• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Spt3 和 Spt8 通过与 TATA 结合蛋白相互作用参与沉默边界的形成。

Spt3 and Spt8 Are Involved in the Formation of a Silencing Boundary by Interacting with TATA-Binding Protein.

机构信息

Department of Applied Chemistry & Biotechnology, Graduate School of Engineering, University of Fukui, Fukui 910-8507, Japan.

Japan Society for the Promotion of Science for Young Scientists (JSPS), Tokyo 102-0083, Japan.

出版信息

Biomolecules. 2023 Mar 30;13(4):619. doi: 10.3390/biom13040619.

DOI:10.3390/biom13040619
PMID:37189367
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10136053/
Abstract

In , a heterochromatin-like chromatin structure called the silencing region is present at the telomere as a complex of Sir2, Sir3, and Sir4. Although spreading of the silencing region is blocked by histone acetylase-mediated boundary formation, the details of the factors and mechanisms involved in the spread and formation of the boundary at each telomere are unknown. Here, we show that Spt3 and Spt8 block the spread of the silencing regions. Spt3 and Spt8 are members of the Spt-Ada-Gcn5-acetyltransferase (SAGA) complex, which has histone acetyltransferase activity. We performed microarray analysis of the transcriptome of and strains and RT-qPCR analysis of the transcript levels of genes from the subtelomeric region in mutants in which the interaction of Spt3 with TATA-binding protein (TBP) is altered. The results not only indicated that both Spt3 and Spt8 are involved in TBP-mediated boundary formation on the right arm of chromosome III, but also that boundary formation in this region is DNA sequence independent. Although both Spt3 and Spt8 interact with TBP, Spt3 had a greater effect on genome-wide transcription. Mutant analysis showed that the interaction between Spt3 and TBP plays an important role in the boundary formation.

摘要

在 中,端粒处存在一种类似于异染色质的染色质结构,称为沉默区域,它是由 Sir2、Sir3 和 Sir4 组成的复合物。尽管组蛋白乙酰转移酶介导的边界形成阻止了沉默区域的扩散,但每个端粒处涉及的边界扩散和形成的因素和机制的细节尚不清楚。在这里,我们表明 Spt3 和 Spt8 阻止了沉默区域的扩散。Spt3 和 Spt8 是 Spt-Ada-Gcn5-乙酰转移酶(SAGA)复合物的成员,该复合物具有组蛋白乙酰转移酶活性。我们对 和 菌株的转录组进行了微阵列分析,并对 TBP 相互作用改变的突变体中来自端粒区的基因的转录水平进行了 RT-qPCR 分析。结果不仅表明 Spt3 和 Spt8 都参与了 TBP 在染色体 III 右臂上的边界形成,而且该区域的边界形成与 DNA 序列无关。尽管 Spt3 和 Spt8 都与 TBP 相互作用,但 Spt3 对全基因组转录的影响更大。突变体分析表明,Spt3 与 TBP 之间的相互作用在边界形成中起着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823a/10136053/42a332de1ecc/biomolecules-13-00619-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823a/10136053/9b0347f018a1/biomolecules-13-00619-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823a/10136053/f64f91392dc1/biomolecules-13-00619-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823a/10136053/42c4cd73e5af/biomolecules-13-00619-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823a/10136053/2ec07dc1b3c5/biomolecules-13-00619-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823a/10136053/9fc03d0d14f9/biomolecules-13-00619-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823a/10136053/9c8b327c713a/biomolecules-13-00619-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823a/10136053/42a332de1ecc/biomolecules-13-00619-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823a/10136053/9b0347f018a1/biomolecules-13-00619-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823a/10136053/f64f91392dc1/biomolecules-13-00619-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823a/10136053/42c4cd73e5af/biomolecules-13-00619-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823a/10136053/2ec07dc1b3c5/biomolecules-13-00619-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823a/10136053/9fc03d0d14f9/biomolecules-13-00619-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823a/10136053/9c8b327c713a/biomolecules-13-00619-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/823a/10136053/42a332de1ecc/biomolecules-13-00619-g007.jpg

