• 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

一般转录因子IIA、IIB、IIF和IIE是从人U1小核RNA启动子进行RNA聚合酶II转录所必需的。

The general transcription factors IIA, IIB, IIF, and IIE are required for RNA polymerase II transcription from the human U1 small nuclear RNA promoter.

作者信息

Kuhlman T C, Cho H, Reinberg D, Hernandez N

机构信息

Graduate Program in Molecular and Cellular Pharmacology, State University of New York at Stony Brook, Stony Brook, New York 11794, USA.

出版信息

Mol Cell Biol. 1999 Mar;19(3):2130-41. doi: 10.1128/MCB.19.3.2130.

DOI:10.1128/MCB.19.3.2130
PMID:10022900
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC84006/
Abstract

RNA polymerase II transcribes the mRNA-encoding genes and the majority of the small nuclear RNA (snRNA) genes. The formation of a minimal functional transcription initiation complex on a TATA-box-containing mRNA promoter has been well characterized and involves the ordered assembly of a number of general transcription factors (GTFs), all of which have been either cloned or purified to near homogeneity. In the human RNA polymerase II snRNA promoters, a single element, the proximal sequence element (PSE), is sufficient to direct basal levels of transcription in vitro. The PSE is recognized by the basal transcription complex SNAPc. SNAPc, which is not required for transcription from mRNA-type RNA polymerase II promoters such as the adenovirus type 2 major late (Ad2ML) promoter, is thought to recruit TATA binding protein (TBP) and nucleate the assembly of the snRNA transcription initiation complex, but little is known about which GTFs other than TBP are required. Here we show that the GTFs IIA, IIB, IIF, and IIE are required for efficient RNA polymerase II transcription from snRNA promoters. Thus, although the factors that recognize the core elements of RNA polymerase II mRNA and snRNA-type promoters differ, they mediate the recruitment of many common GTFs.

摘要

RNA聚合酶II转录编码mRNA的基因以及大多数小核RNA(snRNA)基因。在含TATA框的mRNA启动子上形成最小功能转录起始复合物的过程已得到充分表征,涉及多种通用转录因子(GTF)的有序组装,所有这些转录因子都已被克隆或纯化至近乎均一。在人类RNA聚合酶II的snRNA启动子中,单个元件,即近端序列元件(PSE),足以在体外指导基础水平的转录。PSE被基础转录复合物SNAPc识别。SNAPc对于从mRNA型RNA聚合酶II启动子(如腺病毒2型主要晚期(Ad2ML)启动子)进行转录不是必需的,它被认为可招募TATA结合蛋白(TBP)并启动snRNA转录起始复合物的组装,但对于除TBP之外还需要哪些GTF却知之甚少。在这里,我们表明GTF IIA、IIB、IIF和IIE是snRNA启动子高效进行RNA聚合酶II转录所必需的。因此,尽管识别RNA聚合酶II mRNA和snRNA型启动子核心元件的因子不同,但它们介导了许多常见GTF的招募。

