Academic Endocrine Unit, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Nuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.
J Bone Miner Res. 2023 Jun;38(6):907-917. doi: 10.1002/jbmr.4803. Epub 2023 Apr 18.
Familial hypocalciuric hypercalcemia type 2 (FHH2) and autosomal dominant hypocalcemia type 2 (ADH2) are due to loss- and gain-of-function mutations, respectively, of the GNA11 gene that encodes the G protein subunit Gα11, a signaling partner of the calcium-sensing receptor (CaSR). To date, four probands with FHH2-associated Gα11 mutations and eight probands with ADH2-associated Gα11 mutations have been reported. In a 10-year period, we identified 37 different germline GNA11 variants in >1200 probands referred for investigation of genetic causes for hypercalcemia or hypocalcemia, comprising 14 synonymous, 12 noncoding, and 11 nonsynonymous variants. The synonymous and noncoding variants were predicted to be benign or likely benign by in silico analysis, with 5 and 3, respectively, occurring in both hypercalcemic and hypocalcemic individuals. Nine of the nonsynonymous variants (Thr54Met, Arg60His, Arg60Leu, Gly66Ser, Arg149His, Arg181Gln, Phe220Ser, Val340Met, Phe341Leu) identified in 13 probands have been reported to be FHH2- or ADH2-causing. Of the remaining nonsynonymous variants, Ala65Thr was predicted to be benign, and Met87Val, identified in a hypercalcemic individual, was predicted to be of uncertain significance. Three-dimensional homology modeling of the Val87 variant suggested it was likely benign, and expression of Val87 variant and wild-type Met87 Gα11 in CaSR-expressing HEK293 cells revealed no differences in intracellular calcium responses to alterations in extracellular calcium concentrations, consistent with Val87 being a benign polymorphism. Two noncoding region variants, a 40bp-5'UTR deletion and a 15bp-intronic deletion, identified only in hypercalcemic individuals, were associated with decreased luciferase expression in vitro but no alterations in GNA11 mRNA or Gα11 protein levels in cells from the patient and no abnormality in splicing of the GNA11 mRNA, respectively, confirming them to be benign polymorphisms. Thus, this study identified likely disease-causing GNA11 variants in <1% of probands with hypercalcemia or hypocalcemia and highlights the occurrence of GNA11 rare variants that are benign polymorphisms. © 2023 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).
家族性低钙血症性高钙血症 2 型(FHH2)和常染色体显性低钙血症 2 型(ADH2)分别是由于 GNA11 基因突变导致的功能丧失和获得性功能异常,该基因编码 G 蛋白亚基 Gα11,是钙敏感受体(CaSR)的信号伴侣。迄今为止,已经报道了 4 例与 FHH2 相关的 Gα11 突变患者和 8 例与 ADH2 相关的 Gα11 突变患者。在 10 年期间,我们在 >1200 名因高钙血症或低钙血症而接受遗传原因调查的患者中发现了 37 种不同的种系 GNA11 变体,包括 14 种同义、12 种非编码和 11 种非同义变体。通过计算机分析预测,同义和非编码变体为良性或可能良性,其中 5 种和 3 种分别存在于高钙血症和低钙血症患者中。在 13 名患者中发现的 9 种非同义变体(Thr54Met、Arg60His、Arg60Leu、Gly66Ser、Arg149His、Arg181Gln、Phe220Ser、Val340Met、Phe341Leu)已被报道与 FHH2 或 ADH2 相关。其余的非同义变体中,Ala65Thr 被预测为良性,而在高钙血症患者中发现的 Met87Val 被预测为意义不明。Val87 变体的三维同源建模表明它可能是良性的,并且在表达 CaSR 的 HEK293 细胞中表达 Val87 变体和野生型 Met87 Gα11 后,发现细胞内钙对细胞外钙浓度变化的反应没有差异,这与 Val87 是良性多态性一致。仅在高钙血症患者中发现的一个 40bp-5'UTR 缺失和一个 15bp 内含子缺失的两个非编码区变体与体外荧光素酶表达降低有关,但患者细胞中的 GNA11 mRNA 或 Gα11 蛋白水平没有改变,GNA11 mRNA 的剪接也没有异常,分别证实它们是良性多态性。因此,本研究在 <1%的高钙血症或低钙血症患者中发现了可能导致疾病的 GNA11 变体,并强调了 GNA11 罕见变体是良性多态性的发生。© 2023 作者。《骨矿盐研究杂志》由 Wiley 期刊出版公司代表美国骨矿盐研究协会(ASBMR)出版。