TATA-binding Protein and Transcription Factor IIB Induce Transcript Slipping during Early Transcription by RNA Polymerase II

被引:11
作者
Gilman, Benjamin [1 ]
Drullinger, Linda F. [1 ]
Kugel, Jennifer F. [1 ]
Goodrich, James A. [1 ]
机构
[1] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
基金
美国国家科学基金会;
关键词
MAJOR LATE PROMOTER; ABORTIVE INITIATION; DNA; ELONGATION; COMPLEXES; ESCAPE; ATP; CLEARANCE; STEPS; TFIIB;
D O I
10.1074/jbc.M900019200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
To better understand the mechanism of steps in early transcription by RNA polymerase II (pol II), we investigated the molecular determinants of transcript slipping within complexes assembled on promoters containing a pre-melted transcription bubble from -9 to +3. Transcript slippage occurs when an RNA transcript contains a repetitive sequence that allows the transcript to slip back and pair with the template strand of the DNA at a new register before transcription continues. We established the contributions of individual transcription factors, DNA elements, and RNA length to slipping on a heteroduplex template using a highly purified human pol II transcription system. We found that transcripts slip at a very defined point in the transcription reaction, after pol II completes phosphodiester bond synthesis at register +5. This point is set by the position of the polymerase active site on the DNA template, as opposed to the length of the transcript, as well as by a repetitive CUCU sequence that must occur from +2 to +5. Interestingly, slipping at this juncture is induced by TATA-binding protein and transcription factor IIB and requires a TATA box but not a transcription factor IIB recognition sequence. We propose a model in which transcribing complexes, upon completing phosphodiester bond synthesis at register +5, enter one of two branches in which they either complete productive synthesis of the transcript or undergo multiple rounds of transcript slipping.
引用
收藏
页码:9093 / 9098
页数:6
相关论文
共 26 条
[1]
TFIIB and the regulation of transcription by RNA polymerase II [J].
Deng, Wensheng ;
Roberts, Stefan G. E. .
CHROMOSOMA, 2007, 116 (05) :417-429
[2]
Promoter escape by RNA polymerase II [J].
Dvir, A .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2002, 1577 (02) :208-223
[3]
TRANSCRIPTION FACTORS IIE AND IIH AND ATP HYDROLYSIS DIRECT PROMOTER CLEARANCE BY RNA-POLYMERASE-II [J].
GOODRICH, JA ;
TJIAN, R .
CELL, 1994, 77 (01) :145-156
[4]
An 8 nt RNA triggers a rate-limiting shift of RNA polymerase II complexes into elongation [J].
Hieb, Aaron R. ;
Baran, Sean ;
Goodrich, James A. ;
Kugel, Jennifer F. .
EMBO JOURNAL, 2006, 25 (13) :3100-3109
[5]
Three transitions in the RNA polymerase II transcription complex during initiation [J].
Holstege, FCP ;
Fiedler, U ;
Timmers, HTM .
EMBO JOURNAL, 1997, 16 (24) :7468-7480
[6]
Opening of an RNA polymerase II promoter occurs in two distinct steps and requires the basal transcription factors IIE and IIH [J].
Holstege, FCP ;
vanderVliet, PC ;
Timmers, HTM .
EMBO JOURNAL, 1996, 15 (07) :1666-1677
[7]
JACOB GA, 1991, J BIOL CHEM, V266, P22537
[8]
Initially transcribed sequences strongly affect the extent of abortive initiation by RNA polymerase II [J].
Keene, RG ;
Luse, DS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (17) :11526-11534
[9]
Mechanism of ATP-dependent promoter melting by transcription factor IIH [J].
Kim, TK ;
Ebright, RH ;
Reinberg, D .
SCIENCE, 2000, 288 (5470) :1418-1421
[10]
The 8-nucleotide-long RNA:DNA hybrid is a primary stability determinant of the RNA polymerase II elongation complex [J].
Kireeva, ML ;
Komissarova, N ;
Waugh, DS ;
Kashlev, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (09) :6530-6536