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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Acquisition of new protein domains by coronaviruses: analysis of overlapping genes coding for proteins N and 9b in SARS coronavirus</title><author><name sortKey="Shukla, Aditi" sort="Shukla, Aditi" uniqKey="Shukla A" first="Aditi" last="Shukla">Aditi Shukla</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="GRID">grid.4562.5</institution-id><institution-id institution-id-type="ISNI">0000000100572672</institution-id><institution>Institute of Biochemistry, Center for Structural and Cell Biology in Medicine,</institution><institution>University of Lübeck,</institution></institution-wrap>Ratzeburger Allee 160, 23538 Lübeck, Germany</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="GRID">grid.4562.5</institution-id><institution-id institution-id-type="ISNI">0000000100572672</institution-id><institution>Graduate School for Computing in Medicine & Life Sciences,</institution><institution>University of Lübeck,</institution></institution-wrap>Lübeck, Germany</nlm:aff></affiliation></author><author><name sortKey="Hilgenfeld, Rolf" sort="Hilgenfeld, Rolf" uniqKey="Hilgenfeld R" first="Rolf" last="Hilgenfeld">Rolf Hilgenfeld</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="GRID">grid.4562.5</institution-id><institution-id institution-id-type="ISNI">0000000100572672</institution-id><institution>Institute of Biochemistry, Center for Structural and Cell Biology in Medicine,</institution><institution>University of Lübeck,</institution></institution-wrap>Ratzeburger Allee 160, 23538 Lübeck, Germany</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3"><institution-wrap><institution-id institution-id-type="GRID">grid.4562.5</institution-id><institution-id institution-id-type="ISNI">0000000100572672</institution-id><institution>German Center for Infection Research (DZIF),</institution><institution>University of Lübeck,</institution></institution-wrap>Lübeck, Germany</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">25410051</idno><idno type="pmc">7089080</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089080</idno><idno type="RBID">PMC:7089080</idno><idno type="doi">10.1007/s11262-014-1139-8</idno><date when="2014">2014</date><idno type="wicri:Area/Pmc/Corpus">000502</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000502</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Acquisition of new protein domains by coronaviruses: analysis of overlapping genes coding for proteins N and 9b in SARS coronavirus</title><author><name sortKey="Shukla, Aditi" sort="Shukla, Aditi" uniqKey="Shukla A" first="Aditi" last="Shukla">Aditi Shukla</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="GRID">grid.4562.5</institution-id><institution-id institution-id-type="ISNI">0000000100572672</institution-id><institution>Institute of Biochemistry, Center for Structural and Cell Biology in Medicine,</institution><institution>University of Lübeck,</institution></institution-wrap>Ratzeburger Allee 160, 23538 Lübeck, Germany</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="GRID">grid.4562.5</institution-id><institution-id institution-id-type="ISNI">0000000100572672</institution-id><institution>Graduate School for Computing in Medicine & Life Sciences,</institution><institution>University of Lübeck,</institution></institution-wrap>Lübeck, Germany</nlm:aff></affiliation></author><author><name sortKey="Hilgenfeld, Rolf" sort="Hilgenfeld, Rolf" uniqKey="Hilgenfeld R" first="Rolf" last="Hilgenfeld">Rolf Hilgenfeld</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="GRID">grid.4562.5</institution-id><institution-id institution-id-type="ISNI">0000000100572672</institution-id><institution>Institute of Biochemistry, Center for Structural and Cell Biology in Medicine,</institution><institution>University of Lübeck,</institution></institution-wrap>Ratzeburger Allee 160, 23538 Lübeck, Germany</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3"><institution-wrap><institution-id institution-id-type="GRID">grid.4562.5</institution-id><institution-id institution-id-type="ISNI">0000000100572672</institution-id><institution>German Center for Infection Research (DZIF),</institution><institution>University of Lübeck,</institution></institution-wrap>Lübeck, Germany</nlm:aff></affiliation></author></analytic><series><title level="j">Virus Genes</title><idno type="ISSN">0920-8569</idno><idno type="eISSN">1572-994X</idno><imprint><date when="2014">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Acquisition of new proteins by viruses usually occurs through horizontal gene transfer or through gene duplication, but another, less common mechanism is the usage of completely or partially overlapping reading frames. A case of acquisition of a completely new protein through introduction of a start codon in an alternative reading frame is the protein encoded by open reading frame (orf) 9b of SARS coronavirus. This gene completely overlaps with the nucleocapsid (N) gene (orf9a). Our findings indicate that the orf9b gene features a discordant codon-usage pattern. We analyzed the evolution of orf9b in concert with orf9a using sequence data of betacoronavirus-lineage b and found that orf9b, which encodes the overprinting protein, evolved largely independent of the overprinted orf9a. We also examined the protein products of these genomic sequences for their structural flexibility and found that it is not necessary for a newly acquired, overlapping protein product to be intrinsically disordered, in contrast to earlier suggestions. Our findings contribute to characterizing sequence properties of newly acquired genes making use of overlapping reading frames.
