Identification of Novel Subgenomic RNAs and Noncanonical Transcription Initiation Signals of Severe Acute Respiratory Syndrome Coronavirus
Identifieur interne : 000E90 ( Ncbi/Checkpoint ); précédent : 000E89; suivant : 000E91Identification of Novel Subgenomic RNAs and Noncanonical Transcription Initiation Signals of Severe Acute Respiratory Syndrome Coronavirus
Auteurs : Snawar Hussain [République populaire de Chine] ; Ji'An Pan [République populaire de Chine] ; Yu Chen ; Yalin Yang [République populaire de Chine] ; Jing Xu [République populaire de Chine] ; Yu Peng ; Ying Wu [République populaire de Chine] ; Zhaoyang Li [République populaire de Chine] ; Ying Zhu [République populaire de Chine] ; Po Tien [République populaire de Chine] ; Deyin Guo [République populaire de Chine]Source :
- Journal of Virology [ 0022-538X ] ; 2005.
Descripteurs français
- KwdFr :
- ARN messager (génétique), ARN viral (biosynthèse), ARN viral (génétique), Animaux, Cadres ouverts de lecture, Cellules Vero, Cricetinae, Données de séquences moléculaires, Génome viral, Matrices (génétique), Site d'initiation de la transcription, Séquence nucléotidique, Transcription génétique, Virus du SRAS (génétique).
- MESH :
English descriptors
- KwdEn :
- Animals, Base Sequence, Chlorocebus aethiops, Cricetinae, Genome, Viral, Molecular Sequence Data, Open Reading Frames, RNA, Messenger (genetics), RNA, Viral (biosynthesis), RNA, Viral (genetics), SARS Virus (genetics), Templates, Genetic, Transcription Initiation Site, Transcription, Genetic, Vero Cells.
- MESH :
- chemical , biosynthesis : RNA, Viral.
- chemical , genetics : RNA, Messenger, RNA, Viral.
- genetics : SARS Virus.
- Animals, Base Sequence, Chlorocebus aethiops, Cricetinae, Genome, Viral, Molecular Sequence Data, Open Reading Frames, Templates, Genetic, Transcription Initiation Site, Transcription, Genetic, Vero Cells.
Abstract
The expression of the genomic information of severe acute respiratory syndrome coronavirus (SARS CoV) involves synthesis of a nested set of subgenomic RNAs (sgRNAs) by discontinuous transcription. In SARS CoV-infected cells, 10 sgRNAs, including 2 novel ones, were identified, which were predicted to be functional in the expression of 12 open reading frames located in the 3′ one-third of the genome. Surprisingly, one new sgRNA could lead to production of a truncated spike protein. Sequence analysis of the leader-body fusion sites of each sgRNA showed that the junction sequences and the corresponding transcription-regulatory sequence (TRS) are unique for each species of sgRNA and are consistent after virus passages. For the two novel sgRNAs, each used a variant of the TRS that has one nucleotide mismatch in the conserved hexanucleotide core (ACGAAC) in the TRS. Coexistence of both plus and minus strands of SARS CoV sgRNAs and evidence for derivation of the sgRNA core sequence from the body core sequence favor the model of discontinuous transcription during minus-strand synthesis. Moreover, one rare species of sgRNA has the junction sequence AAA, indicating that its transcription could result from a noncanonical transcription signal. Taken together, these results provide more insight into the molecular mechanisms of genome expression and subgenomic transcription of SARS CoV.
Url:
DOI: 10.1128/JVI.79.9.5288-5295.2005
PubMed: 15827143
PubMed Central: 1082772
Affiliations:
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PMC:1082772Le document en format XML
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<term>RNA, Messenger (genetics)</term>
<term>RNA, Viral (biosynthesis)</term>
<term>RNA, Viral (genetics)</term>
<term>SARS Virus (genetics)</term>
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<front><div type="abstract" xml:lang="en"><p>The expression of the genomic information of severe acute respiratory syndrome coronavirus (SARS CoV) involves synthesis of a nested set of subgenomic RNAs (sgRNAs) by discontinuous transcription. In SARS CoV-infected cells, 10 sgRNAs, including 2 novel ones, were identified, which were predicted to be functional in the expression of 12 open reading frames located in the 3′ one-third of the genome. Surprisingly, one new sgRNA could lead to production of a truncated spike protein. Sequence analysis of the leader-body fusion sites of each sgRNA showed that the junction sequences and the corresponding transcription-regulatory sequence (TRS) are unique for each species of sgRNA and are consistent after virus passages. For the two novel sgRNAs, each used a variant of the TRS that has one nucleotide mismatch in the conserved hexanucleotide core (ACGAAC) in the TRS. Coexistence of both plus and minus strands of SARS CoV sgRNAs and evidence for derivation of the sgRNA core sequence from the body core sequence favor the model of discontinuous transcription during minus-strand synthesis. Moreover, one rare species of sgRNA has the junction sequence AAA, indicating that its transcription could result from a noncanonical transcription signal. Taken together, these results provide more insight into the molecular mechanisms of genome expression and subgenomic transcription of SARS CoV.</p>
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<name sortKey="Pan, Ji An" sort="Pan, Ji An" uniqKey="Pan J" first="Ji'An" last="Pan">Ji'An Pan</name>
<name sortKey="Tien, Po" sort="Tien, Po" uniqKey="Tien P" first="Po" last="Tien">Po Tien</name>
<name sortKey="Wu, Ying" sort="Wu, Ying" uniqKey="Wu Y" first="Ying" last="Wu">Ying Wu</name>
<name sortKey="Xu, Jing" sort="Xu, Jing" uniqKey="Xu J" first="Jing" last="Xu">Jing Xu</name>
<name sortKey="Yang, Yalin" sort="Yang, Yalin" uniqKey="Yang Y" first="Yalin" last="Yang">Yalin Yang</name>
<name sortKey="Zhu, Ying" sort="Zhu, Ying" uniqKey="Zhu Y" first="Ying" last="Zhu">Ying Zhu</name>
</country>
</tree>
</affiliations>
</record>
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