High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and waltzer (Cdh23v)

被引:29
作者
Bryda, EC
Kim, HJ
Legare, ME
Frankel, WN
Noben-Trauth, K
机构
[1] Natl Inst Deafness & Other Commun Disorders, Unit Neurogenet, NIH, Rockville, MD 20850 USA
[2] Marshall Univ, Sch Med, Dept Microbiol Mol Genet & Immunol, Huntington, WV 25704 USA
[3] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
D O I
10.1006/geno.2001.6538
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
Modifier-of-deafwaddler (mdfw) and waltzer (Cdh23(v)) are loci on mouse chromosome 10 encoding factors that are essential for the function of auditory hair cells. The BALB/cByJ-specific mdfw allele encodes a necessary and sufficient modifier that induces progressive early onset hearing loss in CBy-dfw(2J) heterozygotes. Recessive mutations in the waltzer locus result in:circling behavior and congenital deafness. In this report we present a high-resolution integrated genetic and physical map of mdfw and Cdh23(v). Our genetic analyses localize mdfw, between markers D10Mit60 and 148M13T7 within a 1.01-cM region. The Cdh23(v) critical interval is fully contained within the mdfw, region and localizes between markers 146O23T7 and 148M13T7 within a 0.35-cM interval that is represented in an approximate to 500-kb BAC contig, Our data suggest that mdfw and Cdh23(v) are allelic, (C) 2001 Academic Press.
引用
收藏
页码:338 / 342
页数:5
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