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<front><journal-meta><journal-id journal-id-type="nlm-ta">Virus Genes</journal-id><journal-id journal-id-type="iso-abbrev">Virus Genes</journal-id><journal-title-group><journal-title>Virus Genes</journal-title></journal-title-group><issn pub-type="ppub">0920-8569</issn><issn pub-type="epub">1572-994X</issn><publisher><publisher-name>Springer US</publisher-name><publisher-loc>Boston</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">25410051</article-id><article-id pub-id-type="pmc">7089080</article-id><article-id pub-id-type="publisher-id">1139</article-id><article-id pub-id-type="doi">10.1007/s11262-014-1139-8</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Acquisition of new protein domains by coronaviruses: analysis of overlapping genes coding for proteins N and 9b in SARS coronavirus</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Shukla</surname><given-names>Aditi</given-names></name><xref ref-type="aff" rid="Aff1">1</xref><xref ref-type="aff" rid="Aff2">2</xref></contrib><contrib contrib-type="author" corresp="yes"><name><surname>Hilgenfeld</surname><given-names>Rolf</given-names></name><address><phone>+49-451-500-4060</phone><phone>+49-177-2412455</phone><email>hilgenfeld@biochem.uni-luebeck.de</email></address><xref ref-type="aff" rid="Aff1">1</xref><xref ref-type="aff" rid="Aff3">3</xref></contrib><aff id="Aff1"><label>1</label><institution-wrap><institution-id institution-id-type="GRID">grid.4562.5</institution-id><institution-id institution-id-type="ISNI">0000000100572672</institution-id><institution>Institute of Biochemistry, Center for Structural and Cell Biology in Medicine,</institution><institution>University of Lübeck,</institution></institution-wrap>Ratzeburger Allee 160, 23538 Lübeck, Germany</aff><aff id="Aff2"><label>2</label><institution-wrap><institution-id institution-id-type="GRID">grid.4562.5</institution-id><institution-id institution-id-type="ISNI">0000000100572672</institution-id><institution>Graduate School for Computing in Medicine & Life Sciences,</institution><institution>University of Lübeck,</institution></institution-wrap>Lübeck, Germany</aff><aff id="Aff3"><label>3</label><institution-wrap><institution-id institution-id-type="GRID">grid.4562.5</institution-id><institution-id institution-id-type="ISNI">0000000100572672</institution-id><institution>German Center for Infection Research (DZIF),</institution><institution>University of Lübeck,</institution></institution-wrap>Lübeck, Germany</aff></contrib-group><pub-date pub-type="epub"><day>20</day><month>11</month><year>2014</year></pub-date><pub-date pub-type="ppub"><year>2015</year></pub-date><volume>50</volume><issue>1</issue><fpage>29</fpage><lpage>38</lpage><history><date date-type="received"><day>17</day><month>7</month><year>2014</year></date><date date-type="accepted"><day>25</day><month>10</month><year>2014</year></date></history><permissions><copyright-statement>© Springer Science+Business Media New York 2014</copyright-statement><license><license-p>This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.</license-p></license></permissions><abstract id="Abs1"><p>Acquisition of new proteins by viruses usually occurs through horizontal gene transfer or through gene duplication, but another, less common mechanism is the usage of completely or partially overlapping reading frames. A case of acquisition of a completely new protein through introduction of a start codon in an alternative reading frame is the protein encoded by open reading frame (orf) 9b of SARS coronavirus. This gene completely overlaps with the nucleocapsid (N) gene (orf9a). Our findings indicate that the orf9b gene features a discordant codon-usage pattern. We analyzed the evolution of orf9b in concert with orf9a using sequence data of betacoronavirus-lineage b and found that orf9b, which encodes the overprinting protein, evolved largely independent of the overprinted orf9a. We also examined the protein products of these genomic sequences for their structural flexibility and found that it is not necessary for a newly acquired, overlapping protein product to be intrinsically disordered, in contrast to earlier suggestions. Our findings contribute to characterizing sequence properties of newly acquired genes making use of overlapping reading frames.
</p><sec><title>Electronic supplementary material</title><p>The online version of this article (doi:10.1007/s11262-014-1139-8) contains supplementary material, which is available to authorized users.</p></sec></abstract><kwd-group xml:lang="en"><title>Keywords</title><kwd>SARS coronavirus</kwd><kwd>Accessory proteins</kwd><kwd>Overlapping reading frames</kwd><kwd>Orf9b</kwd><kwd>Nucleocapsid</kwd><kwd>Evolution</kwd></kwd-group><custom-meta-group><custom-meta><meta-name>issue-copyright-statement</meta-name><meta-value>© Springer Science+Business Media New York 2015</meta-value></custom-meta></custom-meta-group></article-meta></front><body><sec id="Sec1" sec-type="introduction"><title>Introduction</title><p>A codon is composed of three nucleotides and therefore, three reading frames are, in principle, possible within the same gene. The correct reading frame is determined by the start codon, usually ATG or, in RNA genomes, AUG. Occasionally, the same stretch of genome codes for more than one protein in different reading frames; in this case, the protein products are called “overprinted” (or “ancestral”) and “overprinting” (or “novel”) [<xref ref-type="bibr" rid="CR1">1</xref>]. For simplicity, proteins encoded by overlapping genes are often called “overlapping proteins” or “transframe proteins” [<xref ref-type="bibr" rid="CR2">2</xref>], because during their translation, there occurs either a +1 or −1 shift in the reading frame [<xref ref-type="bibr" rid="CR3">3</xref>]. Overlapping reading frames have been discovered in many organisms, but they are most commonly found in viruses because of their comparatively small-size genomes [<xref ref-type="bibr" rid="CR3">3</xref>–<xref ref-type="bibr" rid="CR7">7</xref>]. It has been proposed that translation of overlapping reading frames in RNA viruses occurs via leaky ribosomal scanning [<xref ref-type="bibr" rid="CR8">8</xref>–<xref ref-type="bibr" rid="CR13">13</xref>], ribosomal frameshifting [<xref ref-type="bibr" rid="CR14">14</xref>–<xref ref-type="bibr" rid="CR17">17</xref>], or stop-codon readthrough [<xref ref-type="bibr" rid="CR18">18</xref>–<xref ref-type="bibr" rid="CR20">20</xref>]. Recently, a -2 programmed ribosomal frameshift has been observed in the synthesis of an overlapping protein in members of the family <italic>Arteriviridae</italic> [<xref ref-type="bibr" rid="CR21">21</xref>, <xref ref-type="bibr" rid="CR22">22</xref>].