Department of Hematology and Oncology, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatric Metabolismand Inflammatory Diseases, Children's Hospital of Chongqing Medical University, 136 Zhongshanerlu, Yu Zhong district, Chongqing, 400014, China.
Chongqing Key Laboratory of Structural Birth Defect and Reconstruction, Chongqing, China.
BMC Med Genomics. 2024 Aug 12;17(1):206. doi: 10.1186/s12920-024-01973-w.
Hereditary spherocytosis (HS, MIM#612641) is one of the most common hereditary hemolytic disorders. This study aimed to confirm a novel variant's pathogenicity and reveal a patient's genetic etiology.
The clinical data of a patient with HS who underwent genetic sequencing at the Children's Hospital of Chongqing Medical University were reviewed retrospectively. In silico prediction and in vitro minigene splicing reporter system were then conducted on the detected variant to analyze its intramolecular impact. A summary of the literature related to HS due to SPTB gene variants was also presented.
A novel variant (c.301-2 A > G) in the SPTB gene (NM_001024858.4) was identified in the proband. Using Sanger sequencing, we conclusively confirmed that the inheritance of the variant could not be traced to the biological parents. The in vitro minigene assay revealed three different transcripts derived from the c.301-2 A > G variant: r.301_474del, r.301_306delCCAAAG, and r.301-1_301-57ins. Through a literature review, patients with HS who had been genotypically validated were summarized and the SPTB gene variant profile was mapped.
We identified a splicing variant of the SPTB gene, thus confirming its aberrant translation. The novel variant was the probable genetic etiology of the proband with HS. Our findings expanded the variant spectrum of the SPTB gene, thus improving the understanding of the associated hereditary hemolytic disorders from a clinical and molecular perspective and contributing to the foundation of genetic counseling and diagnosis.
遗传性球形红细胞增多症(HS,MIM#612641)是最常见的遗传性溶血性疾病之一。本研究旨在确认一种新变异的致病性,并揭示患者的遗传病因。
回顾性分析重庆医科大学儿童医院接受基因测序的 HS 患者的临床数据。然后对检测到的变异进行计算机预测和体外小基因拼接报告基因系统分析,以研究其对分子的影响。还对 SPTB 基因突变导致 HS 的相关文献进行了总结。
在该先证者的 SPTB 基因(NM_001024858.4)中发现了一个新的变异(c.301-2 A>G)。通过 Sanger 测序,我们明确证实该变异的遗传不能追溯到生物父母。体外小基因实验显示,该变异产生了三种不同的转录本:r.301_474del、r.301_306delCCAAAG 和 r.301-1_301-57ins。通过文献回顾,总结了经过基因分型验证的 HS 患者,并绘制了 SPTB 基因变异图谱。
我们鉴定了 SPTB 基因的剪接变异体,从而证实其翻译异常。该新变异可能是 HS 先证者的遗传病因。我们的发现扩展了 SPTB 基因的变异谱,从而从临床和分子角度提高了对相关遗传性溶血性疾病的认识,并为遗传咨询和诊断奠定了基础。