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TTC5 mediates autoregulation of tubulin via mRNA degradation.

Zhewang LinIvana GasicViswanathan ChandrasekaranNiklas PetersSichen ShaoTimothy J MitchisonRamanujan S Hegde
Published in: Science (New York, N.Y.) (2019)
Tubulins play crucial roles in cell division, intracellular traffic, and cell shape. Tubulin concentration is autoregulated by feedback control of messenger RNA (mRNA) degradation via an unknown mechanism. We identified tetratricopeptide protein 5 (TTC5) as a tubulin-specific ribosome-associating factor that triggers cotranslational degradation of tubulin mRNAs in response to excess soluble tubulin. Structural analysis revealed that TTC5 binds near the ribosome exit tunnel and engages the amino terminus of nascent tubulins. TTC5 mutants incapable of ribosome or nascent tubulin interaction abolished tubulin autoregulation and showed chromosome segregation defects during mitosis. Our findings show how a subset of mRNAs can be targeted for coordinated degradation by a specificity factor that recognizes the nascent polypeptides they encode.
Keyphrases
  • single cell
  • cell therapy
  • binding protein
  • gene expression
  • stem cells
  • drug delivery
  • mesenchymal stem cells
  • reactive oxygen species
  • amino acid
  • genome wide
  • cerebral blood flow