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Studies on transcription controls operating in archaeal virus-host systems: regulation of transcription of genomes of the rudiviruses SIRV1 and SIRV2, and the lipothrixvirus SIFV of the hyperthermophilic archaeaon Sulfolobus

Studies on transcription controls operating in archaeal virus-host systems: regulation of transcription of genomes of the rudiviruses SIRV1 and SIRV2, and the lipothrixvirus SIFV of the hyperthermophilic archaeaon Sulfolobus
古细菌病毒宿主系统中转录控制的研究:鲁迪病毒 SIRV1 和 SIRV2 以及超嗜热古细菌硫化叶菌的脂丝病毒 SIFV 基因组转录的调节
批准号:
5314438
负责人:
Dr. David Prangishvili
金额:
$0.0万
依托单位:
依托单位国家:
德国
项目类别:
Priority Programmes
财政年份:
2001
资助国家:
德国
项目状态:
已结题
起止时间:
2000-12-31 至 2006-12-31

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中文摘要
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英文摘要
A pair of rod-shaped viruses SIRV1 and SIRV2 of hyperthermophilic Sulfolobus, the genomes of which have been recently completely sequenced, is an attractive and unique model for unravelling mechanisms, controls and signal structures involved in gene expression in Archaea. The virus SIRV1 responds to changes of a host in a way unusual for DNA viruses by extensive and rapid accumulation of point mutations in the genome. This allows rapid selection of new virus variants adapted to a new host, coinciding with a recovery of high fidelity of replication. In contrast to the genome of SIRV1, the genome of SIRV2, which is highly homologous to the latter, however, 3.2 kb longer, remains unchanged in the same hosts. In order to understand the SIRV1-specific mutator system and its control we plan to study transcription and replication of the genomes of the two viruses. Comparative studies of transcripts of the genomes of SIRV1 and SIRV2 in different hosts will enable us to identify candidate genes that are involved in a response to changes of host species, and those which cause differences in the behaviour of the viruses under such conditions. These genes will be selectively disrupted, or deleted/introduced from/into the DNAs of the viruses by constructing recombinant DNA molecules consisting of different portions of the genomes of the two viruses in a way not affecting essential viral functions. Transfection of an appropriate host with these DNAs and studies on their replication and transcription will shed light on functions of proteins encoded by the genes and controls of their expression. The studies will also enable to identify ORFs which are nonessential for virus function, and lay the basis for the development of a transformation vector based on the virus DNAs.
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