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卡波西肉瘤相关疱疹病毒ORF57在病毒RNA加工中的作用

Kaposi's sarcoma-associated herpesvirus ORF57 in viral RNA processing.

作者信息

Majerciak Vladimir, Zheng Zhi-Ming

机构信息

HIV and AIDS Malignancy Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892-1868, USA.

出版信息

Front Biosci (Landmark Ed). 2009 Jan 1;14(4):1516-28. doi: 10.2741/3322.

Abstract

Kaposi's sarcoma-associated herpesvirus (KSHV) ORF57 (MTA, mRNA transcript accumulation) is a multifunctional regulator of the expression of viral lytic genes. KSHV ORF57 is expressed during viral lytic infection and is essential for virus production. Like its homologues in the herpesvirus family, ORF57 promotes the accumulation (stabilization) and export of viral intronless RNA transcripts by a mechanism which remains to be defined. The ORF57-Aly/REF interaction plays only a small role in viral RNA export. Although other members of the family generally inhibit the splicing of cellular RNAs, KSHV ORF57 and EBV EB2, in sharp contrast, stimulate viral RNA splicing for the expression of viral intron-containing genes. The functions of KSHV ORF57 are independent of transcription and of other viral proteins; instead, these functions always rely on cellular components and occur in various protein-RNA complexes. ORF57 may synergize with KSHV ORF50 to transactivate a subset of viral promoters by an unknown mechanism. Thus, some functions of ORF57 have been conserved while others have diverged from its homologues as ORF57 adapted over evolution to KSHV biology and pathogenesis.

摘要

卡波西肉瘤相关疱疹病毒(KSHV)的ORF57(MTA,mRNA转录积累)是病毒裂解基因表达的多功能调节因子。KSHV ORF57在病毒裂解感染期间表达,对病毒产生至关重要。与其在疱疹病毒家族中的同源物一样,ORF57通过一种尚待确定的机制促进病毒无内含子RNA转录本的积累(稳定)和输出。ORF57与Aly/REF的相互作用在病毒RNA输出中仅起很小的作用。虽然该家族的其他成员通常会抑制细胞RNA的剪接,但与之形成鲜明对比的是,KSHV ORF57和EBV EB2会刺激病毒RNA剪接,以表达含病毒内含子的基因。KSHV ORF57的功能独立于转录和其他病毒蛋白;相反,这些功能总是依赖于细胞成分,并发生在各种蛋白质-RNA复合物中。ORF57可能通过一种未知机制与KSHV ORF50协同作用,反式激活一部分病毒启动子。因此,随着ORF57在进化过程中适应KSHV的生物学特性和发病机制,其一些功能得以保留,而另一些功能则与其同源物有所不同。

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