</p><p>In terms of evolution, overlapping genes are considered a mechanism for creating novel proteins [<xref ref-type="bibr" rid="CR1">1</xref>, <xref ref-type="bibr" rid="CR5">5</xref>]. However, any point mutation occurring in an overlapping gene region affects two (or more) protein products at the same time. Several studies have been performed to show the evolutionary aspects of overlapping gene sets in viruses [<xref ref-type="bibr" rid="CR4">4</xref>, <xref ref-type="bibr" rid="CR7">7</xref>, <xref ref-type="bibr" rid="CR23">23</xref>–<xref ref-type="bibr" rid="CR28">28</xref>]. Here, we report a case study on a set of overlapping proteins in severe acute respiratory syndrome coronavirus (SARS-CoV). SARS is characterized by acute pulmonary inflammation with a case/fatality rate of about 10 % [<xref ref-type="bibr" rid="CR29">29</xref>, <xref ref-type="bibr" rid="CR30">30</xref>]. SARS-CoV first emerged in 2002 in Guangdong province, China, and developed into a widespread epidemic in the spring of 2003 [<xref ref-type="bibr" rid="CR29">29</xref>]. It is believed that the virus originated from a bat reservoir [<xref ref-type="bibr" rid="CR31">31</xref>–<xref ref-type="bibr" rid="CR33">33</xref>]. Although the epidemic ended in July 2003, it is not unlikely for SARS-CoV or a similar virus to re-surface again. This view is supported by the recent emergence of a new human betacoronavirus of lineage c, Middle-East respiratory syndrome (MERS) CoV [<xref ref-type="bibr" rid="CR34">34</xref>–<xref ref-type="bibr" rid="CR37">37</xref>], which is transmitted to humans from dromedary camels [<xref ref-type="bibr" rid="CR38">38</xref>–<xref ref-type="bibr" rid="CR40">40</xref>] but may have a bat origin as well [<xref ref-type="bibr" rid="CR41">41</xref>–<xref ref-type="bibr" rid="CR43">43</xref>]. As of October 16, 2014, 877 laboratory-confirmed human MERS cases have been reported since September 2012, including at least 317 deaths [<xref ref-type="bibr" rid="CR44">44</xref>].</p><p>The 30-kb single-stranded SARS-CoV RNA genome codes for at least 28 proteins. In the 3′-proximal third, small open reading frames (orfs) coding for the so-called accessory proteins are interspersed among the genes coding for the structural proteins [<xref ref-type="bibr" rid="CR45">45</xref>, <xref ref-type="bibr" rid="CR46">46</xref>]. These include orf3a/b, orf6, orf7a/b, orf8a/b, orf9b, and possibly orf9c (Fig. <xref rid="Fig1" ref-type="fig">1</xref>) [<xref ref-type="bibr" rid="CR45">45</xref>–<xref ref-type="bibr" rid="CR49">49</xref>]. Accessory proteins of SARS-CoV are thought to be important players involved in viral pathogenicity [<xref ref-type="bibr" rid="CR47">47</xref>–<xref ref-type="bibr" rid="CR50">50</xref>]. However, reverse genetic studies have demonstrated that these proteins are not required for viral replication in cell culture or transgenic mice expressing human ACE2, the receptor for SARS-CoV [<xref ref-type="bibr" rid="CR51">51</xref>–<xref ref-type="bibr" rid="CR53">53</xref>]. Here we present the results of an investigation into the evolution and differential selection affecting the orf9b protein. This gene completely overlaps with the gene coding for the 422-amino-acid residue nucleocapsid (N) protein (Fig. <xref rid="Fig1" ref-type="fig">1</xref>). Recently, it has been proposed that leaky ribosomal scanning is responsible for the production of the overlapping orf9b protein [<xref ref-type="bibr" rid="CR54">54</xref>]. Orf9b codes for a small protein of 98 amino-acid residues, which is found in SARS-CoV-infected cells [<xref ref-type="bibr" rid="CR55">55</xref>]. Antibodies against this protein have been detected in the sera of SARS patients, demonstrating that the protein is produced during infection [<xref ref-type="bibr" rid="CR50">50</xref>, <xref ref-type="bibr" rid="CR56">56</xref>]. There has also been a report of yet another overlapping gene, orf9c, within the nucleocapsid gene, coding for a predicted protein of 70 amino-acid residues [<xref ref-type="bibr" rid="CR45">45</xref>, <xref ref-type="bibr" rid="CR46">46</xref>] (see Fig. <xref rid="Fig1" ref-type="fig">1</xref>). Until now, no evidence of orf9c expression has become available and since it is not well annotated, we will not include this gene in our analysis.<fig id="Fig1"><label>Fig. 1</label><caption><p><bold>a</bold> Schematic organization of the SARS-coronavirus genome, highlighting structural, and accessory genes. The overprinting accessory genes are indicated below their overprinted mates. <bold>b</bold> Overlapping N and orf9b genes of SARS-CoV with their start-stop coordinates within the genome (“end” coordinates include the stop codon)</p></caption><graphic xlink:href="11262_2014_1139_Fig1_HTML" id="MO1"></graphic></fig></p><p>In case of the overlapping nucleocapsid and orf9b genes of SARS-CoV, we are in the fortunate and rare situation that a large body of sequence data is available, as many isolates of the virus and its relatives from civets and bats were analyzed during and after the outbreak of 2003 [<xref ref-type="bibr" rid="CR57">57</xref>]. In addition, crystal structures have been determined for both the overlapping proteins [<xref ref-type="bibr" rid="CR58">58</xref>, <xref ref-type="bibr" rid="CR59">59</xref>], allowing conclusions that would not be possible in most cases of overlapping viral genes. In order to shed light onto the evolution of orf9b in concert with the nucleocapsid gene, we analyzed the codon-usage patterns of the two genes and the effects of the overlap on their mutation rates as well as on the three-dimensional structures of their protein products.</p></sec><sec id="Sec2" sec-type="materials|methods"><title>Methods</title><p>Seventy full-length genomic sequences including one reference sequence of SARS-CoV (isolate Tor2) were retrieved from the GenBank database (<ext-link ext-link-type="uri" xlink:href="http://www.ncbi.nlm.nih.gov/Genbank/index.html">http://www.ncbi.nlm.nih.gov/Genbank/index.html</ext-link>). Among these, 37 were from human SARS-CoV isolates, 15 from civet SARS-CoV, and 18 (including the newly discovered SL-CoV-WIV1 [<xref ref-type="bibr" rid="CR33">33</xref>]) from bat betacoronaviruses lineage b. Accession numbers are given in Table S1 (Online Resource 1). Unless explicitly stated otherwise, all these viruses are collectively called “SARS-CoV” in this work. These full-length genomic sequences were parsed and corresponding gene and amino-acid sequences were collected in a local database for further analysis.