4.8 Article

Gene-Specific Translation Regulation Mediated by the Hormone-Signaling Molecule EIN2

期刊

CELL
卷 163, 期 3, 页码 684-697

出版社

CELL PRESS
DOI: 10.1016/j.cell.2015.09.036

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资金

  1. NSF [MCB 1158181, 0519869, MCB 0923727, IOS 1444561]
  2. NCSU-RISF
  3. Marie Curie COFUND U-Mobility postdoctoral fellowship
  4. University of Malaga
  5. EU [246550]
  6. Ministerio de Educacion
  7. NSF-REU [MCB 06103224]
  8. NCBI SRA [SRP056795]
  9. Direct For Biological Sciences
  10. Division Of Integrative Organismal Systems [1444561] Funding Source: National Science Foundation
  11. Direct For Biological Sciences
  12. Division Of Integrative Organismal Systems [1254423] Funding Source: National Science Foundation
  13. Direct For Biological Sciences
  14. Div Of Molecular and Cellular Bioscience [1158181, 0519869] Funding Source: National Science Foundation

向作者/读者索取更多资源

The central role of translation in modulating gene activity has long been recognized, yet the systematic exploration of quantitative changes in translation at a genome-wide scale in response to a specific stimulus has only recently become technically feasible. Using the well-characterized signaling pathway of the phytohormone ethylene and plant-optimized genome-wide ribosome footprinting, we have uncovered a molecular mechanism linking this hormone's perception to the activation of a gene-specific translational control mechanism. Characterization of one of the targets of this translation regulatory machinery, the ethylene signaling component EBF2, indicates that the signaling molecule EIN2 and the nonsense-mediated decay proteins UPFs play a central role in this ethylene-induced translational response. Furthermore, the 3'UTR of EBF2 is sufficient to confer translational regulation and required for the proper activation of ethylene responses. These findings represent a mechanistic paradigm of gene-specific regulation of translation in response to a key growth regulator.

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