MFN2 interacts with nuage-associated proteins and is essential for male germ cell development by controlling mRNA fate during spermatogenesis

Development. 2021 Apr 1;148(7):dev196295. doi: 10.1242/dev.196295. Epub 2021 Apr 15.

Abstract

Mitochondria play a crucial role in spermatogenesis and are regulated by several mitochondrial fusion proteins. However, their functional importance associated with their structure formation and mRNA fate regulation during spermatogenesis remains unclear. Here, we show that mitofusin 2 (MFN2), a mitochondrial fusion protein, interacts with nuage-associated proteins (including MIWI, DDX4, TDRKH and GASZ) in mice. Conditional mutation of Mfn2 in postnatal germ cells results in male sterility due to germ cell developmental defects. Moreover, MFN2 interacts with MFN1, another mitochondrial fusion protein with a high-sequence similarity to MFN2, in testes to facilitate spermatogenesis. Simultaneous mutation of Mfn1 and Mfn2 in testes causes very severe infertile phenotypes. Importantly, we show that MFN2 is enriched in polysome fractions of testes and interacts with MSY2, a germ cell-specific DNA/RNA-binding protein, to control gamete-specific mRNA (such as Spata19) translational activity during spermatogenesis. Collectively, our findings demonstrate that MFN2 interacts with nuage-associated proteins and MSY2 to regulate male germ cell development by controlling several gamete-specific mRNA fates.

Keywords: MSY2; Mice; Mitofusins; Nuage proteins; Spermatogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Argonaute Proteins
  • Cell Differentiation / physiology*
  • DEAD-box RNA Helicases
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Fertility
  • GTP Phosphohydrolases / genetics*
  • GTP Phosphohydrolases / metabolism*
  • Gene Expression Regulation, Developmental
  • Gene Knockout Techniques
  • Germ Cells / metabolism*
  • Germ Cells / pathology
  • HEK293 Cells
  • Humans
  • Infertility, Male / genetics
  • Male
  • Membrane Proteins / metabolism
  • Mice
  • Mitochondria / metabolism
  • Mitochondrial Dynamics
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism
  • Mutation
  • RNA, Messenger / metabolism*
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism
  • Spermatogenesis / genetics*
  • Spermatogenesis / physiology*
  • Testis / metabolism
  • Testis / pathology

Substances

  • Argonaute Proteins
  • DNA-Binding Proteins
  • Membrane Proteins
  • Mitochondrial Proteins
  • Piwil1 protein, mouse
  • RNA, Messenger
  • RNA-Binding Proteins
  • Tdrkh protein, mouse
  • Ddx4 protein, mouse
  • GTP Phosphohydrolases
  • MFN2 protein, human
  • Mfn1 protein, mouse
  • Mfn2 protein, mouse
  • DEAD-box RNA Helicases