</p><sec id="Sec3"><title>Codon-usage analysis</title><p>Codon-usage analysis was done using the “sequence analysis program” within the Sequence Manipulation Suite [<xref ref-type="bibr" rid="CR60">60</xref>]. This program accepts one or more nucleotide sequence(s) and returns the number and frequency of each codon type. Relative Synonymous Codon Usage (RSCU) values were calculated using the frequencies of each codon type of a nucleotide sequence. The RSCU value for a codon i is calculated by: RSCU (i) = (observed i)/(expected i), where “observed i” is the observed frequency of codon i in a gene and “expected i” is the frequency expected assuming equal usage of synonymous codons for an amino acid in a gene.</p><p>The RSCU index is a measure to assess whether a sequence shows a preference for particular synonymous codons, i.e., codons that code for the same amino acid. The comparison was done at the level of codon usage between overlapping and non-overlapping coding regions. The RSCU values obtained from the overlapping orf9a/9b genes were then compared with those of the non-overlapping regions of the same viral genome by means of the Pearson correlation coefficient “r” [<xref ref-type="bibr" rid="CR61">61</xref>]. Values of r range from −1 to +1, reflecting a completely different and identical degree in the usage of synonymous codons, respectively. Discordant usage suggests the gene to be relatively new [<xref ref-type="bibr" rid="CR62">62</xref>, <xref ref-type="bibr" rid="CR63">63</xref>].</p></sec><sec id="Sec4"><title>Mutation rate analysis</title><p>Mutation rate analysis was performed by first aligning both the nucleotide and protein sequences using ClustalX version 2.1 [<xref ref-type="bibr" rid="CR64">64</xref>]. Redundant sequences (from multiple human patients) were manually removed. DnaSP 5.10 [<xref ref-type="bibr" rid="CR65">65</xref>] was used to calculate the number of synonymous and nonsynonymous substitutions at the overlapping gene regions of the N gene and the orf9b gene.</p></sec><sec id="Sec5"><title>Entropy-plotting of alignments</title><p>Entropy-plotting of alignments was done to determine the variations occurring in the overprinted N protein and the overprinting orf9b protein. Variation in the three sets of nucleotide sites of a codon and the variation in the corresponding amino-acid residues in the overlapping proteins were studied by plotting the entropy (variability) of the aligned overlapping nucleotide and protein sequences, as implemented in the BioEdit software v7.0.0. [<xref ref-type="bibr" rid="CR66">66</xref>]. The entropy is defined as a measure of uncertainty at each position in a set of aligned nucleotide or protein sequences [<xref ref-type="bibr" rid="CR66">66</xref>]. The cumulative entropy is the sum of all the entropy values calculated at each position in a sequence. For calculating the entropy, sequences are treated as a matrix of characters and the maximum number of different characters found in a column (column of aligned sets of nucleotide or protein sequences) defines the maximum total uncertainty or the “entropy” [<xref ref-type="bibr" rid="CR66">66</xref>]. The entropy H is calculated by H(l) = −∑f(b,l)ln(f(b,l)), where H(l) is the uncertainty (entropy) at position l, b represents a residue (out of the allowed choices for the sequence under investigation), and f(b,l) is the frequency at which residue b is found at position l. We determined the frequency of substitutions at each codon site in the overlapping region of the nucleocapsid/orf9b gene to find out the evolutionary strategy followed by this set of overlapping genes in SARS-CoV. There are 98 codons in the overlapping region and we studied the variation of nucleotides (294 codon positions) and their corresponding amino acids in the overlapping nucleocapsid and orf9b gene region of 70 SARS-CoV genomes.</p></sec><sec id="Sec6"><title>Inspection of crystal structures and prediction of disorder</title><p>Inspection and presentation of crystal structures of the N-terminal domain (NTD) of the N protein (orf9a) [<xref ref-type="bibr" rid="CR58">58</xref>] and the orf9b protein of SARS-CoV [<xref ref-type="bibr" rid="CR59">59</xref>] were performed using the program Pymol (Schrödinger), in order to assess possible consequences of the overlapping genes for the three-dimensional structures of the protein products. Disorder prediction was also carried out for these overlapping proteins because crystallographic information is not available for the N-terminal 46 residues of the overprinted N protein. For this purpose, the DisProt VSL2 intrinsic-disorder prediction program was used [<xref ref-type="bibr" rid="CR67">67</xref>].</p></sec></sec><sec id="Sec7" sec-type="results"><title>Results</title><sec id="Sec8"><title>Codon usage in the overlapping gene set</title><p>The first step of our analysis was to establish a relationship between the codon usage in overlapping and non-overlapping genes in the betacoronavirus SARS-CoV. Two-thirds of the SARS-CoV genome comprise orf1ab, which encodes the viral polyproteins pp1a and pp1ab. The 3′-proximal third comprises orfs encoding the structural proteins, i.e., spike (S), envelope (E), membrane (M), and nucleocapsid (N), as well as several accessory proteins as described previously [<xref ref-type="bibr" rid="CR45">45</xref>, <xref ref-type="bibr" rid="CR46">46</xref>]. The non-overlapping regions of the genome (Fig. <xref rid="Fig1" ref-type="fig">1</xref>) were combined into a single unit including the orf1a, orf1b, spike, envelope, membrane, and orf6 genes. On the other hand, the genes under study here, full-length nucleocapsid and the overlapping orf9b, were considered distinct sets of data. The remaining accessory proteins were not included in this comparison because they contain partially overlapping regions.</p><p>The subsequent correlation analysis (Table <xref rid="Tab1" ref-type="table">1</xref>) shows that the internal overlapping gene (orf9b) exhibits a choice of synonymous codons highly different from that occurring in the non-overlapping gene set of SARS-CoV, exhibiting an <italic>r</italic> value of −0.01. For example, of the eight proline residues in the orf9b protein, five (63 %) are coded by CCC, whereas in the non-overlapping gene set, less than 9 % of proline residues use this codon. A much higher degree of concordant relationship is seen between the overprinted N gene of SARS-CoV and the non-overlapping gene set (<italic>r</italic> value of 0.62).