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Major role for mRNA stability in shaping the kinetics of gene induction
被引:84
作者:

Elkon, Ran
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机构:
Netherlands Canc Inst, Div Gene Regulat, NL-1066 CX Amsterdam, Netherlands Netherlands Canc Inst, Div Gene Regulat, NL-1066 CX Amsterdam, Netherlands

Zlotorynski, Eitan
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h-index: 0
机构:
Netherlands Canc Inst, Div Gene Regulat, NL-1066 CX Amsterdam, Netherlands Netherlands Canc Inst, Div Gene Regulat, NL-1066 CX Amsterdam, Netherlands

Zeller, Karen I.
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机构:
Johns Hopkins Sch Med, Div Hematol, Dept Med, Baltimore, MD USA Netherlands Canc Inst, Div Gene Regulat, NL-1066 CX Amsterdam, Netherlands

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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.
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