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Ia型假性甲状旁腺功能减退症:Gsα基因第5和10外显子中的两个新的杂合移码突变。

Pseudohypoparathyroidism type Ia: two new heterozygous frameshift mutations in exons 5 and 10 of the Gs alpha gene.

作者信息

Shapira H, Mouallem M, Shapiro M S, Weisman Y, Farfel Z

机构信息

Biochemical Pharmacology Laboratory, Sheba Medical Center, Tel Hashome, Israel.

出版信息

Hum Genet. 1996 Jan;97(1):73-5. doi: 10.1007/BF00218836.

Abstract

Pseudohypoparathyroidism type Ia (PHP-Ia) is a hereditary disease characterized by resistance to PTH and other hormones that act via cAMP. Patients have deficient activity of Gs alpha, the alpha subunit of the G protein, which couples hormone receptors to stimulation of adenylate cyclase. We describe two new mutations discovered in two sporadic patients with PHP-Ia. Using genomic DNA, we have amplified exons 2-13 of the Gs alpha gene (GNAS1) by PCR, and sequenced the resulting products. Both patients had Albright's hereditary osteodystrophy, resistance to multiple hormones, and deficient Gs alpha activity. In the first patient, a deletion of a C in exon 5 at codon 115 was found. In the second patient, an insertion of a C in exon 10 at codon 267 was detected. Both these heterozygous mutations cause frameshift, and predict decreased production of Gs alpha. This report adds two new Gs alpha mutations to the known ten mutations recently described.

摘要

I型假性甲状旁腺功能减退症(PHP-Ia)是一种遗传性疾病,其特征是对甲状旁腺激素(PTH)和其他通过环磷酸腺苷(cAMP)起作用的激素产生抵抗。患者的G蛋白α亚基Gsα活性不足,该亚基将激素受体与腺苷酸环化酶的刺激偶联起来。我们描述了在两名散发性PHP-Ia患者中发现的两个新突变。我们使用基因组DNA,通过聚合酶链反应(PCR)扩增了Gsα基因(GNAS1)的第2至13外显子,并对所得产物进行了测序。两名患者均患有奥尔布赖特遗传性骨营养不良症,对多种激素产生抵抗,且Gsα活性不足。在第一名患者中,发现第5外显子第115密码子处的一个C缺失。在第二名患者中,检测到第10外显子第267密码子处插入了一个C。这两个杂合突变均导致移码,并预测Gsα的产生会减少。本报告在最近描述的已知10种突变的基础上又增加了两种新的Gsα突变。

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