<table-wrap id="Tab1"><label>Table 1</label><caption><p>Correlation between the codon-usage patterns of the overlapping N and its overprinting internal genes of SARS-CoV, as well as of other members of the genus <italic>Betacoronavirus,</italic> i.e., BCoV, MHV, and MERS-CoV, each with the non-overlapping coding regions in their genome</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="left"><italic>Betacoronavirus</italic></th><th align="left">Proteins</th><th align="left">Number of amino-acid residues</th><th align="left">Correlation coefficient (r)</th></tr></thead><tbody><tr><td align="left" rowspan="2">SARS-CoV</td><td align="left">Nucleocapsid</td><td align="left">422</td><td char="." align="char">0.62</td></tr><tr><td align="left">Orf9b</td><td align="left">98</td><td char="." align="char">−0.01</td></tr><tr><td align="left" rowspan="2">BCoV</td><td align="left">Nucleocapsid</td><td align="left">448</td><td char="." align="char">0.67</td></tr><tr><td align="left">internal protein</td><td align="left">207</td><td char="." align="char">−0.11</td></tr><tr><td align="left" rowspan="2">MHV</td><td align="left">Nucleocapsid</td><td align="left">455</td><td char="." align="char">0.66</td></tr><tr><td align="left">internal protein</td><td align="left">136</td><td char="." align="char">0.00</td></tr><tr><td align="left" rowspan="2">MERS-CoV</td><td align="left">Nucleocapsid</td><td align="left">411</td><td char="." align="char">0.58</td></tr><tr><td align="left">hypothetical internal protein</td><td align="left">112</td><td char="." align="char">−0.13</td></tr></tbody></table></table-wrap></p><p>Codon-usage analysis for other betacoronaviruses containing a hypothetical overlapping “internal” gene within their nucleocapsid gene was also carried out for comparison. The nucleocapsid genes of Bovine Coronavirus (BCoV, NCBI accession number NC_003045), Mouse Hepatitis Virus (MHV, AC_000192), and Middle-East Respiratory Syndrome coronavirus (MERS-CoV, NC_019843) display a similar positive correlation when compared to the rest of the genome, with <italic>r</italic> values of 0.67, 0.66, and 0.57, respectively, whereas their corresponding “internal” genes have <italic>r</italic> values of −0.11, 0.00, and −0.13, respectively (Table <xref rid="Tab1" ref-type="table">1</xref>).</p></sec><sec id="Sec100"><title>Effect of the overlap on the mutation rate in the N and orf9b genes and evolutionary strategy adopted by this overlapping gene set</title><p>The ratio ω of nonsynonymous (K<sub>a</sub>) to synonymous (K<sub>s</sub>) nucleotide substitution rates is an indicator of selective pressure on genes. A ratio significantly greater than 1 indicates positive selective pressure. A ratio around 1 indicates either neutral evolution at the protein level or an averaging of sites under positive and negative selective pressure. A ratio less than 1 indicates pressure to conserve protein sequence, i.e., “purifying selection” [<xref ref-type="bibr" rid="CR68">68</xref>].</p><p>The overlapping gene regions of nucleocapsid and orf9b show differences in the evolutionary rates. The overprinted region of the nucleocapsid gene in SARS-CoV has a K<sub>a</sub>/K<sub>s</sub> ratio of 0.56 (the K<sub>a</sub>/K<sub>s</sub> ratio is 0.62 for the non-overlapping part of the N gene). On the other hand, the orf9b gene has a K<sub>a</sub>/K<sub>s</sub> ratio greater than 1 (Table <xref rid="Tab2" ref-type="table">2</xref>), which means that the orf9b protein is subject to positive selection pressure and is evolving at a faster rate, compared to the overprinted N gene. Remarkably, due to the difference in frame phase (see below), the same stretch of genome has thus different evolutionary rates when coding for each of the two different proteins. This observation prompted us to analyze the nucleotide variations at each of the three nucleotide positions of the codons.<table-wrap id="Tab2"><label>Table 2</label><caption><p>Synonymous and nonsynonymous substitutions in overlapping and non-overlapping regions of the SARS-CoV nucleocapsid gene and in the orf9b gene</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="left">Gene regions of:</th><th align="left">K<sub>a</sub></th><th align="left">K<sub>s</sub></th><th align="left">K<sub>a</sub>/K<sub>s</sub> = ω</th></tr></thead><tbody><tr><td align="left">Nucleocapsid (overlapping part)</td><td char="." align="char">0.41</td><td char="." align="char">0.73</td><td char="." align="char">0.56</td></tr><tr><td align="left">Nucleocapsid (non-overlapping part)</td><td char="." align="char">0.37</td><td char="." align="char">0.59</td><td char="." align="char">0.62</td></tr><tr><td align="left">Orf9b</td><td char="." align="char">0.53</td><td char="." align="char">0.43</td><td char="." align="char">1.23</td></tr></tbody></table></table-wrap></p><p>Upon a point mutation, the position at which nucleotide substitution occurs within a codon reflects whether the substitution would be synonymous or not. When there is a nucleotide substitution at the first codon position, it causes an amino-acid change in 60 out of 64 cases. The four exceptions occur because of the partial degeneration of codons at this position. At this codon site, there are four possibilities, which would result in a synonymous substitution: two each in codons for leucine (UUA vs. CUA, UUG vs. CUG) and arginine (AGA vs. CGA, AGG vs. CGG). When there is a nucleotide substitution at the second codon position, it results in an amino-acid change in 63 out of 64 cases. At this codon site, the only substitution that is synonymous occurs in the stop codons UAA versus UGA. Lastly, a nucleotide substitution occurring at the third codon position causes a change in amino acid in only 16 out of 64 cases because of codon degeneracy at the third nucleotide position [<xref ref-type="bibr" rid="CR25">25</xref>, <xref ref-type="bibr" rid="CR62">62</xref>, <xref ref-type="bibr" rid="CR63">63</xref>].