Interaction between NANOS2 and the CCR4-NOT deadenylation complex is essential for male germ cell development in mouse

PLoS One. 2012;7(3):e33558. doi: 10.1371/journal.pone.0033558. Epub 2012 Mar 20.

Abstract

Nanos is one of the evolutionarily conserved proteins implicated in germ cell development and we have previously shown that it interacts with the CCR4-NOT deadenylation complex leading to the suppression of specific RNAs. However, the molecular mechanism and physiological significance of this interaction have remained elusive. In our present study, we identify CNOT1, a component of the CCR4-NOT deadenylation complex, as a direct factor mediating the interaction with NANOS2. We find that the first 10 amino acids (AAs) of NANOS2 are required for this binding. We further observe that a NANOS2 mutant lacking these first 10 AAs (NANOS2-ΔN10) fails to rescue defects in the Nanos2-null mouse. Our current data thus indicate that the interaction with the CCR4-NOT deadenylation complex is essential for NANOS2 function. In addition, we further demonstrate that NANOS2-ΔN10 can associate with specific mRNAs as well as wild-type NANOS2, suggesting the existence of other NANOS2-associated factor(s) that determine the specificity of RNA-binding independently of the CCR4-NOT deadenylation complex.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism
  • Blotting, Western
  • Carrier Proteins / physiology*
  • Embryo, Mammalian / cytology
  • Embryo, Mammalian / metabolism*
  • Gene Expression Profiling
  • HeLa Cells
  • Humans
  • Immunoprecipitation
  • Male
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Oligonucleotide Array Sequence Analysis
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism*
  • RNA-Binding Proteins
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Ribonucleases / genetics
  • Ribonucleases / metabolism*
  • Spermatozoa / growth & development*
  • Spermatozoa / metabolism*
  • Testis / embryology
  • Testis / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transgenes / physiology

Substances

  • Biomarkers, Tumor
  • CNOT1 protein, human
  • Carrier Proteins
  • Nanos2 protein, mouse
  • RNA, Messenger
  • RNA-Binding Proteins
  • Transcription Factors
  • Ribonucleases
  • mRNA deadenylase