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非洲猪瘟病毒晚期启动子的结构:起始区域对TATA序列的需求

Structure of African swine fever virus late promoters: requirement of a TATA sequence at the initiation region.

作者信息

García-Escudero R, Viñuela E

机构信息

Centro de Biología Molecular "Severo Ochoa", Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain.

出版信息

J Virol. 2000 Sep;74(17):8176-82. doi: 10.1128/jvi.74.17.8176-8182.2000.

DOI:10.1128/jvi.74.17.8176-8182.2000
PMID:10933729
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC112352/
Abstract

A number of mutations, including deletions, linker scan substitutions, and point mutations, were performed in the promoter of the late African swine fever virus (ASFV) gene coding for the capsid protein p72. The consequences of the mutations in terms of promoter activity were analyzed by luciferase assays using plasmids transfected into infected cells. The results showed that the promoter function is contained between nucleotides -36 and +5 relative to the transcription initiation site. Moreover, two major essential regions for promoter activity, centered at positions -13 and +3, were located along the 41-bp sequence, the latter mapping in the transcription start site. Sequence alignment with other ASFV late promoters showed homology in the region of transcriptional initiation, where the presence of the sequence TATA was observed in most of the promoters. Substitution of these four residues in three other late viral promoters strongly reduced their respective activities. These results show that cis-acting control elements of ASFV p72 gene transcription are restricted to a short sequence of about 40 bp and suggest that transcription of late genes is initiated around a TATA sequence that would function as an initiator element.

摘要

在编码衣壳蛋白p72的非洲猪瘟病毒(ASFV)晚期基因的启动子中进行了多种突变,包括缺失、接头扫描替换和点突变。通过使用转染到感染细胞中的质粒进行荧光素酶测定,分析了这些突变对启动子活性的影响。结果表明,启动子功能包含在相对于转录起始位点的核苷酸-36至+5之间。此外,沿着41bp序列定位了两个主要的启动子活性必需区域,分别位于-13和+3位置,后者位于转录起始位点。与其他ASFV晚期启动子的序列比对显示,在转录起始区域存在同源性,在大多数启动子中都观察到了TATA序列的存在。在其他三个晚期病毒启动子中替换这四个残基会强烈降低它们各自的活性。这些结果表明,ASFV p72基因转录的顺式作用控制元件局限于约40bp的短序列,并表明晚期基因的转录是围绕一个可作为起始元件的TATA序列起始的。

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