相似文献

1
The general transcription factors IIA, IIB, IIF, and IIE are required for RNA polymerase II transcription from the human U1 small nuclear RNA promoter.一般转录因子IIA、IIB、IIF和IIE是从人U1小核RNA启动子进行RNA聚合酶II转录所必需的。
Mol Cell Biol. 1999 Mar;19(3):2130-41. doi: 10.1128/MCB.19.3.2130.
2
Targeting TBP to a non-TATA box cis-regulatory element: a TBP-containing complex activates transcription from snRNA promoters through the PSE.将TBP靶向非TATA盒顺式调控元件:一种含TBP的复合物通过PSE激活来自snRNA启动子的转录。
Genes Dev. 1993 Aug;7(8):1535-48. doi: 10.1101/gad.7.8.1535.
3
Mechanism of selective recruitment of RNA polymerases II and III to snRNA gene promoters.RNA 聚合酶 II 和 III 选择性募集到 snRNA 基因启动子的机制。
Genes Dev. 2018 May 1;32(9-10):711-722. doi: 10.1101/gad.314245.118. Epub 2018 May 21.
4
Cloning of two proximal sequence element-binding transcription factor subunits (gamma and delta) that are required for transcription of small nuclear RNA genes by RNA polymerases II and III and interact with the TATA-binding protein.克隆两个近端序列元件结合转录因子亚基(γ和δ),它们是RNA聚合酶II和III转录小核RNA基因所必需的,并与TATA结合蛋白相互作用。
Mol Cell Biol. 1996 Jan;16(1):1-9. doi: 10.1128/MCB.16.1.1.
5
The SNAP45 subunit of the small nuclear RNA (snRNA) activating protein complex is required for RNA polymerase II and III snRNA gene transcription and interacts with the TATA box binding protein.小核RNA(snRNA)激活蛋白复合体的SNAP45亚基是RNA聚合酶II和III的snRNA基因转录所必需的,并且可与TATA盒结合蛋白相互作用。
Proc Natl Acad Sci U S A. 1996 Apr 30;93(9):4289-93. doi: 10.1073/pnas.93.9.4289.
6
Structural basis of SNAPc-dependent snRNA transcription initiation by RNA polymerase II.RNA 聚合酶 II 依赖 SNAPc 的 snRNA 转录起始的结构基础。
Nat Struct Mol Biol. 2022 Dec;29(12):1159-1169. doi: 10.1038/s41594-022-00857-w. Epub 2022 Nov 24.
7
Proximal sequence element-binding transcription factor (PTF) is a multisubunit complex required for transcription of both RNA polymerase II- and RNA polymerase III-dependent small nuclear RNA genes.近端序列元件结合转录因子(PTF)是一种多亚基复合物,是RNA聚合酶II和RNA聚合酶III依赖性小核RNA基因转录所必需的。
Mol Cell Biol. 1995 Apr;15(4):2019-27. doi: 10.1128/MCB.15.4.2019.
8
Common and unique transcription factor requirements of human U1 and U6 snRNA genes.人类U1和U6 snRNA基因常见和独特的转录因子需求
EMBO J. 1993 Sep;12(9):3573-85. doi: 10.1002/j.1460-2075.1993.tb06031.x.
9
Different human TFIIIB activities direct RNA polymerase III transcription from TATA-containing and TATA-less promoters.不同的人类TFIIIB活性指导RNA聚合酶III从含TATA和不含TATA的启动子进行转录。
Genes Dev. 2000 Oct 15;14(20):2650-63. doi: 10.1101/gad.836400.
10
Cooperation between small nuclear RNA-activating protein complex (SNAPC) and TATA-box-binding protein antagonizes protein kinase CK2 inhibition of DNA binding by SNAPC.小核RNA激活蛋白复合体(SNAPC)与TATA框结合蛋白之间的合作拮抗蛋白激酶CK2对SNAPC与DNA结合的抑制作用。
J Biol Chem. 2005 Jul 29;280(30):27697-704. doi: 10.1074/jbc.M503206200. Epub 2005 Jun 14.

引用本文的文献

1
CAPTURE of the Human U2 snRNA Genes Expands the Repertoire of Associated Factors.人类U2小核RNA基因的捕获扩展了相关因子的种类。
Biomolecules. 2022 May 14;12(5):704. doi: 10.3390/biom12050704.
2
Exosomal miR-106a-5p accelerates the progression of nasopharyngeal carcinoma through FBXW7-mediated TRIM24 degradation.外泌体 miR-106a-5p 通过 FBXW7 介导的 TRIM24 降解加速鼻咽癌的进展。
Cancer Sci. 2022 May;113(5):1652-1668. doi: 10.1111/cas.15337. Epub 2022 Mar 29.
3
Mediator Is Essential for Small Nuclear and Nucleolar RNA Transcription in Yeast.中介体对于酵母中小核和核仁 RNA 转录是必需的。
Mol Cell Biol. 2018 Nov 28;38(24). doi: 10.1128/MCB.00296-18. Print 2018 Dec 15.
4
Mechanism of selective recruitment of RNA polymerases II and III to snRNA gene promoters.RNA 聚合酶 II 和 III 选择性募集到 snRNA 基因启动子的机制。
Genes Dev. 2018 May 1;32(9-10):711-722. doi: 10.1101/gad.314245.118. Epub 2018 May 21.
5
Salt Stress and CTD PHOSPHATASE-LIKE4 Mediate the Switch between Production of Small Nuclear RNAs and mRNAs.盐胁迫和 CTD 磷酸酶样 4 介导小核 RNA 和 mRNAs 之间产生的转换。
Plant Cell. 2017 Dec;29(12):3214-3233. doi: 10.1105/tpc.17.00331. Epub 2017 Nov 1.
6
Regulation of expression of human RNA polymerase II-transcribed snRNA genes.人类 RNA 聚合酶 II 转录的 snRNA 基因表达的调控。
Open Biol. 2017 Jun;7(6). doi: 10.1098/rsob.170073.
7
Genome-wide computational prediction and analysis of core promoter elements across plant monocots and dicots.跨单子叶植物和双子叶植物核心启动子元件的全基因组计算预测与分析
PLoS One. 2013 Oct 29;8(10):e79011. doi: 10.1371/journal.pone.0079011. eCollection 2013.
8
Genomic study of RNA polymerase II and III SNAPc-bound promoters reveals a gene transcribed by both enzymes and a broad use of common activators.对 RNA 聚合酶 II 和 III SNAPc 结合启动子的基因组研究揭示了一种由两种酶转录的基因和广泛使用的通用激活子。
PLoS Genet. 2012;8(11):e1003028. doi: 10.1371/journal.pgen.1003028. Epub 2012 Nov 15.
9
Requirement for SNAPC1 in transcriptional responsiveness to diverse extracellular signals.SNAPC1 在转录响应多种细胞外信号中的要求。
Mol Cell Biol. 2012 Nov;32(22):4642-50. doi: 10.1128/MCB.00906-12. Epub 2012 Sep 10.
10
A novel TBP-TAF complex on RNA polymerase II-transcribed snRNA genes.一种存在于RNA聚合酶II转录的小核RNA基因上的新型TBP-TAF复合物。
Transcription. 2012 Mar-Apr;3(2):92-104. doi: 10.4161/trns.19783. Epub 2012 Mar 1.

