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Microsatellite Marker Content Mapping of 12 Candidate Genes for Obesity: Assembly of Seven Obesity Screening Panels for Automated Genotyping

机译:肥胖的12个候选基因的微卫星标记内容定位:自动基因分型的七个肥胖筛查面板的组装

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摘要

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 PPARγ, 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.]
机译:孪生研究,收养研究和家族聚集研究表明,肥胖具有遗传成分。尽管已经阐明了导致肥胖的遗传因素是几种罕见的综合征,但在一般人群中导致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。为了促进对人类肥胖症的遗传研究,已经组装了七个适合荧光基因分型的肥胖症候选基因的多重面板。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,而16种人类基因产物在控制体重方面可能具有重要意义,或者与肥胖症的症状有关。作为这些工作的一部分,已将12个先前克隆的基因放置在人体图谱上。另外,首次报道了这三个基因ART,NYP Y6R和PPARγ的染色体位置。这些资源将在研究中用于识别导致人类肥胖的遗传因素。 [有关数字,请访问http://www.genome.org。]

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