Differential expression of multiple alternative spliceforms of the Men1 tumor suppressor gene in mouse

Int J Mol Med. 2001 Dec;8(6):681-9.


The multiple endocrine neoplasia type 1 gene (MEN1) is a tumor suppressor gene associated with the development of tumors in the parathyroids, the pituitary, and the pancreas and has also been linked to impaired germ cell production. The murine ortholog, Men1, is highly homologous to the human counterpart both at DNA and protein levels. The present study was undertaken to further approach the function of Men1 and its encoded protein menin. By 5' RACE and RT-PCR four alternative splice variants were identified, indicating a 5' heterogeneity of Men1 similar to the human counterpart. By mRNA in situ hybridization of embryonal and adult mouse tissues, all four splice variants were shown to be expressed, albeit at varying timepoints and levels in the different tissues. However, a putative isoform postulated from the DNA sequence, which would elongate the reading frame by 15 bases at the exon 2/intron 2 junction, was not found to occur in mouse. The strongest expression was detected in testis, both at the mRNA and protein level and was therefore further characterized by protein analysis of cells isolated from different stages of the spermatogenesis. Western blotting revealed a single protein of approximately 70 kDa detected in total testis, isolated pachytene spermatocytes and in haploid spermatids. Notably, no menin expression was detectable in the extracts from epididymis where the maturation of sperms is almost completed, suggesting that menin plays a crucial role during spermatogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing*
  • Animals
  • Blotting, Northern
  • Blotting, Western
  • Embryo, Mammalian / metabolism
  • Female
  • Gene Expression Regulation
  • Gene Expression Regulation, Developmental
  • Genes, Tumor Suppressor
  • In Situ Hybridization
  • Male
  • Mice
  • Mice, Inbred Strains
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / metabolism
  • Pregnancy
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Proto-Oncogene Proteins*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Spermatogenesis / genetics
  • Tissue Distribution


  • MEN1 protein, human
  • Neoplasm Proteins
  • Protein Isoforms
  • Proto-Oncogene Proteins
  • RNA, Messenger