MOLECULAR MAPPING OF SSRS FOR PGM1 AND C8B IN THE VICINITY OF THE RAT FATTY LOCUS

被引:17
作者
KERSHAW, EE
CHUA, SC
WILLIAMS, JA
MURPHY, EM
LEIBEL, RL
机构
[1] ROCKEFELLER UNIV,HUMAN BEHAV & METAB LAB,NEW YORK,NY 10021
[2] HOWARD HUGHES MED INST,CHEVY CHASE,MD 20815
[3] VASSAR COLL,NATL INST HLTH,ANIM MODE CORE LAB,DEPT BIOL,POUGHKEEPSIE,NY 12601
关键词
D O I
10.1006/geno.1995.1017
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
Recessive mutations at the rat fatty locus (fa, fa(cp)), which produce obesity, insulin resistance, and diabetes, provide useful experimental models for similar phenotypes in humans, The molecular pathogenesis of the metabolic phenotype in animals segregating for fa is unknown and difficult to study once the confounding metabolic effects of obesity are present. Although various experimental methods distinguish preobese from lean rats (phenotypic markers and molecular markers genetically linked 60 fatty), technical difficulties limit their utility, We report the identification of two (GT)(n) simple sequence repeats (SSRs) near the rat phosphoglucomutase gene (Pgm1) gene and two SSRs, (GA)(n) and (GT)(n), near the rat complement component 8 beta gene (C8b). These SSRs map to an similar to 4-cM interval flanking the fatty locus on rat chromosome 5, Use of these molecular markers in combination offers an improved method for early assessment of gene dosage for fa and hence for studying the fundamental molecular physiology underlying the derangements of metabolism and behavior resulting from mutations in this gene. (C) 1995 Academic Press, Inc.
引用
收藏
页码:149 / 154
页数:6
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