Primary spermatocyte-specific Cre recombinase activity in transgenic mice

被引:18
作者
Chung, SSW
Cuzin, F
Rassoulzadegan, M
Wolgemuth, DJ
机构
[1] Columbia Univ, Med Ctr, Dept Genet & Dev, New York, NY 10032 USA
[2] Columbia Univ, Med Ctr, Dept Obstet & Gynecol, New York, NY 10032 USA
[3] Columbia Univ, Med Ctr, Ctr Reprod Sci, New York, NY 10032 USA
[4] Columbia Univ, Med Ctr, Inst Human Nutr, New York, NY 10032 USA
[5] Columbia Univ, Med Ctr, Herbert Irving Comprehens Canc Ctr, New York, NY 10032 USA
[6] Univ Nice, INSERM, U470, Nice, France
关键词
Cre recombinase; Sycp1Cre; ROSA26; primary spermatocytes;
D O I
10.1023/B:TRAG.0000034716.73957.f7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:289 / 294
页数:6
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