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Nhp6、Gcn5和Swi/Snf复合物在刺激TATA结合蛋白-TFIIA-DNA复合物形成中的作用。

Role for Nhp6, Gcn5, and the Swi/Snf complex in stimulating formation of the TATA-binding protein-TFIIA-DNA complex.

作者信息

Biswas Debabrata, Imbalzano Anthony N, Eriksson Peter, Yu Yaxin, Stillman David J

机构信息

Department of Pathology, University of Utah Health Sciences Center, Salt Lake City, USA.

出版信息

Mol Cell Biol. 2004 Sep;24(18):8312-21. doi: 10.1128/MCB.24.18.8312-8321.2004.

Abstract

The TATA-binding protein (TBP), TFIIA, and TFIIB interact with promoter DNA to form a complex required for transcriptional initiation, and many transcriptional regulators function by either stimulating or inhibiting formation of this complex. We have recently identified TBP mutants that are viable in wild-type cells but lethal in the absence of the Nhp6 architectural transcription factor. Here we show that many of these TBP mutants were also lethal in strains with disruptions of either GCN5, encoding the histone acetyltransferase in the SAGA complex, or SWI2, encoding the catalytic subunit of the Swi/Snf chromatin remodeling complex. These synthetic lethalities could be suppressed by overexpression of TOA1 and TOA2, the genes encoding TFIIA. We also used TFIIA mutants that eliminated in vitro interactions with TBP. These viable TFIIA mutants were lethal in strains lacking Gcn5, Swi2, or Nhp6. These lethalities could be suppressed by overexpression of TBP or Nhp6, suggesting that these coactivators stimulate formation of the TBP-TFIIA-DNA complex. In vitro studies have previously shown that TBP binds very poorly to a TATA sequence within a nucleosome but that Swi/Snf stimulates binding of TBP and TFIIA. In vitro binding experiments presented here show that histone acetylation facilitates TBP binding to a nucleosomal binding site and that Nhp6 stimulates formation of a TBP-TFIIA-DNA complex. Consistent with the idea that Nhp6, Gcn5, and Swi/Snf have overlapping functions in vivo, nhp6a nhp6b gcn5 mutants had a severe growth defect, and mutations in both nhp6a nhp6b swi2 and gcn5 swi2 strains were lethal.

摘要

TATA 结合蛋白(TBP)、TFIIA 和 TFIIB 与启动子 DNA 相互作用,形成转录起始所需的复合物,许多转录调节因子通过刺激或抑制该复合物的形成发挥作用。我们最近鉴定出了一些 TBP 突变体,它们在野生型细胞中能够存活,但在缺乏 Nhp6 结构转录因子时是致死的。在这里我们表明,许多这些 TBP 突变体在编码 SAGA 复合物中组蛋白乙酰转移酶的 GCN5 或编码 Swi/Snf 染色质重塑复合物催化亚基的 SWI2 被破坏的菌株中也是致死的。这些合成致死性可以通过编码 TFIIA 的基因 TOA1 和 TOA2 的过表达来抑制。我们还使用了消除了与 TBP 的体外相互作用的 TFIIA 突变体。这些可存活的 TFIIA 突变体在缺乏 Gcn5、Swi2 或 Nhp6 的菌株中是致死的。这些致死性可以通过 TBP 或 Nhp6 的过表达来抑制,这表明这些共激活因子刺激 TBP-TFIIA-DNA 复合物的形成。先前的体外研究表明,TBP 与核小体内的 TATA 序列结合非常差,但 Swi/Snf 刺激 TBP 和 TFIIA 的结合。这里展示的体外结合实验表明组蛋白乙酰化促进 TBP 与核小体结合位点的结合,并且 Nhp6 刺激 TBP-TFIIA-DNA 复合物的形成。与 Nhp6、Gcn5 和 Swi/Snf 在体内具有重叠功能的观点一致,nhp6a nhp6b gcn5 突变体有严重的生长缺陷,并且 nhp6a nhp6b swi2 和 gcn5 swi2 菌株中的突变都是致死的。

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本文引用的文献

1
TATA-binding protein mutants that are lethal in the absence of the Nhp6 high-mobility-group protein.
Mol Cell Biol. 2004 Jul;24(14):6419-29. doi: 10.1128/MCB.24.14.6419-6429.2004.
2
pRS yeast vectors with a LYS2 marker.
Biotechniques. 2004 Feb;36(2):212-3. doi: 10.2144/04362BM01.
3
Nhp6 facilitates Aft1 binding and Ssn6 recruitment, both essential for FRE2 transcriptional activation.
EMBO J. 2004 Jan 28;23(2):333-42. doi: 10.1038/sj.emboj.7600043. Epub 2004 Jan 22.
4
The protein network of HIV budding.
Cell. 2003 Sep 19;114(6):701-13. doi: 10.1016/s0092-8674(03)00714-1.
5
Recent advances in understanding chromatin remodeling by Swi/Snf complexes.
Curr Opin Genet Dev. 2003 Apr;13(2):136-42. doi: 10.1016/s0959-437x(03)00022-4.
6
Priming the nucleosome: a role for HMGB proteins?
EMBO Rep. 2003 Feb;4(2):131-6. doi: 10.1038/sj.embor.embor741.
7
Regulation of TATA-binding protein binding by the SAGA complex and the Nhp6 high-mobility group protein.
Mol Cell Biol. 2003 Mar;23(6):1910-21. doi: 10.1128/MCB.23.6.1910-1921.2003.
8
Evidence that Swi/Snf directly represses transcription in S. cerevisiae.
Genes Dev. 2002 Sep 1;16(17):2231-6. doi: 10.1101/gad.1009902.
9
Specificity of gene regulation.
Cell. 2002 May 3;109(3):267-70. doi: 10.1016/s0092-8674(02)00740-7.
10
Cooperation between complexes that regulate chromatin structure and transcription.
Cell. 2002 Feb 22;108(4):475-87. doi: 10.1016/s0092-8674(02)00654-2.

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