</p><p>As a result of leaky ribosomal scanning [<xref ref-type="bibr" rid="CR54">54</xref>], translation of orf9b begins at the 10th nucleotide position of the N gene (Fig. <xref rid="Fig2" ref-type="fig">2</xref>a), resulting in a +1 difference in reading frame between orf9b ((+1)-phase frame) and the N gene (0-phase frame). Thus, the first nucleotide position of an N codon corresponds to the third nucleotide position of an orf9b codon (N1/9b3), the second position in an N codon corresponds to the first nucleotide position in an orf9b codon (N2/9b1), and the third position in an N codon corresponds to the second nucleotide position in an orf9b codon (N3/9b2) (Fig. <xref rid="Fig2" ref-type="fig">2</xref>a). Hence, as described above, a nucleotide substitution in the first position of a nucleocapsid codon (N1/9b3) is likely to cause an amino-acid change in N, but not in orf9b, whereas substitutions in the third position of an N codon (N3/9b2) are probably nonsynonymous in orf9b, but synonymous in N.<fig id="Fig2"><label>Fig. 2</label><caption><p><bold>a</bold><italic>Top</italic>: The 5′ ends of the SARS-CoV N and orf9b genes. At nucleotide no. 10 of the N gene, translation of the overlapping orf9b gene begins, resulting in a phase difference of +1 for this gene relative to the N gene. <italic>Bottom</italic>: Codon-site substitutions in the two genes. Three types of substitution have to be distinguished: N2/9b1, N3/9b2, N1/9b3. <bold>b</bold> Variation of three sets of nucleotides (in <italic>magenta</italic>): N1/9b3, N2/9b1, and N3/9b2, in relation to the amino-acid variations (in <italic>blue</italic>) in the overlapping nucleocapsid and orf9b proteins. The <italic>x</italic>-axis represents the codon sites in case of graphs <xref rid="Fig1" ref-type="fig">1</xref>, 3, and 5, i.e., nucleotide variations, whereas in case of graphs 2 and 4, the <italic>x</italic>-axis represents the amino-acid residue number. Note that the N protein overlaps with orf9b between its residues 4 and 101; however, in graph 2, which represents the amino-acid variations in the N protein, the <italic>x</italic>-axis is calibrated from 1 to 98 in order to facilitate the comparison with orf9b. The <italic>y</italic>-axis represents entropy. The <italic>green dot</italic> indicates the one case of synonymous N1/9b3 substitution that does not lead to an amino-acid exchange in the N protein because of the partial degeneration of the first nucleotide position in a codon (AGA and CGA both code for Arg). The <italic>red dot</italic> indicates a case of a two-nucleotide difference as a result of an N1/9b3 and an N2/9b1 substitution that leads to an amino-acid exchange in the N protein. All bat betacoronaviruses of lineage b (with the exception of SL-CoV WIV1 [<xref ref-type="bibr" rid="CR33">33</xref>]) have Lys at this position, whereas all civet and human SARS-CoV isolates as well as bat SL-CoV WIV1 have Pro (see text)</p></caption><graphic xlink:href="11262_2014_1139_Fig2_HTML" id="MO2"></graphic></fig></p><p>The nucleotide variation at the 98 N1/9b3, N2/9b1, and N3/9b2 positions (see Fig. <xref rid="Fig2" ref-type="fig">2</xref>a) of the overlapping N/orf9b gene region for all 70 sequences is shown in Fig. <xref rid="Fig2" ref-type="fig">2</xref>b. We find that the value of cumulative mutational frequency (∑(H); see “<xref rid="Sec2" ref-type="sec">Methods</xref>” section) of the overlapping region of the nucleocapsid protein is 4.7 and that of the orf9b protein is 15.3. This difference in the frequency of mutation was somewhat expected, based on the different ω values for the two genes (see Table <xref rid="Tab2" ref-type="table">2</xref>). Moving on to the nucleotide level, we obtain cumulative entropy values of 3.16, 3.49, and 5.44 for the N1/9b3, N2/9b1, and N3/9b2 codon positions, respectively. The graphs are calibrated in the range of 0–1 for accurate comparison of the results of protein sequences with nucleotide sequences (Fig. <xref rid="Fig2" ref-type="fig">2</xref>b).</p><p>The higher rate of amino-acid variation in the orf9b protein is largely determined by nucleotide substitutions at the N3/9b2 sites. All the N3/9b2 nucleotide variations translate to amino-acid changes in the orf9b protein but are silent in the nucleocapsid protein. Amino-acid variations in the nucleocapsid protein are determined by substitutions of N1/9b3 nucleotides. In one instance, an N1/9b3 nucleotide variation results in a synonymous mutation in the nucleocapsid protein (Fig. <xref rid="Fig2" ref-type="fig">2</xref>b, green dot). The amino acid at this position is arginine and this phenomenon occurs due to partial degeneration of the first nucleotide position as explained above.</p><p>There are a few N2/9b1 mutations that impose amino-acid variations in both the proteins. An interesting variation, corresponding to a concomitant N1/9b3 and N2/9b1 exchange, results in an amino-acid difference at position 81 of the nucleocapsid protein, within its well-ordered and overprinted part. All known genomic sequences of bat betacoronaviruses of lineage b feature the AAA triplet (coding for Lys) here, whereas all isolates of civet and human SARS-CoV have CCA (coding for Pro). The exception among the bat beta-CoVs of lineage b is the newly discovered SL-CoV WIV1, which is proposed to be the likely originator of SARS-CoV [<xref ref-type="bibr" rid="CR33">33</xref>]; the N gene of this virus also has CCA coding for Pro at this position. Thus, there is a two-nucleotide difference between the codons in the bat CoVs (except SL-CoV WIV1) on the one hand and human or civet SARS-CoV on the other (see red dot in Fig. 4). In the orf9b protein, the corresponding codon (shifted by +1 in frame) is AAG (coding for Lys) in the bat betacoronaviruses of lineage b, and CAG (coding for Gln) in the civet and human SARS-CoV sequences as well as in SL-CoV WIV1 [<xref ref-type="bibr" rid="CR33">33</xref>]. Thus, only the N2/9b1 variation results in an amino-acid change in the orf9b protein and the N1/9b3 nucleotide variation is silent.