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罕见拷贝数和序列变异揭示的与严重早发性肥胖相关的新基因。

Novel genes involved in severe early-onset obesity revealed by rare copy number and sequence variants.

作者信息

Serra-Juhé Clara, Martos-Moreno Gabriel Á, Bou de Pieri Francesc, Flores Raquel, González Juan R, Rodríguez-Santiago Benjamín, Argente Jesús, Pérez-Jurado Luis A

机构信息

Genetics Unit, Universitat Pompeu Fabra, Barcelona, Spain.

Hospital del Mar Research Institute (IMIM), Barcelona, Spain.

出版信息

PLoS Genet. 2017 May 10;13(5):e1006657. doi: 10.1371/journal.pgen.1006657. eCollection 2017 May.

Abstract

Obesity is a multifactorial disorder with high heritability (50-75%), which is probably higher in early-onset and severe cases. Although rare monogenic forms and several genes and regions of susceptibility, including copy number variants (CNVs), have been described, the genetic causes underlying the disease still remain largely unknown. We searched for rare CNVs (>100kb in size, altering genes and present in <1/2000 population controls) in 157 Spanish children with non-syndromic early-onset obesity (EOO: body mass index >3 standard deviations above the mean at <3 years of age) using SNP array molecular karyotypes. We then performed case control studies (480 EOO cases/480 non-obese controls) with the validated CNVs and rare sequence variants (RSVs) detected by targeted resequencing of selected CNV genes (n = 14), and also studied the inheritance patterns in available first-degree relatives. A higher burden of gain-type CNVs was detected in EOO cases versus controls (OR = 1.71, p-value = 0.0358). In addition to a gain of the NPY gene in a familial case with EOO and attention deficit hyperactivity disorder, likely pathogenic CNVs included gains of glutamate receptors (GRIK1, GRM7) and the X-linked gastrin-peptide receptor (GRPR), all inherited from obese parents. Putatively functional RSVs absent in controls were also identified in EOO cases at NPY, GRIK1 and GRPR. A patient with a heterozygous deletion disrupting two contiguous and related genes, SLCO4C1 and SLCO6A1, also had a missense RSV at SLCO4C1 on the other allele, suggestive of a recessive model. The genes identified showed a clear enrichment of shared co-expression partners with known genes strongly related to obesity, reinforcing their role in the pathophysiology of the disease. Our data reveal a higher burden of rare CNVs and RSVs in several related genes in patients with EOO compared to controls, and implicate NPY, GRPR, two glutamate receptors and SLCO4C1 in highly penetrant forms of familial obesity.

摘要

肥胖是一种具有高遗传度(50 - 75%)的多因素疾病,在早发性和严重病例中可能更高。尽管已经描述了罕见的单基因形式以及几个易感基因和区域,包括拷贝数变异(CNV),但该疾病的遗传原因在很大程度上仍然未知。我们使用单核苷酸多态性(SNP)阵列分子核型分析,在157名患有非综合征性早发性肥胖(EOO:3岁前体重指数高于均值3个标准差以上)的西班牙儿童中搜索罕见的CNV(大小>100kb,改变基因且在<1/2000的人群对照中出现)。然后,我们对通过对选定的CNV基因(n = 14)进行靶向重测序检测到的经过验证的CNV和罕见序列变异(RSV)进行病例对照研究(480例EOO病例/480名非肥胖对照),并研究了可用的一级亲属中的遗传模式。与对照相比,在EOO病例中检测到更高的获得型CNV负担(比值比 = 1.71,p值 = 0.0358)。除了在一名患有EOO和注意力缺陷多动障碍的家族病例中NPY基因的获得外,可能致病的CNV还包括谷氨酸受体(GRIK1、GRM7)和X连锁胃泌素肽受体(GRPR)的获得,所有这些都是从肥胖父母遗传而来。在EOO病例的NPY、GRIK1和GRPR中也鉴定出对照中不存在的假定功能性RSV。一名杂合缺失破坏了两个相邻且相关基因SLCO4C1和SLCO6A1的患者,在另一个等位基因的SLCO4C1上也有一个错义RSV,提示隐性模式。所鉴定的基因显示与已知与肥胖密切相关的基因共享共表达伙伴明显富集,强化了它们在疾病病理生理学中的作用。我们的数据显示,与对照相比,EOO患者中几个相关基因的罕见CNV和RSV负担更高,并表明NPY、GRPR、两种谷氨酸受体和SLCO4C1在家族性肥胖的高外显形式中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e47d/5443539/490f1fada9f5/pgen.1006657.g001.jpg

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