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[激素抵抗的基因分析]

[Genetic analysis of hormone resistance].

作者信息

Sakurai A

机构信息

Department of Geriatrics, Endocrinology, and Metabolism, Shinshu University School of Medicine, Matsumoto.

出版信息

Rinsho Byori. 1993 May;41(5):527-32.

PMID:8350516
Abstract

Thyroid hormone resistance is a syndrome defined as impaired tissue response to thyroid hormone which would be excessive under normal circumstances. Although it has long been speculated that this defect was caused by an abnormality at the site of the nuclear receptor for thyroid hormone, isolation of complementary DNA encoding thyroid hormone receptors has only recently enabled us to directly examine this hypothesis. Thyroid hormone receptors are coded on two separate genes, THRA and THRB. Both genes give rise to multiple receptor subtypes through alternative splicing or different usage of promoters. Tight linkage between THRB locus and resistant phenotype was demonstrated in one affected family, and subsequently, more than 30 genetic abnormalities of the THRB gene were isolated. No abnormalities have been demonstrated on the THRA gene. Denaturing gradient gel electrophoresis was used to screen abnormalities on the THRB gene of affected families, and the results also strongly supported the hypothesis that thyroid hormone resistance is caused by an abnormal THRB gene. Molecular analysis of thyroid hormone resistance will facilitate understanding of the pathophysiology of this syndrome and the molecular mechanism of thyroid hormone action.

摘要

甲状腺激素抵抗是一种综合征,其定义为组织对甲状腺激素的反应受损,而在正常情况下甲状腺激素反应会过度。尽管长期以来一直推测这种缺陷是由甲状腺激素核受体位点的异常引起的,但直到最近,编码甲状腺激素受体的互补DNA的分离才使我们能够直接检验这一假设。甲状腺激素受体由两个独立的基因THRA和THRB编码。这两个基因通过可变剪接或启动子的不同使用产生多种受体亚型。在一个患病家族中证实了THRB基因座与抵抗表型之间的紧密连锁,随后,分离出了30多种THRB基因的遗传异常。未在THRA基因上发现异常。使用变性梯度凝胶电泳筛选患病家族THRB基因的异常情况,结果也有力地支持了甲状腺激素抵抗是由THRB基因异常引起的这一假设。对甲状腺激素抵抗的分子分析将有助于理解该综合征的病理生理学以及甲状腺激素作用的分子机制。

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