Nm23-M5 mediates round and elongated spermatid survival by regulating GPX-5 levels

FEBS Lett. 2009 Apr 17;583(8):1292-8. doi: 10.1016/j.febslet.2009.03.023. Epub 2009 Mar 19.

Abstract

Nucleoside diphosphate (NDP) kinases are involved in numerous regulatory processes associated with proliferation, development, and differentiation. Previously, we cloned a new member of the NDPK family from mouse, Nm23-M5, which encodes a 211-amino acid protein and has 86% identity to the human Nm23-H5 [Hwang, K.C., Ok, D.W., Hong, J.C., Kim, M.O. and Kim, J.H. (2003) Cloning, sequencing, and characterization of the murine Nm23-M5 gene during mouse spermatogenesis and spermiogenesis. Biochem. Biophys. Res. Commun. 306, 198-207]. To better understand Nm23-M5 function, we generated transgenic mice with reduced Nm23-M5 levels in vivo using a short hairpin RNA (shRNA) knock-down system. Nm23-M5 expression was markedly reduced, as indicated by Northern and Western blot analysis. Nm23-M5 shRNA transgenic mice exhibited reduced numbers of haploid cells. Furthermore, the antioxidant enzyme glutathione peroxidase 5 (GPX-5) is regulated by Nm23-M5 at the level of both expression and activity. These results reveal that expression of Nm23-M5 plays a critical role in spermiogenesis by increasing the cellular levels of GPX-5 to eliminate reactive oxygen species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Blotting, Northern
  • Blotting, Western
  • CHO Cells
  • Cell Survival / physiology*
  • Cloning, Molecular
  • Cricetinae
  • Cricetulus
  • DNA Primers
  • Glutathione Peroxidase / metabolism*
  • Male
  • Mice
  • Mice, Transgenic
  • NM23 Nucleoside Diphosphate Kinases / genetics
  • NM23 Nucleoside Diphosphate Kinases / physiology*
  • Reactive Oxygen Species
  • Reverse Transcriptase Polymerase Chain Reaction
  • Spermatids / cytology*
  • Spermatogenesis / genetics

Substances

  • DNA Primers
  • NM23 Nucleoside Diphosphate Kinases
  • Reactive Oxygen Species
  • Glutathione Peroxidase
  • selenium-independent glutathione peroxidase