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转录因子MAZ和Sp1对腺病毒主要晚期启动子的激活作用。

Activation of the adenovirus major late promoter by transcription factors MAZ and Sp1.

作者信息

Parks C L, Shenk T

机构信息

Department of Molecular Biology, Howard Hughes Medical Institute, Princeton University, New Jersey 08544-1014, USA.

出版信息

J Virol. 1997 Dec;71(12):9600-7. doi: 10.1128/JVI.71.12.9600-9607.1997.

Abstract

Multiple binding sites for the transcription factors MAZ and Sp1 within the adenovirus type 5 major late promoter have been identified by DNase I protection studies. In the proximal region of the promoter, both MAZ and Sp1 interact with GC-rich sequences flanking the TATA box. Two MAZ binding sites are centered at -18 and -36 relative to the transcriptional initiation site. Sp1 bound only to the -18 GC-rich sequence. Several sites of interaction were also evident in the distal region of the promoter. Both MAZ and Sp1 interacted with a sequence centered at -166, and MAZ bound weakly to an additional site centered at -130. Overexpression of MAZ or Sp1 activated expression from the major late promoter in transient expression assays. Mutational analysis of the GC-rich sequences in the major late promoter suggested that a primary target of MAZ activation is the GC-rich sequences flanking the TATA sequence, whereas Sp1 requires the distal GC-rich sequence elements to stimulate gene expression. This activation is enhanced by the adenovirus E1A protein, and evidence for interaction between E1A and both transcription factors was obtained by using an immunoprecipitation assay. Activation by MAZ and Sp1 also was observed in transfection studies using the complete adenovirus type 5 genome as the target. Increased levels of late mRNA from both the L1 and L5 regions were observed when MAZ or Sp1 expression plasmids were transfected with viral DNA. Unexpectedly, activation of the major late promoter by MAZ and Sp1 was detected irrespective of whether the viral DNA could replicate.

摘要

通过DNA酶I保护研究,已在腺病毒5型主要晚期启动子内鉴定出转录因子MAZ和Sp1的多个结合位点。在启动子的近端区域,MAZ和Sp1均与TATA框两侧富含GC的序列相互作用。两个MAZ结合位点相对于转录起始位点分别位于-18和-36处。Sp1仅与-18富含GC的序列结合。在启动子的远端区域也有几个相互作用位点明显可见。MAZ和Sp1均与一个以-166为中心的序列相互作用,并且MAZ与另一个以-130为中心的位点弱结合。在瞬时表达测定中,MAZ或Sp1的过表达激活了主要晚期启动子的表达。对主要晚期启动子中富含GC的序列进行突变分析表明,MAZ激活的主要靶标是TATA序列两侧富含GC的序列,而Sp1需要远端富含GC的序列元件来刺激基因表达。腺病毒E1A蛋白可增强这种激活作用,并且通过免疫沉淀试验获得了E1A与这两种转录因子之间相互作用的证据。在以完整的腺病毒5型基因组为靶标的转染研究中也观察到了MAZ和Sp1的激活作用。当MAZ或Sp1表达质粒与病毒DNA一起转染时,观察到来自L1和L5区域的晚期mRNA水平升高。出乎意料的是,无论病毒DNA是否能够复制,均检测到MAZ和Sp1对主要晚期启动子的激活作用。

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本文引用的文献

2
Crystal structure of the yeast TFIIA/TBP/DNA complex.
Science. 1996 May 10;272(5263):830-6. doi: 10.1126/science.272.5263.830.
3
The serotonin 1a receptor gene contains a TATA-less promoter that responds to MAZ and Sp1.
J Biol Chem. 1996 Feb 23;271(8):4417-30. doi: 10.1074/jbc.271.8.4417.
4
Crystal structure of a yeast TFIIA/TBP/DNA complex.
Nature. 1996 May 9;381(6578):127-51. doi: 10.1038/381127a0.
5
Crystal structure of a TFIIB-TBP-TATA-element ternary complex.
Nature. 1995 Sep 14;377(6545):119-28. doi: 10.1038/377119a0.
6
DNA binding sites for the transcriptional activator/repressor YY1.
Nucleic Acids Res. 1995 Nov 11;23(21):4457-65. doi: 10.1093/nar/23.21.4457.
7
DNA replication and the early to late transition in adenovirus infection.
Cell. 1980 Nov;22(2 Pt 2):523-33. doi: 10.1016/0092-8674(80)90362-1.
9
Generation and functional analyses for base-substitution mutants of the adenovirus 2 major late promoter.
Nucleic Acids Res. 1984 Dec 21;12(24):9309-21. doi: 10.1093/nar/12.24.9309.
10
The genetic analysis of recombination using adenovirus overlapping terminal DNA fragments.
Virology. 1983 Feb;125(1):175-93. doi: 10.1016/0042-6822(83)90072-7.

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