4.8 Article

Translational Homeostasis via the mRNA Cap-Binding Protein, elF4E

Journal

MOLECULAR CELL
Volume 46, Issue 6, Pages 847-858

Publisher

CELL PRESS
DOI: 10.1016/j.molcel.2012.04.004

Keywords

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Funding

  1. Japan Society for the Promotion of Science (JSPS)
  2. Fondation pour la Recherche Medicate
  3. Canadian Institutes of Health Research (CIHR) [MOP 7214]
  4. NCI [CA51995]

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Translational control of gene expression plays a key role in many biological processes. Consequently, the activity of the translation apparatus is under tight homeostatic control. elF4E, the mRNA 5' cap-binding protein, facilitates cap-dependent translation and is a major target for translational control. elF4E activity is controlled by a family of repressor proteins, termed 4E-binding proteins (4E-BPs). Here, we describe the surprising finding that despite the importance of elF4E for translation, a drastic knockdown of elF4E caused only minor reduction in translation. This conundrum can be explained by the finding that 4E-BP1 is degraded in elF4E-knock-down cells. Hypophosphorylated 4E-BP1, which binds to elF4E, is degraded, whereas hyperphosphorylated 4E-BP1 is refractory to degradation. We identified the KLHL25-CUL3 complex as the E3 ubiquitin ligase, which targets hypophosphorylated 4E-BP1. Thus, the activity of elF4E is under homeostatic control via the regulation of the levels of its repressor protein 4E-BP1 through ubiquitination.

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