4.2 Article

Metabolic impact of sex chromosomes

期刊

ADIPOCYTE
卷 2, 期 2, 页码 74-79

出版社

TAYLOR & FRANCIS INC
DOI: 10.4161/adip.23320

关键词

metabolic disease; sex differences; obesity; food intake; fatty liver; circadian rhythm

资金

  1. National Institute of Diabetes and Digestive and Kidney Diseases (National Public Health Service) [R01 DK83561]
  2. Ruth L. Kirschstein National Research Service Award [GM007185]
  3. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK083561] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Obesity and associated metabolic diseases are sexually dimorphic. To provide better diagnosis and treatment for both sexes, it is of interest to identify the factors that underlie male/female differences in obesity. Traditionally, sexual dimorphism has been attributed to effects of gonadal hormones, which influence numerous metabolic processes. However, the XX/XY sex chromosome complement is an additional factor that may play a role. Recent data using the four core genotypes mouse model have revealed that sex chromosome complement-independently from gonadal sex-plays a role in adiposity, feeding behavior, fatty liver and glucose homeostasis. Potential mechanisms for the effects of sex chromosome complement include differential gene dosage from X chromosome genes that escape inactivation, and distinct genomic imprints on X chromosomes inherited from maternal or paternal parents. Here we review recent data in mice and humans concerning the potential impact of sex chromosome complement on obesity and metabolic disease.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据