Impaired spermatogenesis and male fertility defects in CIZ/Nmp4-disrupted mice

Genes Cells. 2004 Jun;9(6):575-89. doi: 10.1111/j.1356-9597.2004.00746.x.

Abstract

CIZ (Cas interacting zinc finger protein), also called Nmp4 (nuclear matrix protein 4), is a nucleo-cytoplasmic shuttling transcription factor that regulates the expression of collagen and matrix metalloproteinases. CIZ/Nmp4 was originally cloned by its binding to p130(Cas), a focal adhesion protein, and was recently shown to suppress BMP2 (bone mophogenetic protein 2) signalling. To explore the physiological role of CIZ/Nmp4, we disrupted CIZ/Nmp4-gene by inserting beta-galactosidase and neomycin resistance genes into the 2nd exon of CIZ/Nmp4-gene, which is utilized by all the sequenced alternative forms. CIZ-/- mice were born and grew to adulthood. Although they tend to be smaller than wild-type mice, no pathological abnormality was observed except in the testis. Histological analysis of the testes revealed variable degrees of spermatogenic cell degeneration within the seminiferous tubules of CIZ-/- mice, resembling the histology of the 'Germinal-cell aplasia with focal spermatogenesis'. Some of the CIZ-/- male mice developed infertility. TUNEL assay on testis sections revealed an increased occurrence of apoptosis of spermatogenic cells in the testes of CIZ-/- mice. CIZ/Nmp4 was co-localized with Smad1 in the testis, suggesting that a disregulation of BMP signalling could cause these phenotypes. These results suggest that CIZ/Nmp4 plays roles in the progress and the maintenance of spermatogenesis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging
  • Alleles
  • Animals
  • Body Size / genetics
  • Cells, Cultured
  • DNA-Binding Proteins / metabolism
  • Drug Resistance / genetics
  • Exons
  • Gene Expression
  • Genome
  • Infertility, Male / pathology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Neomycin
  • Nuclear Matrix-Associated Proteins / metabolism
  • Nuclear Matrix-Associated Proteins / physiology*
  • Precipitin Tests
  • Smad Proteins
  • Smad1 Protein
  • Spermatogenesis*
  • Stem Cells / cytology
  • Testis / pathology
  • Trans-Activators / metabolism
  • Trans-Activators / physiology*
  • Transcription Factors / metabolism
  • Transcription Factors / physiology*
  • Zinc Fingers / physiology*
  • beta-Galactosidase

Substances

  • DNA-Binding Proteins
  • Nuclear Matrix-Associated Proteins
  • Smad Proteins
  • Smad1 Protein
  • Smad1 protein, mouse
  • Trans-Activators
  • Transcription Factors
  • Zfp384 protein, mouse
  • beta-Galactosidase
  • Neomycin