Azoospermia in mice with targeted disruption of the Brek/Lmtk2 (brain-enriched kinase/lemur tyrosine kinase 2) gene

被引:44
作者
Kawa, Seiji
Ito, Chizuru
Toyama, Yoshiro
Maekawa, Mamiko
Tezuka, Tohru
Nakamura, Takahisa
Nakazawa, Takanobu
Yokoyama, Kazumasa
Yoshida, Nobuaki
Toshimori, Kiyotaka
Yamamoto, Tadashi
机构
[1] Univ Tokyo, Inst Med Sci, Div Oncol, Minato Ku, Tokyo 1088639, Japan
[2] Univ Tokyo, Inst Med Sci, Ctr Med Expt, Lab Gene Express & Regulat, Tokyo 1088639, Japan
[3] Chiba Univ, Grad Sch Med, Dept Anat & Dev Biol, Chiba 2608670, Japan
关键词
AATYK; BREK; infertility; LMTK2; spermatogenesis;
D O I
10.1073/pnas.0603603103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Brek/Lmtk2 (brain-enriched kinase/lemur tyrosine kinase 2) is a member of the Aatyk family of kinases that comprises Aatyk1, Brek/Lmtk2/Aatyk2, and Aatyk3. Although several potential roles have been proposed for Brek and other Aatyk family members, the physiological functions of these kinases remain unclear. Here, we report that Brek(-/-) male mice are infertile, with azoospermia. Detailed histological analysis revealed that Brek(-/-) germ cells differentiated normally until the round-spermatid stage, but failed to undergo the normal change in morphology to become elongated spermatids. Testicular somatic cells appeared normal in these mice. Expression of Brek in testis was restricted to the germ cells, suggesting that the maturations of germ cells in Brek(-/-) mice are affected in a cell-autonomous manner. On the basis of these findings, we concluded that Brek is essential for a late stage of spermatogenesis. Further clarification of the mechanism by which Brek regulates spermatogenesis may help identify new targets for reproductive contraceptives and treatments against infertility.
引用
收藏
页码:19344 / 19349
页数:6
相关论文
empty
未找到相关数据