De Bonis Maria, De Paolis Elisa, Onori Maria Elisabetta, Mazzuccato Giorgia, Gatto Antonio, Ferrara Pietro, Ferraro Pietro Manuel, Urbani Andrea, Minucci Angelo
UOS Diagnostica Molecolare E Genomica, Fondazione Policlinico Universitario A. Gemelli-IRCCS, Largo Agostino Gemelli, 00168, Rome, Italy.
UOC Pediatria, Dipartimento Scienze della Salute della Donna, del Bambino E Di Sanità Pubblica- Area Salute del Bambino, Fondazione Policlinico Universitario A. Gemelli-IRCCS, Largo Agostino Gemelli, 00168, Rome, Italy.
Mol Biol Rep. 2021 Apr;48(4):3303-3311. doi: 10.1007/s11033-021-06324-x. Epub 2021 Apr 17.
Pathogenic variants (PVs) in CYP24A1 gene are associated with Idiopathic Infantile Hypercalcemia disease (IIH). The identification of CYP24A1 PVs can be a useful tool for the improvement of target therapeutic strategies. Aim of this study is to set up a rapid and inexpensive High Resolution Melting Analysis (HRMA)-based method for the simultaneous genotyping of two hot spot PVs in CYP24A1 gene, involved in IIH. A duplex-HRMA (dHRMA) was designed in order to detect simultaneously CYP24A1 c.428_430delAAG, p.(Glu143del) (rs777676129) and c.1186C > T, p.(Arg396Trp) (rs114368325), in peculiar cases addressed to our Laboratory. dHRMA was able to identify clearly and simultaneously both hot spot CYP24A1 PVs evaluating melting curve shape and melting temperature (T). This is the first dHRMA approach to rapidly screen the two most frequent CYP24A1 PVs in peculiar case, providing useful information for diagnosis and patient management in IIH disease.
CYP24A1基因的致病性变异(PVs)与特发性婴儿高钙血症(IIH)相关。CYP24A1 PVs的鉴定可能是改善靶向治疗策略的有用工具。本研究的目的是建立一种基于高分辨率熔解分析(HRMA)的快速且廉价的方法,用于同时对参与IIH的CYP24A1基因中的两个热点PVs进行基因分型。设计了一种双重HRMA(dHRMA),以便在送交我们实验室的特殊病例中同时检测CYP24A1基因的c.428_430delAAG、p.(Glu143del)(rs777676129)和c.1186C>T、p.(Arg396Trp)(rs114368325)。dHRMA能够通过评估熔解曲线形状和熔解温度(T)清晰且同时地鉴定出两个热点CYP24A1 PVs。这是第一种在特殊病例中快速筛查两个最常见的CYP24A1 PVs的dHRMA方法,为IIH疾病的诊断和患者管理提供了有用信息。