人类Ca(2+) 感应受体基因的突变会导致家族性低性高血症和新生儿严重的甲状腺功能障碍症
M R Pollak1, E M Brown, Y H Chou
1Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts 02115.
Cell
|December 31, 1993
概括
感应受体基因的突变会导致家族性低性高血症 (FHH) 和新生儿严重甲状腺功能障碍症 (NSHPT). 这种受体对于维持平衡至关重要,缺陷导致水平发生变化.
科学领域:
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
- 内分泌学 在内分泌学.
背景情况:
- 家族性低性高血症 (FHH) 和新生儿严重甲状腺功能障碍 (NSHPT) 是影响平衡的遗传性疾病.
- 感应受体 (CaSR) 是一种与G蛋白结合的受体,参与调节细胞外水平.
研究的目的:
- 研究CaSR基因突变在引起FHH和NSHPT中的作用.
- 描述CaSR突变对受体活性的功能后果.
主要方法:
- 在受影响个体中识别和测序CaSR基因突变.
- 在Xenopus laevis卵细胞中表达野生型和突变的CaSR.
- 电生理学记录以评估受体对多价的反应.
主要成果:
- 在患有FHH和NSHPT的患者中,在CaSR基因中发现了三种非保守的误解突变.
- 突变的CaSR与野生类型受体相比,对多价值的反应显著减弱.
- 这些突变位于CaSR.的细胞外N端域和细胞内循环中.
结论:
- 在CaSR基因中的突变是导致FHH和NSHPT的原因.
- 该CaSR在设定细胞外水平方面发挥着至关重要的作用.
- 缺陷的CaSR功能导致受影响个体的平衡受损.
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