Regulation of L-threonine dehydrogenase in somatic cell reprogramming

Stem Cells. 2013 May;31(5):953-65. doi: 10.1002/stem.1335.

Abstract

Increasing evidence suggests that metabolic remodeling plays an important role in the regulation of somatic cell reprogramming. Threonine catabolism mediated by L-threonine dehydrogenase (TDH) has been recognized as a specific metabolic trait of mouse embryonic stem cells. However, it remains unknown whether TDH-mediated threonine catabolism could regulate reprogramming. Here, we report TDH as a novel regulator of somatic cell reprogramming. Knockdown of TDH inhibits, whereas induction of TDH enhances reprogramming efficiency. Moreover, microRNA-9 post-transcriptionally regulates the expression of TDH and thereby inhibits reprogramming efficiency. Furthermore, protein arginine methyltransferase (PRMT5) interacts with TDH and mediates its post-translational arginine methylation. PRMT5 appears to regulate TDH enzyme activity through both methyltransferase-dependent and -independent mechanisms. Functionally, TDH-facilitated reprogramming efficiency is further enhanced by PRMT5. These results suggest that TDH-mediated threonine catabolism controls somatic cell reprogramming and indicate the importance of post-transcriptional and post-translational regulation of TDH.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohol Oxidoreductases / biosynthesis
  • Alcohol Oxidoreductases / genetics
  • Alcohol Oxidoreductases / metabolism*
  • Animals
  • Arginine / metabolism
  • Cell Differentiation / physiology
  • Cellular Reprogramming / physiology*
  • Gene Expression Regulation, Developmental
  • Induced Pluripotent Stem Cells / cytology*
  • Induced Pluripotent Stem Cells / enzymology
  • Induced Pluripotent Stem Cells / metabolism
  • Induced Pluripotent Stem Cells / physiology
  • Methylation
  • Mice
  • MicroRNAs / genetics
  • Protein Methyltransferases / metabolism
  • Protein-Arginine N-Methyltransferases
  • RNA Interference
  • Stem Cells / cytology*
  • Stem Cells / enzymology
  • Stem Cells / metabolism
  • Stem Cells / physiology
  • Threonine / metabolism*

Substances

  • MIRN9 microRNA, mouse
  • MicroRNAs
  • Threonine
  • Arginine
  • Alcohol Oxidoreductases
  • L-threonine 3-dehydrogenase
  • Protein Methyltransferases
  • Prmt5 protein, mouse
  • Protein-Arginine N-Methyltransferases