</p></sec><sec id="Sec9"><title>Effect of overlaps on the three-dimensional structures of the protein products</title><p>Crystal structures are available for both the N-terminal RNA-binding domain (NTD) of the SARS-CoV nucleocapsid protein [<xref ref-type="bibr" rid="CR58">58</xref>] (PDB code: 2OFZ) and the orf9b protein [<xref ref-type="bibr" rid="CR59">59</xref>] (PDB code: 2CME). The N-terminal 46 residues of the NTD have been excluded from the fragment that was crystallized, as they are believed to be disordered on the basis of secondary structure prediction, limited proteolysis experiments, and sequence conservation. The well-ordered global NTD (residues 47–175) comprises an antiparallel β-sheet core and a β-hairpin protruding from it (Fig. <xref rid="Fig3" ref-type="fig">3</xref>a). The orf9b protein forms a two-fold symmetric dimer comprising two adjacent β-sheets (Fig. <xref rid="Fig3" ref-type="fig">3</xref>a). In the central hydrohobic cavity between the monomers, electron density for a lipid molecule was detected [<xref ref-type="bibr" rid="CR59">59</xref>]. The global part of the nucleocapsid NTD exhibits reduced flexibility, as evident from the atomic temperature factors (B-factors) for the polypeptide. The average B-factor for the NTD (residues 47–175) is 11.2 Å<sup>2</sup> [<xref ref-type="bibr" rid="CR58">58</xref>]. In contrast, the orf9b protein appears to be much more flexible; its average B-factor is 100.8 Å<sup>2</sup> [<xref ref-type="bibr" rid="CR59">59</xref>]. Even though a number of factors contribute to the B value, in particular the degree of disorder of the crystal, rigid-body movements of the molecules, experimental errors, etc., it is evident from this huge difference between the B values for the two structures that the orf9b polypeptide chain is very flexible. In line with this, the segments between residues 1–8 and 26–37 in the orf9b protein are not visible in the electron-density maps. This result supports the notion that overprinting proteins tend to show higher flexibility and disorder [<xref ref-type="bibr" rid="CR1">1</xref>]. In contrast, all residues are well defined by electron density in the NTD crystal structure of the overlapping N protein. However, it should also be mentioned that probably, many residues are disordered or highly flexible among the N-terminal 46 residues of the NTD, which have not been included in the construct employed in crystal structure determination but belong to the overlapping region (with the exception of the first three residues) as seen in a prediction using the program DisProt VSL2B [<xref ref-type="bibr" rid="CR67">67</xref>] (Fig. <xref rid="Fig3" ref-type="fig">3</xref>b).<fig id="Fig3"><label>Fig. 3</label><caption><p><bold>a</bold> Structures of the SARS-CoV proteins investigated in this study, colored according to the B-factor (color scheme used is VIBGYOR, where <italic>Violet</italic> depicts the minimum and <italic>red</italic> depicts the maximum value of B-factor) averaged for each amino-acid residue; (<italic>left</italic>) NTD of nucleocapsid protein (overall average B-factor 11.19 Å<sup>2;</sup> PDB code 2OFZ [<xref ref-type="bibr" rid="CR58">58</xref>] ); (<italic>right</italic>) Dimer of the orf9b protein (overall average B-factor 100.8 Å<sup>2</sup>, PDB code 2CME [<xref ref-type="bibr" rid="CR59">59</xref>] ). <bold>b</bold> Disorder prediction result for the NTD of the SARS-CoV nucleocapsid protein and its overprinting counterpart, the orf9b protein, calculated using the program DisProt VSL2B [<xref ref-type="bibr" rid="CR67">67</xref>]. The degree of order–disorder lies within the range of 0 (well ordered) to 1 (highly disordered)</p></caption><graphic xlink:href="11262_2014_1139_Fig3_HTML" id="MO3"></graphic></fig></p><p>We also made an attempt to locate the amino-acid variations, which we identified in the 70 sequences of our data set, in the three-dimensional structures of the nucleocapsid [<xref ref-type="bibr" rid="CR58">58</xref>] and orf9b [<xref ref-type="bibr" rid="CR59">59</xref>] proteins. In the overprinted part of the nucleocapsid NTD, the majority of mutations occur in the unstructured N-terminal region (residues 1–46). Residue 81, which is Lys in all sequenced bat betacoronaviruses of lineage b (except SL-CoV WIV1) but Pro in all civet and human SARS-CoV strains, is located at position 2 of a surface-exposed type-III β-turn of the sequence Gly-Pro-Asp-Asp. In the orf9b structure, the corresponding residue (Gln in SARS-CoV and SL-CoV WIV1) is not defined by electron density and hence part of a presumably disordered region. In fact, in the orf9b protein, all mutations occur in the regions that have been reported to be disordered [<xref ref-type="bibr" rid="CR59">59</xref>]. Thus, the general observation that mutations are more commonly localized in regions of no regular secondary structure (such as loops etc.) rather than in α-helices or β-strands, remains valid for this overprinting protein.</p></sec></sec><sec id="Sec10" sec-type="discussion"><title>Discussion</title><p>Previous work has suggested codon usage as a measure to determine the relative age of a gene. A discordant relationship in the codon usage of a particular gene, when compared with the rest of the genes, suggests that the gene has evolved recently [<xref ref-type="bibr" rid="CR1">1</xref>, <xref ref-type="bibr" rid="CR25">25</xref>, <xref ref-type="bibr" rid="CR28">28</xref>, <xref ref-type="bibr" rid="CR62">62</xref>, <xref ref-type="bibr" rid="CR63">63</xref>]. It has been shown that this phenomenon can be applied to identify overprinting viral proteins [<xref ref-type="bibr" rid="CR63">63</xref>]. Research on overlapping protein products in RNA viruses has suggested that proteins of the overprinting genes have a tendency to be structurally disordered [<xref ref-type="bibr" rid="CR1">1</xref>]. Taking into account these observations, we have analyzed the sequence and structural properties of the overlapping proteins nucleocapsid and orf9b in SARS-CoV, in the hope of gaining insight into the creation of novel proteins in RNA viruses. Studies revealing differential selective pressure during the evolution of overlapping viral genes [<xref ref-type="bibr" rid="CR23">23</xref>–<xref ref-type="bibr" rid="CR27">27</xref>, <xref ref-type="bibr" rid="CR62">62</xref>] led us to probe the selection pressure acting on the overlapping N and orf9b genes.