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一个家族中先天性感觉神经性聋和骨髓增生异常综合征存在胚系 GATA2 移码突变导致提前终止密码子。

A novel germline GATA2 frameshift mutation with a premature stop codon in a family with congenital sensory hearing loss and myelodysplastic syndrome.

机构信息

Division of Hematology, Department of Internal Medicine, Shinshu University School of Medicine, 3-1-1, Matsumoto, Nagano, 3908621, Japan.

Center for Medical Genetics, Shinshu University Hospital, Matsumoto, Japan.

出版信息

Int J Hematol. 2021 Aug;114(2):286-291. doi: 10.1007/s12185-021-03130-w. Epub 2021 Mar 23.

Abstract

GATA2 is a zinc-finger transcription factor regulating early hematopoiesis and developmental processes. Heterozygous germline mutations in GATA2 underlie a pleiotropic autosomal dominant disorder, GATA2 deficiency syndrome. The wide spectrum of its clinical features involves familial predisposition to myelodysplastic syndrome (MDS)/acute myeloid leukemia (AML) and multiorgan dysfunction, including congenital sensorineural hearing loss (CSHL). We herein report a pedigree with a novel germline frameshift mutation presenting as CSHL and familial MDS. The proband was a 46-year-old man, and his daughter also presented with an identical set of clinical syndromes. Target DNA sequencing identified a novel eight-nucleotide duplicative insertion at exon 5 (NM_032638.4:c.1126_1133dup:p.Lys378Asnfs*12) of the GATA2 gene. RT-PCR and subcloning analysis showed that the frameshift might result in a truncated mutation with an early stop codon without interfering with the predicted splice site. The predicted mutant protein had 388 amino acids and in silico analysis showed the variant was considered deleterious. This mutation was not detected in unaffected family members. Its deleterious effect is highly likely to have portended the familial MDS and CSHL in this pedigree. Genetic testing among suspected individuals may be warranted for adequate management, including timely transplantation.

摘要

GATA2 是一种锌指转录因子,调节早期造血和发育过程。GATA2 的种系突变杂合子是一种多效性常染色体显性疾病,即 GATA2 缺乏综合征。其广泛的临床特征包括家族性倾向骨髓增生异常综合征(MDS)/急性髓系白血病(AML)和多器官功能障碍,包括先天性感觉神经性耳聋(CSHL)。本文报道了一个具有新型种系移码突变的家系,表现为 CSHL 和家族性 MDS。先证者为 46 岁男性,其女儿也表现出完全相同的一组临床综合征。目标 DNA 测序鉴定出 GATA2 基因外显子 5(NM_032638.4:c.1126_1133dup:p.Lys378Asnfs*12)上的一个新型 8 个核苷酸重复插入,这是一种新型种系移码突变,导致提前出现无义密码子,而不干扰预测的剪接位点。RT-PCR 和亚克隆分析表明,移码可能导致截短突变,并提前出现无义密码子。预测的突变蛋白有 388 个氨基酸,计算机分析显示该变体被认为是有害的。该突变未在未受影响的家庭成员中检测到。这种突变很可能导致了该家系中的家族性 MDS 和 CSHL。对疑似个体进行遗传检测可能是必要的,以进行充分的管理,包括及时移植。

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