A protein kinase encoded by the t complex responder gene causes non-mendelian inheritance

被引:138
作者
Herrmann, BG [1 ]
Koschorz, B [1 ]
Wertz, K [1 ]
McLaughlin, KJ [1 ]
Kispert, A [1 ]
机构
[1] Max Planck Inst Immunbiol, D-79108 Freiburg, Germany
关键词
D O I
10.1038/45970
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
Males heterozygous for the t-haplotype form of mouse chromosome 17 preferentially transmit the t-chromosome to their progeny. Several distorter/sterility loci carried on the t-haplotype together impair flagellar function in all spermatozoa whereas the responder, Tcr, rescues t-sperm but not wild-type sperm. Thus, t-sperm have an advantage over wild-type sperm in fertilizing egg cells. We have isolated Tcr by positional cloning and show that it is a member of a novel protein kinase gene family, designated Smok, which is expressed late during spermiogenesis, Smok kinases are components of a signal cascade which may control sperm motility, Tcr has a reduced kinase activity, which may allow it to counterbalance a signalling impairment caused by the distorter/sterility loci, Tcr transgene constructs cause non-mendelian transmission of chromosomes on which they are carried, which leads to sex-ratio distortion when Tcr cosegregates with the Y chromosome.
引用
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页码:141 / 146
页数:6
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