MOLECULAR-STRUCTURE OF TCP-10 GENES FROM THE T-COMPLEX RESPONDER LOCUS

被引:13
作者
BULLARD, DC [1 ]
SCHIMENTI, JC [1 ]
机构
[1] CASE WESTERN RESERVE UNIV,DEPT GENET,CLEVELAND,OH 44106
关键词
D O I
10.1007/BF00352329
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Male transmission ratio distortion (TRD) is a property of mouse t haplotypes which requires the t complex responder locus (Tcr). Tcr has been localized to a 70-160 kb region in t haplotypes. A candidate gene for the responder, called Tcp-10b(t), has been cloned and is one member of a highly related gene family called Tcp-10 (formerly T66). Molecular evidence suggests that unique alternative splicing of the Tcp-10b(t) gene may be responsible for the mutant responder activity. Here we present the intron/exon structure of a representative Tcp-10 gene, and the characterization of alternative polyadenylation sites. The Tcp-10 genes contain 12 exons which span approximately 21 kb of DNA. At least six different polyadenylation sites are used, and none have a perfect consensus signal. This appears to be a common feature associated with testes-expressed transcripts. Since the gene we have analyzed is absent from many t haplotypes without apparent consequence, and no corresponding cDNAs have been isolated, it was speculated to be a pseudogene. However, no major sequence differences were found within the coding sequence to conclude that Tcp-10ps(t) is a pseudogene.
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页码:228 / 234
页数:7
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