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CCR4-NOT蛋白与酵母中TATA结合蛋白(TBP)及其相关因子的功能相互作用。

Functional interaction of CCR4-NOT proteins with TATAA-binding protein (TBP) and its associated factors in yeast.

作者信息

Badarinarayana V, Chiang Y C, Denis C L

机构信息

Department of Biochemistry and Molecular Biology, University of New Hampshire, Durham, New Hampshire 03824, USA.

出版信息

Genetics. 2000 Jul;155(3):1045-54. doi: 10.1093/genetics/155.3.1045.

Abstract

The CCR4-NOT transcriptional regulatory complex affects expression of a number of genes both positively and negatively. We report here that components of the CCR4-NOT complex functionally and physically interact with TBP and TBP-associated factors. First, mutations in CCR4-NOT components suppressed the his4-912delta insertion in a manner similar to that observed for the defective TBP allele spt15-122. Second, using modified HIS3 promoter derivatives containing specific mutations within the TATA sequence, we found that the NOT proteins were general repressors that disrupt TBP function irrespective of the DNA sequence. Third, increasing the dosage of NOT1 specifically inhibited the ability of spt15-122 to suppress the his4-912delta insertion but did not affect the Spt- phenotype of spt3 or spt10 at this locus. Fourth, spt3, spt8, and spt15-21 alleles (all involved in affecting interaction of SPT3 with TBP) suppressed ccr4 and caf1 defects. Finally, we show that NOT2 and NOT5 can be immunoprecipitated by TBP. NOT5 was subsequently shown to associate with TBP and TAFs and this association was dependent on the integrity of TFIID. These genetic and physical interactions indicate that one role of the CCR4-NOT proteins is to inhibit functional TBP-DNA interactions, perhaps by interacting with and modulating the function of TFIID.

摘要

CCR4-NOT转录调控复合物对许多基因的表达具有正向和负向影响。我们在此报告,CCR4-NOT复合物的组分在功能和物理上与TBP及TBP相关因子相互作用。首先,CCR4-NOT组分中的突变以类似于有缺陷的TBP等位基因spt15-122所观察到的方式抑制了his4-912delta插入。其次,使用在TATA序列内含有特定突变的修饰HIS3启动子衍生物,我们发现NOT蛋白是普遍的阻遏物,无论DNA序列如何都能破坏TBP功能。第三,增加NOT1的剂量特异性地抑制了spt15-122抑制his4-912delta插入的能力,但在此位点不影响spt3或spt10的Spt-表型。第四,spt3、spt8和spt15-21等位基因(均参与影响SPT3与TBP的相互作用)抑制了ccr4和caf1缺陷。最后,我们表明NOT2和NOT5可被TBP免疫沉淀。随后显示NOT5与TBP和TAF相关联,并且这种关联依赖于TFIID的完整性。这些遗传和物理相互作用表明,CCR4-NOT蛋白的一个作用可能是通过与TFIID相互作用并调节其功能来抑制功能性TBP-DNA相互作用。

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