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肥胖症12个候选基因的微卫星标记内容图谱:用于自动基因分型的七个肥胖症筛查面板的组装

Microsatellite marker content mapping of 12 candidate genes for obesity: assembly of seven obesity screening panels for automated genotyping.

作者信息

Winick J D, Friedman J M

机构信息

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

出版信息

Genome Res. 1998 Sep;8(9):985-94. doi: 10.1101/gr.8.9.985.

Abstract

Twin studies, adoption studies, and studies of familial aggregation indicate that obesity has a genetic component. Whereas, the genetic factors predisposing to obesity have been elucidated for several rare syndromes, the factors responsible for obesity in the general population have remained elusive. Genetic studies of complex traits are often accelerated by the use of candidate genes. To facilitate genetic studies of human obesity, seven multiplex panels of candidate genes for obesity that are suitable for fluorescent genotyping have been assembled. The multiplex panels are composed of 66 microsatellite markers linked tightly to 16 human gene products that are of potential importance in the control of body weight or linked to syndromic forms of obesity. As part of these efforts 12 previously cloned genes have been placed on the human physical map. In addition the chromosomal location of three of these genes, ART, NYP Y6R, and PPARgamma, are reported for the first time. These resources will be of use in studies to identify the genetic factors responsible for human obesity. [Figures are available at http://www.genome.org]

摘要

双胞胎研究、收养研究以及家族聚集性研究表明,肥胖具有遗传因素。虽然导致几种罕见综合征的肥胖遗传因素已得到阐明,但导致普通人群肥胖的因素仍然难以捉摸。复杂性状的遗传研究通常通过使用候选基因来加速。为促进人类肥胖的遗传研究,已组装了七个适合荧光基因分型的肥胖候选基因多重面板。这些多重面板由66个微卫星标记组成,这些标记与16种人类基因产物紧密相连,这些基因产物在体重控制中具有潜在重要性或与肥胖综合征形式相关。作为这些工作的一部分,12个先前克隆的基因已被定位到人类物理图谱上。此外,首次报道了其中三个基因ART、NYP Y6R和PPARγ的染色体定位。这些资源将用于识别导致人类肥胖的遗传因素的研究。[图表可在http://www.genome.org获取]

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