Gene Expression Is Circular: Factors for mRNA Degradation Also Foster mRNA Synthesis

被引:263
作者
Haimovich, Gal [1 ]
Medina, Daniel A. [2 ,3 ]
Causse, Sebastien Z. [4 ]
Garber, Manuel [5 ]
Millan-Zambrano, Gonzalo [6 ]
Barkai, Oren [1 ]
Chavez, Sebastian [6 ]
Perez-Ortin, Jose E. [2 ,3 ]
Darzacq, Xavier [4 ]
Choder, Mordechai [1 ]
机构
[1] Technion Israel Inst Technol, Rappaport Fac Med, Dept Mol Microbiol, IL-31096 Haifa, Israel
[2] Univ Valencia, Dept Bioquim & Biol Mol, Fac Biol, E-46100 Valencia, Spain
[3] Univ Valencia, ERI Biotecmed, E-46100 Valencia, Spain
[4] Ecole Normale Super, CNRS, UMR 8197, IBENS,Inst Biol, F-75005 Paris, France
[5] Univ Massachusetts, Sch Med, Worcester, MA 01655 USA
[6] Univ Seville, Fac Biol, Dept Genet, E-41012 Seville, Spain
基金
以色列科学基金会;
关键词
SACCHAROMYCES-CEREVISIAE; POLYMERASE-II; GENOME-WIDE; IN-VIVO; TRANSCRIPTION ELONGATION; YEAST; DECAY; COMPLEX; TRANSLATION; CYTOPLASM;
D O I
10.1016/j.cell.2013.05.012
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
Maintaining proper mRNA levels is a key aspect in the regulation of gene expression. The balance between mRNA synthesis and decay determines these levels. We demonstrate that most yeast mRNAs are degraded by the cytoplasmic 50-to-30 pathway (the "decaysome''), as proposed previously. Unexpectedly, the level of these mRNAs is highly robust to perturbations in this major pathway because defects in various decaysome components lead to transcription downregulation. Moreover, these components shuttle between the cytoplasm and the nucleus, in a manner dependent on proper mRNA degradation. In the nucleus, they associate with chromatin-preferentially similar to 30 bp upstream of transcription start-sites-and directly stimulate transcription initiation and elongation. The nuclear role of the decaysome in transcription is linked to its cytoplasmic role in mRNA decay; linkage, in turn, seems to depend on proper shuttling of its components. The gene expression process is therefore circular, whereby the hitherto first and last stages are interconnected.
引用
收藏
页码:1000 / 1011
页数:12
相关论文
共 57 条
[1]
Alberola TM, 2004, INT MICROBIOL, V7, P199
[2]
The 3′ to 5′ degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 3′ to 5′ exonucleases of the exosome complex [J].
Anderson, JSJ ;
Parker, R .
EMBO JOURNAL, 1998, 17 (05) :1497-1506
[3]
Targeted mRNA degradation by deadenylation-independent decapping [J].
Badis, G ;
Saveanu, C ;
Fromont-Racine, M ;
Jacquier, A .
MOLECULAR CELL, 2004, 15 (01) :5-15
[4]
A Universal RNA Polymerase II CTD Cycle Is Orchestrated by Complex Interplays between Kinase, Phosphatase, and Isomerase Enzymes along Genes [J].
Bataille, Alain R. ;
Jeronimo, Celia ;
Jacques, Pierre-Etienne ;
Laramee, Louise ;
Fortin, Marie-Eve ;
Forest, Audrey ;
Bergeron, Maxime ;
Hanes, Steven D. ;
Robert, Francois .
MOLECULAR CELL, 2012, 45 (02) :158-170
[5]
Promoter Elements Regulate Cytoplasmic mRNA Decay [J].
Bregman, Almog ;
Avraham-Kelbert, Moran ;
Barkai, Oren ;
Duek, Lea ;
Guterman, Adi ;
Choder, Mordechai .
CELL, 2011, 147 (07) :1473-1483
[6]
Yeast poly(A)-binding protein Pab1 shuttles between the nucleus and the cytoplasm and functions in mRNA export [J].
Brune, C ;
Munchel, SE ;
Fischer, N ;
Podtelejnikov, AV ;
Weis, K .
RNA, 2005, 11 (04) :517-531
[7]
A chromatin-mediated mechanism for specification of conditional transcription factor targets [J].
Buck, Michael J. ;
Lieb, Jason D. .
NATURE GENETICS, 2006, 38 (12) :1446-1451
[8]
Structural basis of RNA polymerase II backtracking, arrest and reactivation [J].
Cheung, Alan C. M. ;
Cramer, Patrick .
NATURE, 2011, 471 (7337) :249-253
[9]
Nascent transcript sequencing visualizes transcription at nucleotide resolution [J].
Churchman, L. Stirling ;
Weissman, Jonathan S. .
NATURE, 2011, 469 (7330) :368-+
[10]
Eukaryotic mRNA decapping [J].
Coller, J ;
Parker, R .
ANNUAL REVIEW OF BIOCHEMISTRY, 2004, 73 :861-890