MOLECULAR-CLONING OF THE T-COMPLEX RESPONDER GENETIC-LOCUS

被引:23
作者
ROSEN, LL
BULLARD, DC
SILVER, LM
SCHIMENTI, JC
机构
[1] CASE WESTERN RESERVE UNIV,DEPT GENET,2119 ABINGTON RD,CLEVELAND,OH 44106
[2] PRINCETON UNIV,DEPT BIOL SCI,PRINCETON,NJ 08544
关键词
D O I
10.1016/0888-7543(90)90235-M
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Although mouse t haplotypes carry recessive mutations causing male sterility and embryonic lethality, they persist in wild mouse populations via male transmission ratio distortion (TRD). Genetic evidence suggests that at least five t-haplotype-encoded loci combine to cause TRD. One of these loci, called the t complex responder (Tcr), is absolutely required for any deviation from Mendelian segregation to occur. A candidate for the Tcr gene has previously been identified. Evidence that this gene represents Tcr is its localization to the appropriate genomic subregion and testis-specific expression pattern. Here, we report the molecular cloning of the region between recombinant chromosome breakpoints defining the Tcr locus. These results circumacribe Tcr to a 150- to 220-kb region of DNA, including the 22-kb candidate responder gene. This gene and two other homologs were created by large genomic duplications, each involving segments of DNA 10-fold larger than the individual genes. © 1990.
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页码:134 / 140
页数:7
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