Mouse platelet-derived growth factor receptor alpha gene is deleted in W19H and patch mutations on chromosome 5.
Mouse platelet-derived growth factor receptor alpha gene is deleted in W19H and patch mutations on chromosome 5.
复制标题
小鼠血小板源性生长因子受体 α 基因在 W19H 中被删除,并在 5 号染色体上发生补丁突变。
DOI:
10.1073/pnas.88.11.4811
复制
发表时间:
1991
影响因子:
11.1
通讯作者:
Naylor,SL
中科院分区:
文献类型:
--
作者:
Smith,EA;Seldin,MF;Martinez,L;Watson,ML;Choudhury,GG;Lalley,PA;Pierce,J;Aaronson,S;Barker,J;Naylor,SL
The mouse W19H mutation is an x-ray-induced deletion of more than 2 centimorgans on chromosome 5 encompassing the white spotting mutation W (encoded by the Kit protooncogene), patch (Ph), and recessive lethal (l) loci. The platelet-derived growth factor receptor alpha gene (PDGFRA) like Kit encodes a transmembrane receptor tyrosine kinase. By using mouse-Chinese hamster somatic cell hybrids and haplotype analysis in interspecific backcross mice, mouse Pdgfra was mapped to chromosome 5 in tight linkage with Kit. Hybridization of a PDGFRA probe to DNAs from W19H/ + heterozygous mice and patch heterozygous mice, and their wild-type littermates, demonstrated deletion of Pdgfra. Pulsed-field gel electrophoresis indicated that Kit and Pdgfra are linked on a 630-kilobase Mlu I DNA fragment. Thus the W19H deletion removes at least two receptor tyrosine kinases and the results suggest Pdgfra as a candidate for the Ph locus.