DETERMINATION OF A MOLECULAR MAP POSITION FOR HYP USING A NEW INTERSPECIFIC BACKCROSS PRODUCED BY INVITRO FERTILIZATION

被引:16
作者
KAY, G
THAKKER, RV
RASTAN, S
机构
[1] MRC,CLIN RES CTR,COMPARAT BIOL SECT,WATFORD RD,HARROW HA1 3UJ,MIDDX,ENGLAND
[2] MRC,CLIN RES CTR,DIV MOLEC MED,HARROW HA1 3UJ,MIDDX,ENGLAND
关键词
D O I
10.1016/0888-7543(91)90072-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
We have established a Mus spretus/Mus musculus domesticus interspecific backcross segregating for two X-linked mutant genes, Ta and Hyp, using in vitro fertilization. The haplotype of the recombinant X chromosome of each of 241 backcross progeny has been established using the X-linked anchor loci Otc, Hprt, Dmd, Pgk-1, and Amg and the additional probes DXSmh43 and Cbx-rs1. The Hyp locus (putative homologue of the human disease gene hypophosphatemic rickets, HYP) has been incorporated into the molecular genetic map of the X chromosome. We show that the most likely gene order in the distal portion of the mouse X chromosome is Pgk-1-DXSmh43-Hyp-Cbx-rs1-Amg, from proximal to distal. The distance in centimorgans (mean ± SE) between DXSmh43 and Hyp was 2.52 ± 1.4 and that between Hyp and Cbx-rs1 was 1.98 ± 1.39. Thus closely linked flanking markers for the Hyp locus that will facilitate the molecular characterization of the gene itself have been defined. © 1991.
引用
收藏
页码:651 / 657
页数:7
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