Capping, splicing, and 3′ processing are independently stimulated by RNA polymerase II:: different functions for different segments of the CTD

被引:184
作者
Fong, N [1 ]
Bentley, DL [1 ]
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Mol Genet & Biochem, Denver, CO 80262 USA
关键词
mRNA processing; RNA polymerase II; CstF; carboxy-terminal domain; splicing;
D O I
10.1101/gad.889101
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Capping, splicing, and cleavage/polyadenylation of pre-mRNAs are interdependent events that are all stimulated in vivo by the carboxy-terminal domain (CTD) of RNA Pol II. We show that the CTD independently enhances splicing and 3 ' processing and that stimulation of splicing by enhancers is facilitated by the CTD. We provide evidence that stimulation of 3 ' processing by the CTD requires contact with the 50-kD subunit of the cleavage stimulation factor, CstF. Overexpression of the CTD-binding domain of CstF p50 had a dominant-negative effect on 3 ' processing without disrupting the CstF complex. The CTD comprises 52 heptad repeats. The CTD carboxyl terminus including heptads 27-52 supported capping, splicing, and 3 ' processing but the amino terminus supported only capping. We conclude that the CTD independently stimulates ail three major pre-mRNA processing steps and that different regions of the CTD can serve distinct functions in pre-mRNA processing.
引用
收藏
页码:1783 / 1795
页数:13
相关论文
共 58 条
[1]   Cleavage/polyadenylation factor IA associates with the carboxyl-terminal domain of RNA polymerase II in Saccharomyces cerevisiae [J].
Barillà, D ;
Lee, BA ;
Proudfoot, NJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (02) :445-450
[2]   GENETIC-ANALYSIS OF THE REPETITIVE CARBOXYL-TERMINAL DOMAIN OF THE LARGEST SUBUNIT OF MOUSE RNA POLYMERASE-II [J].
BARTOLOMEI, MS ;
HALDEN, NF ;
CULLEN, CR ;
CORDEN, JL .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (01) :330-339
[3]   Transcriptional termination in the Balbiani ring 1 gene is closely coupled to 3′-end formation and excision of the 3′-terminal intron [J].
Baurén, G ;
Belikov, S ;
Wieslander, L .
GENES & DEVELOPMENT, 1998, 12 (17) :2759-2769
[4]   Coupling RNA polymerase II transcription with pre-mRNA processing [J].
Bentley, D .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (03) :347-351
[5]   SPLICE SITE SELECTION, RATE OF SPLICING, AND ALTERNATIVE SPLICING ON NASCENT TRANSCRIPTS [J].
BEYER, AL ;
OSHEIM, YN .
GENES & DEVELOPMENT, 1988, 2 (06) :754-765
[6]   Exonic splicing enhancers: mechanism of action, diversity and role in human genetic diseases [J].
Blencowe, BJ .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (03) :106-110
[7]   mRNA capping enzyme is recruited to the transcription complex by phosphorylation of the RNA polymerase II carboxy-terminal domain [J].
Cho, EJ ;
Takagi, T ;
Moore, CR ;
Buratowski, S .
GENES & DEVELOPMENT, 1997, 11 (24) :3319-3326
[8]  
Cooke C, 1996, MOL CELL BIOL, V16, P2579
[9]   PROMOTER-PROXIMAL PAUSING BY RNA POLYMERASE-II INVITRO - TRANSCRIPTS SHORTER THAN 20 NUCLEOTIDES ARE NOT CAPPED [J].
COPPOLA, JA ;
FIELD, AS ;
LUSE, DS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (05) :1251-1255
[10]   Identification of a new class of exonic splicing enhancers by in vivo selection [J].
Coulter, LR ;
Landree, MA ;
Cooper, TA .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (04) :2143-2150