相似文献

1
Spt3 and Spt8 Are Involved in the Formation of a Silencing Boundary by Interacting with TATA-Binding Protein.Spt3 和 Spt8 通过与 TATA 结合蛋白相互作用参与沉默边界的形成。
Biomolecules. 2023 Mar 30;13(4):619. doi: 10.3390/biom13040619.
2
Characterization of new Spt3 and TATA-binding protein mutants of Saccharomyces cerevisiae: Spt3 TBP allele-specific interactions and bypass of Spt8.酿酒酵母新的Spt3和TATA结合蛋白突变体的特征:Spt3 TBP等位基因特异性相互作用及Spt8的旁路效应
Genetics. 2007 Dec;177(4):2007-17. doi: 10.1534/genetics.107.081976.
3
Regulation of TATA-binding protein binding by the SAGA complex and the Nhp6 high-mobility group protein.SAGA复合物和Nhp6高迁移率族蛋白对TATA结合蛋白结合的调控。
Mol Cell Biol. 2003 Mar;23(6):1910-21. doi: 10.1128/MCB.23.6.1910-1921.2003.
4
Inhibition of TATA-binding protein function by SAGA subunits Spt3 and Spt8 at Gcn4-activated promoters.在Gcn4激活的启动子处,SAGA亚基Spt3和Spt8对TATA结合蛋白功能的抑制作用。
Mol Cell Biol. 2000 Jan;20(2):634-47. doi: 10.1128/MCB.20.2.634-647.2000.
5
The Saccharomyces cerevisiae SPT8 gene encodes a very acidic protein that is functionally related to SPT3 and TATA-binding protein.酿酒酵母的SPT8基因编码一种酸性很强的蛋白质,该蛋白质在功能上与SPT3及TATA结合蛋白相关。
Genetics. 1994 Jul;137(3):647-57. doi: 10.1093/genetics/137.3.647.
6
Site-specific cross-linking of TBP in vivo and in vitro reveals a direct functional interaction with the SAGA subunit Spt3.体内和体外TBP的位点特异性交联揭示了其与SAGA亚基Spt3的直接功能相互作用。
Genes Dev. 2008 Nov 1;22(21):2994-3006. doi: 10.1101/gad.1724408.
7
A human SPT3-TAFII31-GCN5-L acetylase complex distinct from transcription factor IID.一种不同于转录因子IID的人类SPT3-TAFII31-GCN5-L乙酰化酶复合物。
J Biol Chem. 1998 Sep 11;273(37):23781-5. doi: 10.1074/jbc.273.37.23781.
8
Functional organization of the yeast SAGA complex: distinct components involved in structural integrity, nucleosome acetylation, and TATA-binding protein interaction.酵母SAGA复合物的功能组织:参与结构完整性、核小体乙酰化及TATA结合蛋白相互作用的不同组分
Mol Cell Biol. 1999 Jan;19(1):86-98. doi: 10.1128/MCB.19.1.86.
9
Mapping the deubiquitination module within the SAGA complex.绘制SAGA复合物中的去泛素化模块
Structure. 2014 Nov 4;22(11):1553-9. doi: 10.1016/j.str.2014.07.017.
10
Prp5-Spt8/Spt3 interaction mediates a reciprocal coupling between splicing and transcription.Prp5-Spt8/Spt3 相互作用介导剪接和转录之间的相互偶联。
Nucleic Acids Res. 2020 Jun 19;48(11):5799-5813. doi: 10.1093/nar/gkaa311.

引用本文的文献

1
CCL22 as a diagnostic and prognostic biomarker for pediatric-onset systemic lupus erythematosus.CCL22作为儿童期系统性红斑狼疮的诊断和预后生物标志物。
Clin Exp Med. 2025 Jul 8;25(1):235. doi: 10.1007/s10238-025-01790-0.
2
GTP-dependent regulation of heterochromatin fluctuations at subtelomeric regions in Saccharomyces cerevisiae.酿酒酵母亚端粒区域异染色质波动的GTP依赖性调控。
Genes Cells. 2024 Mar;29(3):217-230. doi: 10.1111/gtc.13094. Epub 2024 Jan 16.

本文引用的文献

1
Conformational landscape of the yeast SAGA complex as revealed by cryo-EM.冷冻电镜解析酵母 SAGA 复合物的构象景观。
Sci Rep. 2022 Jul 19;12(1):12306. doi: 10.1038/s41598-022-16391-0.
2
The regional sequestration of heterochromatin structural proteins is critical to form and maintain silent chromatin.异染色质结构蛋白的区域性隔离对于形成和维持沉默染色质至关重要。
Epigenetics Chromatin. 2022 Jan 31;15(1):5. doi: 10.1186/s13072-022-00435-w.
3
Spreading-dependent or independent Sir2-mediated gene silencing in budding yeast.芽殖酵母中依赖或不依赖扩散的Sir2介导的基因沉默
Genes Genomics. 2022 Mar;44(3):359-367. doi: 10.1007/s13258-021-01203-y. Epub 2022 Jan 16.
4
The biochemical and genetic discovery of the SAGA complex.SAGA 复合物的生化和遗传发现。
Biochim Biophys Acta Gene Regul Mech. 2021 Feb;1864(2):194669. doi: 10.1016/j.bbagrm.2020.194669. Epub 2020 Dec 16.
5
Architecture of the multi-functional SAGA complex and the molecular mechanism of holding TBP.多功能 SAGA 复合物的结构和结合 TBP 的分子机制。
FEBS J. 2021 May;288(10):3135-3147. doi: 10.1111/febs.15563. Epub 2020 Sep 29.
6
Structure of SAGA and mechanism of TBP deposition on gene promoters.SAGA 的结构和 TBP 在基因启动子上沉积的机制。
Nature. 2020 Jan;577(7792):711-716. doi: 10.1038/s41586-020-1944-2. Epub 2020 Jan 22.
7
Structure of the transcription coactivator SAGA.转录共激活因子 SAGA 的结构。
Nature. 2020 Jan;577(7792):717-720. doi: 10.1038/s41586-020-1933-5. Epub 2020 Jan 22.
8
Architecture of SAGA complex.SAGA复合物的结构
Cell Discov. 2019 May 7;5:25. doi: 10.1038/s41421-019-0094-x. eCollection 2019.
9
Molecular mechanisms that distinguish TFIID housekeeping from regulatable SAGA promoters.区分TFIID管家型启动子与可调节SAGA启动子的分子机制。
EMBO J. 2017 Feb 1;36(3):274-290. doi: 10.15252/embj.201695621. Epub 2016 Dec 15.
10
Four domains of Ada1 form a heterochromatin boundary through different mechanisms.Ada1的四个结构域通过不同机制形成一个异染色质边界。
Genes Cells. 2016 Oct;21(10):1125-1136. doi: 10.1111/gtc.12421. Epub 2016 Sep 20.