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通过IGF-1生成试验研究生长激素敏感性的遗传和表观遗传调控。

Genetic and Epigenetic Modulation of Growth Hormone Sensitivity Studied With the IGF-1 Generation Test.

作者信息

Ouni Meriem, Castell Anne-Laure, Linglart Agnès, Bougnères Pierre

机构信息

Institut National de la Santé et de la Recherche Médicale Unité 986 (M.O., A.-L.C., A.L., P.B.) and Department of Pediatric Endocrinology and Diabetes (A.-L.C., A.L., P.B.), Paris Sud University, Bicêtre Hospital, 94275 Le Kremlin-Bicêtre, France.

出版信息

J Clin Endocrinol Metab. 2015 Jun;100(6):E919-25. doi: 10.1210/jc.2015-1413. Epub 2015 Apr 2.

Abstract

CONTEXT

Like all hormones, GH has variable physiological effects across people. Many of these effects initiated by the binding of GH to its receptor (GHR) in target tissues are mediated by the expression of the IGF1 gene. Genetic as well as epigenetic variation is known to contribute to the individual diversity of GH-dependent phenotypes through two mechanisms. The first one is the genetic polymorphism of the GHR gene due to the common deletion of exon 3. The second, more recently reported, is the epigenetic variation in the methylation of a cluster of CGs dinucleotides located within the proximal part of the P2 promoter of the IGF-1 (IGF1) gene, notably CG-137.

OBJECTIVE

The current study evaluates the relative contribution of these two factors controlling individual GH sensitivity by measuring the response of serum IGF-1 to a GH injection (IGF-1 generation test) in a sample of 72 children with idiopathic short stature.

RESULTS

Although the d3 polymorphism of the GHR contributed 19% to the variance of the IGF-1 response, CG-137 methylation in the IGF-1 promoter contributed 30%, the combined contribution of the two factors totaling 43%.

CONCLUSION

Our observation indicates that genetic and epigenetic variation at the GHR and IGF-1 loci play a major role as independent modulators of individual GH sensitivity.

摘要

背景

与所有激素一样,生长激素(GH)在不同个体中具有不同的生理效应。生长激素与其在靶组织中的受体(GHR)结合引发的许多效应是由胰岛素样生长因子1(IGF1)基因的表达介导的。已知遗传变异以及表观遗传变异通过两种机制导致生长激素依赖性表型的个体差异。第一种是由于外显子3的常见缺失导致的GHR基因的遗传多态性。第二种,也是最近报道的,是位于IGF-1(IGF1)基因P2启动子近端的一组CG二核苷酸甲基化的表观遗传变异,特别是CG-137。

目的

本研究通过测量72名特发性身材矮小儿童样本中血清IGF-1对GH注射的反应(IGF-1生成试验),评估这两个控制个体生长激素敏感性的因素的相对贡献。

结果

虽然GHR的d3多态性对IGF-1反应的方差贡献了19%,但IGF-1启动子中的CG-137甲基化贡献了30%,这两个因素的综合贡献总计43%。

结论

我们的观察表明,GHR和IGF-1基因座的遗传和表观遗传变异作为个体生长激素敏感性的独立调节因子发挥着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3ae/4454803/3acb1377dd70/zeg9991517590001.jpg

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