Major role for mRNA stability in shaping the kinetics of gene induction

被引:84
作者
Elkon, Ran [1 ]
Zlotorynski, Eitan [1 ]
Zeller, Karen I. [2 ]
Agami, Reuven [1 ]
机构
[1] Netherlands Canc Inst, Div Gene Regulat, NL-1066 CX Amsterdam, Netherlands
[2] Johns Hopkins Sch Med, Div Hematol, Dept Med, Baltimore, MD USA
来源
BMC GENOMICS | 2010年 / 11卷
关键词
DECAY-RATES; TRANSCRIPTION; EXPRESSION; TRANSIENT; STRESS;
D O I
10.1186/1471-2164-11-259
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: mRNA levels in cells are determined by the relative rates of RNA production and degradation. Yet, to date, most analyses of gene expression profiles were focused on mechanisms which regulate transcription, while the role of mRNA stability in modulating transcriptional networks was to a large extent overlooked. In particular, kinetic waves in transcriptional responses are usually interpreted as resulting from sequential activation of transcription factors. Results: In this study, we examined on a global scale the role of mRNA stability in shaping the kinetics of gene response. Analyzing numerous expression datasets we revealed a striking global anti-correlation between rapidity of induction and mRNA stability, fitting the prediction of a kinetic mathematical model. In contrast, the relationship between kinetics and stability was less significant when gene suppression was analyzed. Frequently, mRNAs that are stable under standard conditions were very rapidly down-regulated following stimulation. Such effect cannot be explained even by a complete shut-off of transcription, and therefore indicates intense modulation of RNA stability. Conclusion: Taken together, our results demonstrate the key role of mRNA stability in determining induction kinetics in mammalian transcriptional networks.
引用
收藏
页数:8
相关论文
共 22 条
[1]   Ranked prediction of p53 targets using hidden variable dynamic modeling [J].
Barenco, M ;
Tomescu, D ;
Brewer, D ;
Callard, R ;
Stark, J ;
Hubank, M .
GENOME BIOLOGY, 2006, 7 (03)
[2]   Transcriptional regulatory cascades in development: Initial rates, not steady state, determine network kinetics [J].
Bolouri, H ;
Davidson, EH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (16) :9371-9376
[3]   Control of gene expression during T cell activation: alternate regulation of mRNA transcription and mRNA stability [J].
Cheadle, C ;
Fan, JS ;
Cho-Chung, YS ;
Werner, T ;
Ray, J ;
Do, L ;
Gorospe, M ;
Becker, KG .
BMC GENOMICS, 2005, 6 (1)
[4]   High-resolution gene expression profiling for simultaneous kinetic parameter analysis of RNA synthesis and decay [J].
Doelken, Lars ;
Ruzsics, Zsolt ;
Raedle, Bernd ;
Friedel, Caroline C. ;
Zimmer, Ralf ;
Mages, Joerg ;
Hoffmann, Reinhard ;
Dickinson, Paul ;
Forster, Thorsten ;
Ghazal, Peter ;
Koszinowski, Ulrich H. .
RNA, 2008, 14 (09) :1959-1972
[5]   Functional genomic delineation of TLR-induced transcriptional networks [J].
Elkon, Ran ;
Linhart, Chaim ;
Halperin, Yonit ;
Shiloh, Yosef ;
Shamir, Ron .
BMC GENOMICS, 2007, 8 (1)
[6]   Conserved principles of mammalian transcriptional regulation revealed by RNA half-life [J].
Friedel, Caroline C. ;
Doelken, Lars ;
Ruzsics, Zsolt ;
Koszinowski, Ulrich H. ;
Zimmer, Ralf .
NUCLEIC ACIDS RESEARCH, 2009, 37 (17) :e115-e115
[7]   Genomic run-on evaluates transcription rates for all yeast genes and identifies gene regulatory mechanisms [J].
García-Martínez, J ;
Aranda, A ;
Pérez-Ortín, JE .
MOLECULAR CELL, 2004, 15 (02) :303-313
[8]   BioMart Central Portal-unified access to biological data [J].
Haider, Syed ;
Ballester, Benoit ;
Smedley, Damian ;
Zhang, Junjun ;
Rice, Peter ;
Kasprzyk, Arek .
NUCLEIC ACIDS RESEARCH, 2009, 37 :W23-W27
[9]   The stability of mRNA influences the temporal order of the induction of genes encoding inflammatory molecules [J].
Hao, Shengli ;
Baltimore, David .
NATURE IMMUNOLOGY, 2009, 10 (03) :281-288
[10]   Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources [J].
Huang, Da Wei ;
Sherman, Brad T. ;
Lempicki, Richard A. .
NATURE PROTOCOLS, 2009, 4 (01) :44-57