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小鼠X染色体上体重基因座的定位

Mapping of body weight loci on mouse chromosome X.

作者信息

Dragani T A, Zeng Z B, Canzian F, Gariboldi M, Ghilarducci M T, Manenti G, Pierotti M A

机构信息

Division of Experimental Oncology A, Instituto Nazionale Tumori, Milan, Italy.

出版信息

Mamm Genome. 1995 Nov;6(11):778-81. doi: 10.1007/BF00539002.

Abstract

Inheritance of overweight in humans appears to be under polygenic control. Study on the mouse model may help to determine candidate regions in human genome for the search of overweight genes. Inbred mouse strains showed wide variation in body weight and can provide an experimental model for the study of inheritance of overweight. By genetic linkage analysis, we report the mapping of two loci, named Bw1 and Bw2 (body weight 1 and 2), on Chromosome (Chr) X that strongly affect adult body weight in two interspecific testcross male populations (HSB) and ASB) of mice. In addition, another locus, named Bw3, is also mapped on Chr X in ASB populations. These loci account for up to 24% of the phenotypic variation in both populations. Considering the conserved synteny between mouse and humans Chr X, these results provide candidate regions on Chr X that can be tested for linkage with overweight in humans.

摘要

人类超重的遗传似乎受多基因控制。对小鼠模型的研究可能有助于确定人类基因组中的候选区域,以寻找超重基因。近交系小鼠品系在体重上表现出广泛的差异,可为超重遗传研究提供实验模型。通过遗传连锁分析,我们报告了在小鼠的两个种间测交雄性群体(HSB和ASB)中,位于X染色体上的两个位点Bw1和Bw2(体重1和2)的定位,这两个位点对成年体重有强烈影响。此外,在ASB群体中,另一个名为Bw3的位点也定位在X染色体上。这些位点在两个群体中占表型变异的比例高达24%。考虑到小鼠和人类X染色体之间保守的同线性,这些结果提供了X染色体上的候选区域,可用于检测与人类超重的连锁关系。

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