file</p>
</caption>
</media>
</supplementary-material>
<supplementary-material content-type="local-data" id="S7">
<caption>
<title>Additional file 7</title>
<p>
<bold>Supplementary Figure S6</bold>
. Evidence of degraded mesosynteny between the genomes of two homothallic Sordariomycete species,
<italic>Fusarium graminearum </italic>
(order Hypocreales) and
<italic>Chaetomium globosum </italic>
(order Sordariales). These two species are estimated to have diverged approximately 225 Mya. Sequence matches (dots) are arranged in blocked clusters typical of mesosynteny. Chromosomes and scaffolds do not share a one-to-one relationship, with multiple mesosyntenic clusters appearing in the same row or column.</p>
</caption>
<media xlink:href="gb-2011-12-5-r45-S7.PNG" mimetype="image" mime-subtype="png">
<caption>
<p>Click here for file</p>
</caption>
</media>
</supplementary-material>
</sec>
</body>
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