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猿猴病毒40 T抗原及病毒核心复制起点上T抗原起点结合域组装的序列要求。

Sequence requirements for the assembly of simian virus 40 T antigen and the T-antigen origin binding domain on the viral core origin of replication.

作者信息

Kim H Y, Barbaro B A, Joo W S, Prack A E, Sreekumar K R, Bullock P A

机构信息

Department of Biochemistry, Tufts University School of Medicine, Boston, Massachusetts, USA.

出版信息

J Virol. 1999 Sep;73(9):7543-55. doi: 10.1128/JVI.73.9.7543-7555.1999.

Abstract

The regions of the simian virus 40 (SV40) core origin that are required for stable assembly of virally encoded T antigen (T-ag) and the T-ag origin binding domain (T-ag-obd(131-260)) have been determined. Binding of the purified T-ag-obd(131-260) is mediated by interactions with the central region of the core origin, site II. In contrast, T-ag binding and hexamer assembly requires a larger region of the core origin that includes both site II and an additional fragment of DNA that may be positioned on either side of site II. These studies indicate that in the context of T-ag, the origin binding domain can engage the pentanucleotides in site II only if a second region of T-ag interacts with one of the flanking sequences. The requirements for T-ag double-hexamer assembly are complex; the nucleotide cofactor present in the reaction modulates the sequence requirements for oligomerization. Nevertheless, these experiments provide additional evidence that only a subset of the SV40 core origin is required for assembly of T-ag double hexamers.

摘要

已确定猿猴病毒40(SV40)核心起始位点中病毒编码的T抗原(T-ag)稳定组装以及T-ag起始位点结合域(T-ag-obd(131 - 260))所需的区域。纯化的T-ag-obd(131 - 260)的结合是通过与核心起始位点的中心区域即位点II相互作用介导的。相比之下,T-ag结合和六聚体组装需要核心起始位点的更大区域,该区域包括位点II以及可能位于位点II两侧的一段额外DNA片段。这些研究表明,在T-ag的情况下,只有当T-ag的第二个区域与侧翼序列之一相互作用时,起始位点结合域才能与位点II中的五核苷酸结合。T-ag双六聚体组装的要求很复杂;反应中存在的核苷酸辅因子调节寡聚化的序列要求。然而,这些实验提供了额外的证据,即T-ag双六聚体组装仅需要SV40核心起始位点的一个子集。

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