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TAF4/4b与TAF12表现出独特的DNA结合模式,并且是一部分基因核心启动子功能所必需的。

TAF4/4b x TAF12 displays a unique mode of DNA binding and is required for core promoter function of a subset of genes.

作者信息

Gazit Kfir, Moshonov Sandra, Elfakess Rofa, Sharon Michal, Mengus Gabrielle, Davidson Irwin, Dikstein Rivka

机构信息

Department of Biological Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel.

出版信息

J Biol Chem. 2009 Sep 25;284(39):26286-96. doi: 10.1074/jbc.M109.011486. Epub 2009 Jul 27.

Abstract

The major core promoter-binding factor in polymerase II transcription machinery is TFIID, a complex consisting of TBP, the TATA box-binding protein, and 13 to 14 TBP-associated factors (TAFs). Previously we found that the histone H2A-like TAF paralogs TAF4 and TAF4b possess DNA-binding activity. Whether TAF4/TAF4b DNA binding directs TFIID to a specific core promoter element or facilitates TFIID binding to established core promoter elements is not known. Here we analyzed the mode of TAF4b.TAF12 DNA binding and show that this complex binds DNA with high affinity. The DNA length required for optimal binding is approximately 70 bp. Although the complex displays a weak sequence preference, the nucleotide composition is less important than the length of the DNA for high affinity binding. Comparative expression profiling of wild-type and a DNA-binding mutant of TAF4 revealed common core promoter features in the down-regulated genes that include a TATA-box and an Initiator. Further examination of the PEL98 gene from this group showed diminished Initiator activity and TFIID occupancy in TAF4 DNA-binding mutant cells. These findings suggest that DNA binding by TAF4/4b-TAF12 facilitates the association of TFIID with the core promoter of a subset of genes.

摘要

聚合酶II转录机制中的主要核心启动子结合因子是TFIID,它是一种由TBP(TATA盒结合蛋白)以及13到14个TBP相关因子(TAFs)组成的复合体。此前我们发现,组蛋白H2A样TAF旁系同源物TAF4和TAF4b具有DNA结合活性。尚不清楚TAF4/TAF4b的DNA结合是将TFIID导向特定的核心启动子元件,还是促进TFIID与已确定的核心启动子元件结合。在此,我们分析了TAF4b·TAF12的DNA结合模式,结果表明该复合体以高亲和力结合DNA。最佳结合所需的DNA长度约为70bp。尽管该复合体表现出较弱的序列偏好性,但对于高亲和力结合而言,核苷酸组成不如DNA长度重要。对TAF4野生型和DNA结合突变体进行比较表达谱分析,结果显示下调基因中存在共同的核心启动子特征,包括一个TATA盒和一个起始子。对该组中的PEL98基因进一步研究发现,在TAF4 DNA结合突变体细胞中,起始子活性和TFIID占据率降低。这些发现表明,TAF4/4b - TAF12的DNA结合促进了TFIID与一部分基因的核心启动子的结合。

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