</p><p>Codon-usage analysis shows that the overprinting orf9b has a discordant codon-usage pattern whereas the overprinted region of the nucleocapsid gene has a codon-usage pattern similar to the non-overlapping regions of the SARS-CoV genome. The discordant codon-usage pattern suggests a relatively more recent acquisition of the orf9b gene [<xref ref-type="bibr" rid="CR62">62</xref>, <xref ref-type="bibr" rid="CR63">63</xref>]. Moreover, no sequence similarity exists between the orf9b protein and any other known proteins [<xref ref-type="bibr" rid="CR45">45</xref>, <xref ref-type="bibr" rid="CR46">46</xref>]. Among other coronaviruses, internal open reading frames within the nucleocapsid gene have been reported for members of <italic>Betacoronavirus</italic> lineage a, for example Bovine Coronavirus, Mouse Hepatitis Virus, and human coronaviruses HKU1 and OC43 [<xref ref-type="bibr" rid="CR69">69</xref>–<xref ref-type="bibr" rid="CR71">71</xref>]. Moreover, they can also be found in members of <italic>Betacoronavirus</italic> lineage c, i.e., MERS Coronavirus [<xref ref-type="bibr" rid="CR36">36</xref>] as well as bat coronaviruses HKU4 and HKU5. However, there is little in common between the orf9b gene of SARS-CoV and these so-called “internal” genes [<xref ref-type="bibr" rid="CR49">49</xref>]. Hence, we can conclude that orf9b is a novel gene.</p><p>A previous study performed on the translation mechanism employed in orf9b expression describes the presence of a sub-optimal Kozak sequence for the N gene [<xref ref-type="bibr" rid="CR54">54</xref>]. In contrast, the start codon of the orf9b gene resides within an optimal Kozak sequence, but the properties of the second initiation site in leaky ribosomal scanning do not influence the decision of the ribosome to stop at or bypass the first AUG [<xref ref-type="bibr" rid="CR9">9</xref>]. Xu et al. [<xref ref-type="bibr" rid="CR54">54</xref>] showed that the expression level of the orf9b gene is relatively weaker when compared to that of the N gene. This is probably caused by only a fraction of ribosomes bypassing the first AUG, but may also be influenced by the fact that the codon usage of orf9b is different from that of the rest of the SARS-CoV genes (Table <xref rid="Tab1" ref-type="table">1</xref>). In addition, although orf9b production appears to depend on leaky ribosomal scanning, we cannot exclude that the expression of this gene is modulated by other SARS-CoV proteins, as described very recently for members of the family <italic>Arteriviridae</italic> [<xref ref-type="bibr" rid="CR21">21</xref>, <xref ref-type="bibr" rid="CR22">22</xref>]. The orf9b protein has been shown to interact with several other SARS-CoV proteins, for example Nsp5, Nsp14, and the orf6 protein [<xref ref-type="bibr" rid="CR52">52</xref>, <xref ref-type="bibr" rid="CR72">72</xref>]. It remains to be investigated whether any of these can transactivate or suppress the expression of the alternating gene, orf9b.</p><p>The evolution of overlapping, frame-shifted genes is subject to extra constraints. A slower rate of evolution has been demonstrated in overlapping genes in a number of viruses [<xref ref-type="bibr" rid="CR7">7</xref>, <xref ref-type="bibr" rid="CR23">23</xref>–<xref ref-type="bibr" rid="CR26">26</xref>]. There is an imposing constraint in evolution of overlapping genes due to the fact that a favorable or even neutral substitution in one reading frame could prove harmful for the other reading frame. Therefore, even a synonymous, favorable, or neutral nucleotide substitution in one reading frame might be discarded, as it could be deleterious in the other reading frame. As a result, positive selection of overlapping genes in general is severely restricted [<xref ref-type="bibr" rid="CR7">7</xref>, <xref ref-type="bibr" rid="CR23">23</xref>–<xref ref-type="bibr" rid="CR26">26</xref>]. However, here we demonstrated that the overlapping region of the N gene is rather evolutionary conserved when compared to the orf9b gene. Orf9b features a higher evolutionary rate that is attained mainly via N3/9b2 substitutions. This mechanism of independent evolution is similar to the mechanism of “independent adaptive selection” recently described for the gene encoding the Hepatitis B Virus (HBV) surface protein which completely overlaps with the polymerase gene [<xref ref-type="bibr" rid="CR27">27</xref>].</p><p>A structural comparison of the overlapping NTD of the nucleocapsid protein with the orf9b protein indicates the latter to be more flexible (Fig. <xref rid="Fig3" ref-type="fig">3</xref>). However, 50 % of the overlapping orf9b protein corresponds to the structurally undetermined segment 1–46 of the NTD of the nucleocapsid protein. This region is predicted to be intrinsically disordered (see Fig. <xref rid="Fig3" ref-type="fig">3</xref>b) [<xref ref-type="bibr" rid="CR73">73</xref>]. Consequently, the overprinting orf9b protein is more ordered in its N-terminal half than the overprinted N-terminal segment 1–46 of the nucleocapsid NTD. More studies on overlapping viral proteins with known three-dimensional structures would be necessary to refine our understanding of the evolutionary and structural constraints caused by this phenomenon.</p><p>Currently, the function of the orf9b protein is unknown, although its crystal structure [<xref ref-type="bibr" rid="CR59">59</xref>] suggests that it may bind lipids. Since the protein evolved with a high rate and independently of the overprinted nucleocapsid protein, it may have the potential to acquire new functions in a relatively short time. The analysis presented here may form a basis to follow the future evolution of orf9b and a starting point for investigating the so-called “internal genes” overlapping with the nucleocapsid gene in other coronaviruses, including MERS-CoV. Beyond its importance for understanding coronavirus evolution, our study may have implications for the analysis of overlapping reading frames in other viruses as well.</p></sec><sec sec-type="supplementary-material"><title>Electronic supplementary material</title><sec id="Sec11"><p>Below is the link to the electronic supplementary material.
<supplementary-material content-type="local-data" id="MOESM1"><media xlink:href="11262_2014_1139_MOESM1_ESM.docx"><caption><p>Supplementary material 1 (DOCX 78 kb)</p></caption></media></supplementary-material></p></sec></sec></body><back><ack><p>We thank Dr. Zhengli Shi of the Wuhan Institute of Virology, Chinese Academy of Sciences, for sharing the sequence of the SL-CoV WIV1 nucleocapsid gene with us prior to publication. 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