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小鼠ob基因突变的分子定位

Molecular mapping of the mouse ob mutation.

作者信息

Friedman J M, Leibel R L, Siegel D S, Walsh J, Bahary N

机构信息

Howard Hughes Medical Institute, Rockefeller University, New York, New York 10021.

出版信息

Genomics. 1991 Dec;11(4):1054-62. doi: 10.1016/0888-7543(91)90032-a.

Abstract

The mouse ob mutation has been mapped relative to a series of RFLPs among the progeny of three separate mouse crosses: an intraspecific backcross, an intraspecific intercross, and an interspecific intercross. Genotypic assignment at the ob locus was made by making use of measurements of body mass index and the plasma concentrations of glucose and insulin. These data have suggested that the development of diabetes in these animals is a consequence of unlinked polygenes. There was also evidence that unlinked Mus spretus alleles can diminish the obesity of ob/ob mice. From these data we have mapped several markers on chromosome 6 with the following order: cen-Cola-2-Met-ob-Cpa-Tcrb. The homologs of markers that flank ob map to human chromosome 7q, suggesting that if there is a human homologue of ob, it maps to 7q31.

摘要

小鼠ob突变已相对于三个独立小鼠杂交后代中的一系列限制性片段长度多态性(RFLP)进行了定位:种内回交、种内杂交和种间杂交。通过测量体重指数以及葡萄糖和胰岛素的血浆浓度来确定ob位点的基因型。这些数据表明,这些动物患糖尿病是不连锁多基因的结果。也有证据表明,不连锁的小家鼠等位基因可以减轻ob/ob小鼠的肥胖。根据这些数据,我们在6号染色体上定位了几个标记,顺序如下:着丝粒-Cola-2-Met-ob-Cpa-Tcrb。位于ob两侧的标记的同源物定位于人类7号染色体q区,这表明如果存在ob的人类同源物,它定位于7q31。

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