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犹他州系谱中体重指数与20号染色体的连锁关系。

Linkage of body mass index to chromosome 20 in Utah pedigrees.

作者信息

Hunt S C, Abkevich V, Hensel C H, Gutin A, Neff C D, Russell D L, Tran T, Hong X, Jammulapati S, Riley R, Weaver-Feldhaus J, Macalma T, Richards M M, Gress R, Francis M, Thomas A, Frech G C, Adams T D, Shattuck D, Stone S

机构信息

Cardiovascular Genetics, University of Utah, 410 Chipeta Way RM 167, Salt Lake City, UT 84108, USA.

出版信息

Hum Genet. 2001 Sep;109(3):279-85. doi: 10.1007/s004390100581.

Abstract

Several linkage studies have hinted at the existence of an obesity predisposition locus on chromosome 20, but none of these studies has produced conclusive results. Therefore, we analyzed 48 genetic markers on chromosome 20 for linkage to severe obesity (BMI> or =35) in 103 extended Utah pedigrees (1,711 individuals), all of which had strong aggregation of severe obesity. A simple dominant model produced a maximum multipoint heterogeneity LOD score of 3.5 at D20S438 (55.1 cM). Two additional analyses were performed. First, a one-gene, two-mutation model (with one dominant mutation and one recessive mutation) increased the LOD score to 4.2. Second, a two-locus model (with one locus dominant and one recessive) generated a multipoint LOD score of 4.9. We conclude that one or more severe obesity predisposing genes lie within an interval of approx. 10 cM on chromosome 20. This study generated significant LOD scores which confirm suggestive linkage reports from previous studies. In addition, our analyses suggest that the predisposing gene(s) is localized very near the chromosome 20 centromere.

摘要

多项连锁研究已暗示20号染色体上存在肥胖易感基因座,但这些研究均未得出确凿结果。因此,我们在103个犹他州扩展家系(1711人)中分析了20号染色体上的48个遗传标记与重度肥胖(BMI≥35)的连锁关系,所有家系中重度肥胖都有很强的聚集性。一个简单的显性模型在D20S438(55.1 cM)处产生了最大多点异质性LOD分数为3.5。进行了另外两项分析。首先,一个单基因、双突变模型(一个显性突变和一个隐性突变)将LOD分数提高到4.2。其次,一个双基因座模型(一个基因座显性和一个隐性)产生了多点LOD分数为4.9。我们得出结论,一个或多个重度肥胖易感基因位于20号染色体上约10 cM的区间内。这项研究产生了显著的LOD分数,证实了先前研究中提示的连锁报道。此外,我们的分析表明,易感基因定位在非常靠近20号染色体着丝粒的位置。

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