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[通过限制性片段长度多态性(RFLP)研究分析格雷夫斯病中的促甲状腺激素受体基因结构]

[Analysis of the TSH receptor gene structure in Graves' disease by a restriction fragment length polymorphism (RFLP) study].

作者信息

Monden T, Yamada M, Mori M

机构信息

First Department of Internal Medicine, Gunma University School of Medicine.

出版信息

Nihon Rinsho. 1994 Apr;52(4):1052-6.

PMID:7910860
Abstract

We examined the structure of the TSH receptor gene in thyroid disorders, particularly in Graves' disease by a RFLP study with a cloned human TSH receptor cDNA as a probe. Southern blot analysis indicated that the TSH receptor gene is a single copy gene in the human genome. Although RFLPs were not detected in peripheral blood cells and thyroid tissues in patient with Graves' disease, significant RFLPs were found in 2 of 6 patients with adenoma. We conclude that there are no major abnormalities in the structure of the TSH receptor gene in patients with Graves' disease, and that DNA from thyroid adenomas can have large insertions or deletions.

摘要

我们通过以克隆的人促甲状腺激素(TSH)受体cDNA为探针的限制性片段长度多态性(RFLP)研究,检测了甲状腺疾病,特别是格雷夫斯病中TSH受体基因的结构。Southern印迹分析表明,TSH受体基因在人类基因组中是单拷贝基因。虽然在格雷夫斯病患者的外周血细胞和甲状腺组织中未检测到RFLP,但在6例腺瘤患者中的2例发现了显著的RFLP。我们得出结论,格雷夫斯病患者的TSH受体基因结构没有重大异常,并且甲状腺腺瘤的DNA可能有大的插入或缺失。

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