Levine M A, Ahn T G, Klupt S F, Kaufman K D, Smallwood P M, Bourne H R, Sullivan K A, Van Dop C
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Proc Natl Acad Sci U S A. 1988 Jan;85(2):617-21. doi: 10.1073/pnas.85.2.617.
Patients who have pseudohypoparathyroidism type I associated with Albright hereditary osteodystrophy commonly have a genetic deficiency of the alpha subunit of the G protein that stimulates adenylyl cyclase (alpha Gs) (ATP pyrophosphate-lyase, EC 4.6.1.1). To discover the molecular mechanism that causes alpha Gs deficiency in these patients, we examined eight kindreds with one or more members affected with Albright hereditary osteodystrophy or pseudohypoparathyroidism and alpha Gs deficiency. In these families, alpha Gs deficiency and the Albright hereditary osteodystrophy phenotype were transmitted together in a dominant inheritance pattern. Using a cDNA hybridization probe for alpha Gs, restriction analysis with several endonucleases showed no abnormalities of restriction fragments or gene dosage. RNA blot and dot blot analysis of total RNA from cultured fibroblasts obtained from the patients revealed approximately equal to 50% reduced mRNA levels for alpha Gs in affected members of six of the pedigrees but normal levels in affected members of the two other pedigrees, compared to mRNA levels in fibroblasts from unaffected individuals. By contrast, mRNA levels encoding the alpha subunit of the G protein that inhibits adenylyl cyclase were not altered. Our findings suggest that several molecular mechanisms produce alpha Gs deficiency in patients with pseudohypoparathyroidism type Ia and that major gene rearrangements or deletions are not a common cause for alpha Gs deficiency in pseudohypoparathyroidism type I.
患有与奥尔布赖特遗传性骨营养不良相关的I型假性甲状旁腺功能减退症的患者,通常存在刺激腺苷酸环化酶的G蛋白α亚基(αGs)(ATP焦磷酸裂解酶,EC 4.6.1.1)的基因缺陷。为了发现导致这些患者αGs缺陷的分子机制,我们研究了8个家系,这些家系中有一个或多个成员患有奥尔布赖特遗传性骨营养不良或假性甲状旁腺功能减退症以及αGs缺陷。在这些家族中,αGs缺陷和奥尔布赖特遗传性骨营养不良表型以显性遗传模式共同传递。使用针对αGs的cDNA杂交探针,用几种核酸内切酶进行的限制性分析未显示限制性片段或基因剂量有异常。对从患者获得的培养成纤维细胞的总RNA进行RNA印迹和斑点印迹分析显示,与未受影响个体的成纤维细胞中的mRNA水平相比,六个家系中受影响成员的αGs mRNA水平降低了约50%,但另外两个家系中受影响成员的mRNA水平正常。相比之下,编码抑制腺苷酸环化酶的G蛋白α亚基的mRNA水平没有改变。我们的研究结果表明,几种分子机制导致Ia型假性甲状旁腺功能减退症患者出现αGs缺陷,并且主要的基因重排或缺失不是I型假性甲状旁腺功能减退症中αGs缺陷的常见原因。