Truett G E, Bahary N, Friedman J M, Leibel R L
Laboratory of Human Behavior and Metabolism, Rockefeller University, New York, NY 10021.
Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7806-9. doi: 10.1073/pnas.88.17.7806.
The autosomal recessive mutations fa (rat) and db (mouse) cause obesity syndromes that develop early and ultimately become severe. Although both fa/fa rats and db/db mice have been studied extensively as models of human obesity and diabetes, the molecular bases of these phenotypes remain unknown. We have mapped fa in 50 fa/fa (obese) offspring of a (13M x Brown Norway) F1 fa/+ intercross relative to two molecular markers, Ifa and Glut-1, which flank db on mouse chromosome 4 and which are located on rat chromosome 5. Ifa and Glut-1 are linked to fa, with a gene order, Ifa-fa-Glut-1, that is identical to that for the region around db in the mouse genome. These results place fa on rat chromosome 5 and suggest that db and fa are mutations in homologous genes.
常染色体隐性突变fa(大鼠)和db(小鼠)会引发早期出现且最终会变得严重的肥胖综合征。尽管fa/fa大鼠和db/db小鼠作为人类肥胖和糖尿病的模型已被广泛研究,但这些表型的分子基础仍不清楚。我们在(13M×棕色挪威大鼠)F1 fa/+杂交的50只fa/fa(肥胖)后代中,相对于两个分子标记Ifa和Glut-1对fa进行了定位,这两个标记位于小鼠4号染色体上db的两侧,且位于大鼠5号染色体上。Ifa和Glut-1与fa连锁,基因顺序为Ifa-fa-Glut-1,这与小鼠基因组中db周围区域的基因顺序相同。这些结果将fa定位在大鼠5号染色体上,并表明db和fa是同源基因中的突变。