A HIGH-RESOLUTION MAP OF THE CHROMOSOMAL REGION SURROUNDING THE NUDE GENE
Details
Publication Year 1995-03-20,Volume 26,Issue #2,Page 308-317
Journal Title
GENOMICS
Publication Type
Journal Article
Abstract
The nude mutation produces the apparently disparate phenotypes of hairlessness and congenital thymic aplasia. These pleiotropic defects are the result of a single, autosomal recessive mutation that was previously mapped to a 9-cM region of murine chromosome 11 bounded by loci encoding the acetylcholine receptor beta subunit and myeloperoxidase. In this study, exclusion mapping of a panel of congenic nude strains was used to place the nude locus between the microsatellite loci D11Nds1 and D11Mit8. The relative distance from nude to each of these loci was determined by analyzing a large segregating cross. Thus, nude lies 1.4 cM distal to D11Nds1 and is 0.5 cM proximal to D11Mit8. Mice that carried recombinational breakpoints between D11Nds1 and D11Mit8 were further analyzed at the loci Evi-2 and D11Mit34, which placed nu 0.2 cM proximal to these markers. D11Nds1 and Evi-2/D11Mit34 thus define the new proximal and distal boundaries, respectively, for the nu interval. We also report the typing of the above microsatellite markers in the AKXD, AKXL, BXD, CXB, and BXH recombinant inbred strains, which confirmed the relative order and separation of loci in this region. (C) 1995 Academic Press, Inc.
Publisher
ACADEMIC PRESS INC JNL-COMP SUBSCRIPTIONS
Keywords
RECOMBINANT INBRED STRAINS; TYPE-1 NEUROFIBROMATOSIS GENE; MOUSE CHROMOSOME-11; LOCALIZATION; LINKAGE; MICE; PROVIRUSES; ASSIGNMENT; PROTEIN; IDENTIFICATION
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 1995-03-20 12:00:00
An error has occurred. This application may no longer respond until reloaded. Reload 🗙