本文引用的文献

1
Novel cofactors and TFIIA mediate functional core promoter selectivity by the human TAFII150-containing TFIID complex.新型辅因子和TFIIA通过含人TAFII150的TFIID复合物介导功能性核心启动子选择性。
Mol Cell Biol. 1998 Nov;18(11):6571-83. doi: 10.1128/MCB.18.11.6571.
2
SNAP19 mediates the assembly of a functional core promoter complex (SNAPc) shared by RNA polymerases II and III.SNAP19介导RNA聚合酶II和III共享的功能性核心启动子复合物(SNAPc)的组装。
Genes Dev. 1998 Sep 1;12(17):2664-72. doi: 10.1101/gad.12.17.2664.
3
Promoter-proximal stalling results from the inability to recruit transcription factor IIH to the transcription complex and is a regulated event.启动子近端停滞是由于无法将转录因子IIH招募到转录复合物中所致,是一个受调控的事件。
Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):9767-72. doi: 10.1073/pnas.95.17.9767.
4
The mechanism of transcriptional synergy of an in vitro assembled interferon-beta enhanceosome.体外组装的干扰素-β增强体的转录协同作用机制。
Mol Cell. 1997 Dec;1(1):119-29. doi: 10.1016/s1097-2765(00)80013-1.
5
DA-complex assembly activity required for VP16C transcriptional activation.VP16C转录激活所需的DA复合物组装活性。
Mol Cell Biol. 1998 Jul;18(7):4023-31. doi: 10.1128/MCB.18.7.4023.
6
An interplay between TATA box-binding protein and transcription factors IIE and IIA modulates DNA binding and transcription.TATA 盒结合蛋白与转录因子 IIE 和 IIA 之间的相互作用调节 DNA 结合和转录。
Proc Natl Acad Sci U S A. 1998 Jun 9;95(12):6722-7. doi: 10.1073/pnas.95.12.6722.
7
Transcription factor IIA derepresses TATA-binding protein (TBP)-associated factor inhibition of TBP-DNA binding.转录因子IIA可解除TATA结合蛋白(TBP)相关因子对TBP-DNA结合的抑制作用。
J Biol Chem. 1998 Jun 5;273(23):14293-300. doi: 10.1074/jbc.273.23.14293.
8
Association of transcription factor IIA with TATA binding protein is required for transcriptional activation of a subset of promoters and cell cycle progression in Saccharomyces cerevisiae.转录因子IIA与TATA结合蛋白的结合对于酿酒酵母中一部分启动子的转录激活及细胞周期进程是必需的。
Mol Cell Biol. 1998 May;18(5):2559-70. doi: 10.1128/MCB.18.5.2559.
9
Cloning and biochemical characterization of TAF-172, a human homolog of yeast Mot1.酵母Mot1的人类同源物TAF-172的克隆与生化特性分析
Mol Cell Biol. 1998 Mar;18(3):1701-10. doi: 10.1128/MCB.18.3.1701.
10
The yeast TAF145 inhibitory domain and TFIIA competitively bind to TATA-binding protein.酵母TAF145抑制结构域和TFIIA竞争性结合TATA结合蛋白。
Mol Cell Biol. 1998 Feb;18(2):1003-12. doi: 10.1128/MCB.18.2.1003.