University of Cambridge Metabolic Research Laboratories, Level 4, Wellcome Trust-Medical Research Council Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge CB2 0QQ, United Kingdom.
Cambridge Institute for Medical Research, University of Cambridge, Cambridge CB2 0QQ, United Kingdom.
Proc Natl Acad Sci U S A. 2017 Aug 29;114(35):9421-9426. doi: 10.1073/pnas.1707310114. Epub 2017 Aug 15.
An intergenic region of human chromosome 2 (2p25.3) harbors genetic variants which are among those most strongly and reproducibly associated with obesity. The gene closest to these variants is , although the molecular mechanisms mediating these effects remain entirely unknown. expression in the murine hypothalamic paraventricular nucleus (PVN) was altered by changes in nutritional state. Germline loss of in mice resulted in increased body weight, which was exacerbated by high fat diet and driven by increased food intake. Selective overexpression of in the PVN of wild-type mice reduced food intake and also increased energy expenditure. We provide evidence that TMEM18 has four, not three, transmembrane domains and that it physically interacts with key components of the nuclear pore complex. Our data support the hypothesis that itself, acting within the central nervous system, is a plausible mediator of the impact of adjacent genetic variation on human adiposity.
人类 2 号染色体(2p25.3)上的一个基因间区域含有遗传变异,这些变异与肥胖的相关性最强且最具可重复性。这些变异最接近的基因是 ,尽管介导这些影响的分子机制仍然完全未知。在营养状态改变时, 在鼠下丘脑室旁核(PVN)中的表达发生改变。在小鼠中, 的种系缺失导致体重增加,高脂肪饮食会加重这种情况,其驱动力是食物摄入量增加。在野生型小鼠的 PVN 中选择性过表达 会减少食物摄入,同时增加能量消耗。我们提供的证据表明,TMEM18 有四个而不是三个跨膜结构域,并且它与核孔复合物的关键组成部分发生物理相互作用。我们的数据支持这样一种假设,即 本身在中枢神经系统中起作用,是相邻遗传变异对人类肥胖影响的合理介导者。