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人类GNAS1基因是印记基因,编码不同的父源表达和双等位基因表达的G蛋白。

The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins.

作者信息

Hayward B E, Kamiya M, Strain L, Moran V, Campbell R, Hayashizaki Y, Bonthron D T

机构信息

Human Genetics Unit, University of Edinburgh, Western General Hospital, Edinburgh EH4 2XU, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):10038-43. doi: 10.1073/pnas.95.17.10038.

Abstract

The GNAS1 gene encodes the alpha subunit of the G protein Gs, which couples receptor binding by several hormones to activation of adenylate cyclase. Null mutations of GNAS1 cause pseudohypoparathyroidism (PHP) type Ia, in which hormone resistance occurs in association with a characteristic osteodystrophy. The observation that PHP Ia almost always is inherited maternally has led to the suggestion that GNAS1 may be an imprinted gene. Here, we show that, although Gsalpha expression (directed by the promoter upstream of exon 1) is biallelic, GNAS1 is indeed imprinted in a promoter-specific fashion. We used parthenogenetic lymphocyte DNA to screen by restriction landmark genomic scanning for loci showing differential methylation between paternal and maternal alleles. This screen identified a region that was found to be methylated exclusively on a maternal allele and was located approximately 35 kb upstream of GNAS1 exon 1. This region contains three novel exons that are spliced into alternative GNAS1 mRNA species, including one exon that encodes the human homologue of the large G protein XLalphas. Transcription of these novel mRNAs is exclusively from the paternal allele in all tissues examined. The differential imprinting of separate protein products of GNAS1 therefore may contribute to the anomalous inheritance of PHP Ia.

摘要

GNAS1基因编码G蛋白Gs的α亚基,该亚基可将几种激素的受体结合与腺苷酸环化酶的激活偶联起来。GNAS1的无效突变会导致Ia型假性甲状旁腺功能减退症(PHP),其中激素抵抗与特征性骨营养不良相关。PHP Ia几乎总是母系遗传这一观察结果提示GNAS1可能是一个印记基因。在此,我们表明,虽然Gsα的表达(由外显子1上游的启动子指导)是双等位基因的,但GNAS1确实以启动子特异性方式被印记。我们使用孤雌生殖淋巴细胞DNA,通过限制性内切酶标记基因组扫描筛选父本和母本等位基因之间显示出差异甲基化的位点。该筛选鉴定出一个区域,该区域被发现仅在母本等位基因上甲基化,并且位于GNAS1外显子1上游约35 kb处。该区域包含三个新的外显子,它们被剪接到不同的GNAS1 mRNA种类中,包括一个编码大G蛋白XLαs的人类同源物的外显子。在所有检测的组织中,这些新mRNA的转录仅来自父本等位基因。因此,GNAS1不同蛋白质产物的差异印记可能导致PHP Ia的异常遗传。

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