Primary spermatocyte-specific Cre recombinase activity in transgenic mice

Transgenic Res. 2004 Jun;13(3):289-94. doi: 10.1023/b:trag.0000034716.73957.f7.

Abstract

We have evaluated the specificity of Cre recombinase activity in transgenic mice expressing Cre under the control of the synatonemal complex protein 1 (Sycp1) gene promoter. Sycp1Cre mice were crossed with the ROSA26 reporter line R26R, to monitor the male germ cell stage-specificity of Cre activity as well as to verify that Cre was not active previously during development of other tissues. X-gal staining detected Cre-mediated recombination only in testis. Detailed histological examination indicated that weak Cre-mediated recombination occurred as early as in zygotene spermatocytes at stage XI of the cycle of the seminiferous epithelium. Robust expression of X-gal was detected in early to mid-late spermatocytes at stages V-VIII. We conclude that this transgenic line is a powerful tool for deleting genes of interest specifically during male meiosis.

Publication types

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

MeSH terms

  • Animals
  • Crosses, Genetic
  • DNA-Binding Proteins
  • Galactosides
  • Gene Expression*
  • Histological Techniques
  • Indoles
  • Integrases / metabolism*
  • Male
  • Mice / metabolism*
  • Mice, Transgenic
  • Nuclear Proteins / genetics
  • Promoter Regions, Genetic / genetics
  • Spermatocytes / cytology
  • Spermatocytes / enzymology*
  • Testis / metabolism

Substances

  • DNA-Binding Proteins
  • Galactosides
  • Indoles
  • Nuclear Proteins
  • Sycp1 protein, mouse
  • Cre recombinase
  • Integrases
  • 5-bromo-4-chloro-3-indolyl beta-galactoside