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利用对gld自身免疫突变进行分离的种间杂交构建的小鼠1号染色体连锁图谱。

A linkage map of mouse chromosome 1 using an interspecific cross segregating for the gld autoimmunity mutation.

作者信息

Watson M L, D'Eustachio P, Mock B A, Steinberg A D, Morse H C, Oakey R J, Howard T A, Rochelle J M, Seldin M F

机构信息

Department of Medicine, Duke University, Durham, North Carolina 27710.

出版信息

Mamm Genome. 1992;2(3):158-71. doi: 10.1007/BF00302874.

Abstract

An interspecific backcross was used to define a high resolution linkage map of mouse Chromosome (Chr) 1 and to analyze the segregation of the generalized lymphoproliferative disease (gld) mutation. Mice homozygous for gld have multiple features of autoimmune disease. Analysis of up to 428 progeny from the backcross [(C3H/HeJ-gld x Mus spretus)F1 x C3H/HeJ-gld] established a map that spans 77.6 cM and includes 56 markers distributed over 34 ordered genetic loci. The gld mutation was mapped to a less than 1 cM segment on distal mouse Chr 1 using 357 gld phenotype-positive backcross mice. A second backcross, between the laboratory strains C57BL/6J and SWR/J, was examined to compare recombination frequency between selected markers on mouse Chr 1. Significant differences in crossover frequency were demonstrated between the interspecific backcross and the inbred laboratory cross for the entire interval studied. Sex difference in meiotic crossover frequency was also significant in the laboratory mouse cross. Two linkage groups known to be conserved between segments of mouse Chr 1 and the long arm of human Chrs 1 and 2 where further defined and a new conserved linkage group was identified that includes markers of distal mouse Chr 1 and human Chr 1, bands q32 to q42.

摘要

通过种间回交来构建小鼠1号染色体(Chr)的高分辨率连锁图谱,并分析全身性淋巴细胞增生性疾病(gld)突变的分离情况。gld纯合子小鼠具有自身免疫性疾病的多种特征。对回交后代[(C3H/HeJ-gld×小家鼠)F1×C3H/HeJ-gld]中多达428个后代进行分析,构建了一个跨度为77.6厘摩(cM)的图谱,其中包括分布在34个有序遗传位点上的56个标记。利用357只gld表型阳性的回交小鼠,将gld突变定位到小鼠1号染色体远端小于1厘摩的区段。对实验室品系C57BL/6J和SWR/J之间的第二次回交进行了检测,以比较小鼠1号染色体上选定标记之间的重组频率。在所研究的整个区间内,种间回交和近交实验室杂交之间的交叉频率存在显著差异。在实验室小鼠杂交中,减数分裂交叉频率的性别差异也很显著。进一步明确了已知在小鼠1号染色体区段与人类1号和2号染色体长臂之间保守的两个连锁群,并鉴定出一个新的保守连锁群,其中包括小鼠1号染色体远端和人类1号染色体q32至q42带的标记。

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