4.8 Article

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

期刊

CELL
卷 153, 期 5, 页码 1000-1011

出版社

CELL PRESS
DOI: 10.1016/j.cell.2013.05.012

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资金

  1. Israel Science Foundation [1283/07]
  2. Ministry of Health, and Rappaport Foundation [ANR JC 0118-01]
  3. la Ligue
  4. Spanish MCINN
  5. European Union ERDF [BFU2010-21975-C03-01, BFU2010-21975-C03-02]
  6. Regional Valencian Government [GV PROMETEO/2011/088]
  7. Junta de Andalucia [P07-CVI02623, P08-CVI-03508]
  8. MICINN GV
  9. EU
  10. DARPA [D12AP00004]
  11. Center for Excellence in Genome Science from the NHGRI [1P50HG006193]
  12. Gruss-Lipper family postdoctoral fellowship
  13. GV
  14. FPU MICINN

向作者/读者索取更多资源

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.

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