Functional interactions between the transcription and mRNA 3′ end processing machineries mediated by Ssu72 and Sub1

被引:123
作者
He, XY
Khan, AU
Cheng, HL
Pappas, DL
Hampsey, M
Moore, CL [1 ]
机构
[1] Tufts Univ, Sch Med, Dept Mol Biol & Microbiol, Boston, MA 02111 USA
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Biochem, Piscataway, NJ 08854 USA
关键词
RNAP II; transcription initiation; transcription termination; 3 ' end processing; cleavage/polyadenylation;
D O I
10.1101/gad.1075203
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Transcription and processing of pre-mRNA are coupled events. By using a combination of biochemical, molecular, and genetic methods, we have found that the phylogenetically conserved transcription factor Ssu72 is a component of the cleavage/polyadenylation factor (CPF) of Saccharomyces cerevisiae. Our results demonstrate that Ssu72 is required for 3' end cleavage of pre-mRNA but is dispensable for poly(A) addition and RNAP II termination. The in vitro cleavage defect caused by depletion of Ssu72 from cells can be rescued by addition of recombinant Ssu72. Ssu72 interacts physically and genetically with the Pta1 subunit of CPF. Overexpression of PTA1 causes synthetic lethality in an ssu72-3 mutant. Moreover, Sub1, which has been implicated in transcription initiation and termination, also interacts with Pta1, and overexpression of SUB1 suppresses the growth and processing defect of a pta1 mutation. Physical interactions of Ssu72 and Sub1 with Pta1 are mutually exclusive. Based on the interactions of Ssu72 and Sub1 with both the Ptal of CPF and the TFIIB component of the initiation complex, we present a model describing how these novel connections between the transcription and 3' end processing machineries might facilitate transitions in the RNAP II transcription cycle.
引用
收藏
页码:1030 / 1042
页数:13
相关论文
共 54 条
[1]   The mRNA assembly line: transcription and processing machines in the same factory [J].
Bentley, D .
CURRENT OPINION IN CELL BIOLOGY, 2002, 14 (03) :336-342
[2]   Coupling termination of transcription to messenger RNA maturation in yeast [J].
Birse, CE ;
Minvielle-Sebastia, L ;
Lee, BA ;
Keller, W ;
Proudfoot, NJ .
SCIENCE, 1998, 280 (5361) :298-301
[3]   Evolutionarily conserved interaction between CstF-64 and PC4 links transcription, polyadenylation, and termination [J].
Calvo, O ;
Manley, JL .
MOLECULAR CELL, 2001, 7 (05) :1013-1023
[4]   SEPARATION OF FACTORS REQUIRED FOR CLEAVAGE AND POLYADENYLATION OF YEAST PRE-MESSENGER-RNA [J].
CHEN, J ;
MOORE, C .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (08) :3470-3481
[5]   Transcription factor TFIID recruits factor CPSF for formation of 3' end of mRNA [J].
Dantonel, JC ;
Murthy, KGK ;
Manley, JL ;
Tora, L .
NATURE, 1997, 389 (6649) :399-402
[6]   Yhh1p/Cft1p directly links poly(A) site recognition and RNA polymerase II transcription termination [J].
Dichtl, B ;
Blank, D ;
Sadowski, M ;
Hübner, W ;
Weiser, S ;
Keller, W .
EMBO JOURNAL, 2002, 21 (15) :4125-4135
[7]   A role for SSU72 in balancing RNA polymerase II transcription elongation and termination [J].
Dichtl, B ;
Blank, D ;
Ohnacker, M ;
Friedlein, A ;
Roeder, D ;
Langen, H ;
Keller, W .
MOLECULAR CELL, 2002, 10 (05) :1139-1150
[8]   HEAT-INDUCIBLE DEGRON - A METHOD FOR CONSTRUCTING TEMPERATURE-SENSITIVE MUTANTS [J].
DOHMEN, RJ ;
WU, PP ;
VARSHAVSKY, A .
SCIENCE, 1994, 263 (5151) :1273-1276
[9]   T7 RNA polymerase-directed transcripts are processed in yeast and link 3′ end formation to mRNA nuclear export [J].
Dower, K ;
Rosbash, M .
RNA, 2002, 8 (05) :686-697
[10]   A history of poly A sequences: From formation to factors to function [J].
Edmonds, M .
PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, VOL 71, 2002, 71 :285-389