COMPARATIVE MAPPING ON THE MOUSE AND HUMAN X-CHROMOSOMES OF A HUMAN CDNA CLONE ENCODING THE VASOPRESSIN RENAL-TYPE RECEPTOR (AVP2R)

被引:6
作者
FAUST, CJ
GONZALES, JC
SEIBOLD, A
BIRNBAUMER, M
HERMAN, GE
机构
[1] BAYLOR COLL MED,INST MOLEC GENET,1 BAYLOR PLAZA,S911,HOUSTON,TX 77030
[2] BAYLOR COLL MED,DEPT CELL BIOL,HOUSTON,TX 77030
[3] BAYLOR COLL MED,DEPT PEDIAT,HOUSTON,TX 77030
关键词
D O I
10.1006/geno.1993.1085
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
Mutations in the gene for the human renal-type vasopressin receptor (V2R) have recently been identified in patients with nephrogenic diabetes insipidus (NDI). Both V2R and NDI have been independently mapped to Xq28. Using a combination of genetic and physical mapping, we have localized the murine V2r locus to within 100 kb of L1Cam on the mouse X chromosome in a region syntenic with human Xq28. Based on conserved gene order of mouse and human loci in this region, physical mapping using DNA derived from human lymphoblasts has established that the corresponding human loci V2R and L1CAM are linked within 210 kb. The efficiency and precision of genetic mapping of V2r and other loci in the mouse suggest that it might be easier to map additional human genes in the mouse first and infer the corresponding human location. More precise physical mapping in man could then be performed using pulsed-field gel electrophoresis and/or yeast artificial chromosomes. © 1993 Academic Press. All rights reserved.
引用
收藏
页码:439 / 441
页数:3
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