Crosstalk between mRNA 3′ End Processing and Transcription Initiation

被引:127
作者
Mapendano, Christophe K. [1 ,2 ]
Lykke-Andersen, Soren [1 ,2 ]
Kjems, Jorgen [2 ]
Bertrand, Edouard [3 ]
Jensen, Torben Heick [1 ,2 ]
机构
[1] Aarhus Univ, Ctr mRNP Biogenesis & Metab, DK-8000 Aarhus, Denmark
[2] Aarhus Univ, Dept Mol Biol, DK-8000 Aarhus, Denmark
[3] CNRS, Inst Mol Genet Montpellier, UMR 5535, F-34293 Montpellier, France
基金
新加坡国家研究基金会;
关键词
POLYMERASE-II TRANSCRIPTION; GENE LOOPS; IN-VIVO; EXONUCLEASE XRN2; HUMAN-CELLS; P-TEFB; TERMINATION; ELONGATION; CLEAVAGE; SITES;
D O I
10.1016/j.molcel.2010.10.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transcription and mRNA maturation are interdependent events. Although stimulatory connections between these processes within the same round of transcription are well described, functional coupling between separate transcription cycles remains elusive. Comparing time-resolved transcription profiles of single-copy integrated beta-globin gene variants, we demonstrate that a polyadenylation site mutation decreases transcription initiation of the same gene. Upon depletion of the 3' end processing and transcription termination factor PCF11, endogenous genes exhibit a similar phenotype. Readthrough RNA polymerase II (RNAPII) engaged on polyadenylation site-mutated transcription units sequester the transcription initiation/elongation factors TBP, TFIIB and CDK9, leading to their depletion at the promoter. Additionally, high levels of TBP and TFIIB appear inside the gene body, and Ser2-phosphorylated RNAPII accumulates at the promoter. Our data demonstrate that 3' end formation stimulates transcription initiation and suggest that coordinated recycling of factors from a gene terminator back to the promoter is essential for sustaining continued transcription.
引用
收藏
页码:410 / 422
页数:13
相关论文
共 41 条
[1]   Ctk1 promotes dissociation of basal transcription factors from elongating RNA polymerase II [J].
Ahn, Seong Hoon ;
Keogh, Michael-Christopher ;
Buratowski, Stephen .
EMBO JOURNAL, 2009, 28 (03) :205-212
[2]   Phosphorylation of serine 2 within the RNA polymerase IIC-terminal domain couples transcription and 3′ end processing [J].
Ahn, SH ;
Kim, M ;
Buratowski, S .
MOLECULAR CELL, 2004, 13 (01) :67-76
[3]   A role for the CPF 3′-end processing machinery in RNAP II-dependent gene looping [J].
Ansari, A ;
Hampsey, M .
GENES & DEVELOPMENT, 2005, 19 (24) :2969-2978
[4]   Ribozyme cleavage reveals connections between mRNA release from the site of transcription and pre-mRNA processing [J].
Bird, G ;
Fong, N ;
Gatlin, JC ;
Farabaugh, S ;
Bentley, DL .
MOLECULAR CELL, 2005, 20 (05) :747-758
[5]   INTRONS INCREASE TRANSCRIPTIONAL EFFICIENCY IN TRANSGENIC MICE [J].
BRINSTER, RL ;
ALLEN, JM ;
BEHRINGER, RR ;
GELINAS, RE ;
PALMITER, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (03) :836-840
[6]   Progression through the RNA Polymerase II CTD Cycle [J].
Buratowski, Stephen .
MOLECULAR CELL, 2009, 36 (04) :541-546
[7]   Flavopiridol inactivates P-TEFb and blocks most RNA polymerase II transcription in vivo [J].
Chao, SH ;
Price, DH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (34) :31793-31799
[8]   A 5′ splice site enhances the recruitment of basal transcription initiation factors in vivo [J].
Damgaard, Christian Kroun ;
Kahns, Soren ;
Lykke-Andersen, Soren ;
Nielsen, Anders Lade ;
Jensen, Torben Heick ;
Kjems, Jorgen .
MOLECULAR CELL, 2008, 29 (02) :271-278
[9]   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
[10]   In vivo dynamics of RNA polymerase II transcription [J].
Darzacq, Xavier ;
Shav-Tal, Yaron ;
de Turris, Valeria ;
Brody, Yehuda ;
Shenoy, Shailesh M. ;
Phair, Robert D. ;
Singer, Robert H. .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2007, 14 (09) :796-806