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Dynamics and evolution of the inverted repeat-large single copy junctions in the chloroplast genomes of monocots

Identifieur interne : 002057 ( Main/Exploration ); précédent : 002056; suivant : 002058

Dynamics and evolution of the inverted repeat-large single copy junctions in the chloroplast genomes of monocots

Auteurs : Rui-Jiang Wang [République populaire de Chine, Taïwan] ; Chiao-Lei Cheng [Taïwan] ; Ching-Chun Chang [Taïwan] ; Chun-Lin Wu [Taïwan] ; Tian-Mu Su [Taïwan] ; Shu-Miaw Chaw [Taïwan]

Source :

RBID : PMC:2275221

Abstract

Background

Various expansions or contractions of inverted repeats (IRs) in chloroplast genomes led to fluxes in the IR-LSC (large single copy) junctions. Previous studies revealed that some monocot IRs contain a trnH-rps19 gene cluster, and it has been speculated that this may be an evidence of a duplication event prior to the divergence of monocot lineages. Therefore, we compared the organizations of genes flanking two IR-LSC junctions in 123 angiosperm representatives to uncover the evolutionary dynamics of IR-LSC junctions in basal angiosperms and monocots.

Results

The organizations of genes flanking IR-LSC junctions in angiosperms can be classified into three types. Generally each IR of monocots contains a trnH-rps19 gene cluster near the IR-LSC junctions, which differs from those in non-monocot angiosperms. Moreover, IRs expanded more progressively in monocots than in non-monocot angiosperms. IR-LSC junctions commonly occurred at polyA tract or A-rich regions in angiosperms. Our RT-PCR assays indicate that in monocot IRA the trnH-rps19 gene cluster is regulated by two opposing promoters, S10A and psbA.

Conclusion

Two hypotheses are proposed to account for the evolution of IR expansions in monocots. Based on our observations, the inclusion of a trnH-rps19 cluster in majority of monocot IRs could be reasonably explained by the hypothesis that a DSB event first occurred at IRB and led to the expansion of IRs to trnH, followed by a successive DSB event within IRA and lead to the expansion of IRs to rps19 or to rpl22 so far. This implies that the duplication of trnH-rps19 gene cluster was prior to the diversification of extant monocot lineages. The duplicated trnH genes in the IRB of most monocots and non-monocot angiosperms have distinct fates, which are likely regulated by different expression levels of S10A and S10B promoters. Further study is needed to unravel the evolutionary significance of IR expansion in more recently diverged monocots.


Url:
DOI: 10.1186/1471-2148-8-36
PubMed: 18237435
PubMed Central: 2275221


Affiliations:


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Le document en format XML

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<title xml:lang="en" level="a" type="main">Dynamics and evolution of the inverted repeat-large single copy junctions in the chloroplast genomes of monocots</title>
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<name sortKey="Wang, Rui Jiang" sort="Wang, Rui Jiang" uniqKey="Wang R" first="Rui-Jiang" last="Wang">Rui-Jiang Wang</name>
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<title>Background</title>
<p>Various expansions or contractions of inverted repeats (IRs) in chloroplast genomes led to fluxes in the IR-LSC (large single copy) junctions. Previous studies revealed that some monocot IRs contain a
<italic>trnH-rps19 </italic>
gene cluster, and it has been speculated that this may be an evidence of a duplication event prior to the divergence of monocot lineages. Therefore, we compared the organizations of genes flanking two IR-LSC junctions in 123 angiosperm representatives to uncover the evolutionary dynamics of IR-LSC junctions in basal angiosperms and monocots.</p>
</sec>
<sec>
<title>Results</title>
<p>The organizations of genes flanking IR-LSC junctions in angiosperms can be classified into three types. Generally each IR of monocots contains a
<italic>trnH-rps19 </italic>
gene cluster near the IR-LSC junctions, which differs from those in non-monocot angiosperms. Moreover, IRs expanded more progressively in monocots than in non-monocot angiosperms. IR-LSC junctions commonly occurred at polyA tract or A-rich regions in angiosperms. Our RT-PCR assays indicate that in monocot IR
<sub>A </sub>
the
<italic>trnH-rps19 </italic>
gene cluster is regulated by two opposing promoters,
<italic>S10</italic>
<sub>
<italic>A </italic>
</sub>
and
<italic>psbA</italic>
.</p>
</sec>
<sec>
<title>Conclusion</title>
<p>Two hypotheses are proposed to account for the evolution of IR expansions in monocots. Based on our observations, the inclusion of a
<italic>trnH-rps19 </italic>
cluster in majority of monocot IRs could be reasonably explained by the hypothesis that a DSB event first occurred at IR
<sub>B </sub>
and led to the expansion of IRs to
<italic>trnH</italic>
, followed by a successive DSB event within IR
<sub>A </sub>
and lead to the expansion of IRs to
<italic>rps19 </italic>
or to
<italic>rpl22 </italic>
so far. This implies that the duplication of
<italic>trnH-rps19 </italic>
gene cluster was prior to the diversification of extant monocot lineages. The duplicated
<italic>trnH </italic>
genes in the IR
<sub>B </sub>
of most monocots and non-monocot angiosperms have distinct fates, which are likely regulated by different expression levels of
<italic>S10</italic>
<sub>
<italic>A </italic>
</sub>
and
<italic>S10</italic>
<sub>
<italic>B </italic>
</sub>
promoters. Further study is needed to unravel the evolutionary significance of IR expansion in more recently diverged monocots.</p>
</sec>
</div>
</front>
<back>
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