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患者出现晚发性夏科-马里-图什病(CMT),髓鞘蛋白零(MPZ)完全缺失。

Complete Loss of Myelin protein zero (MPZ) in a patient with a late onset Charcot-Marie-Tooth (CMT).

机构信息

Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

Department of Orthopedic Surgery, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Metab Brain Dis. 2023 Aug;38(6):1963-1970. doi: 10.1007/s11011-023-01201-x. Epub 2023 Mar 23.

Abstract

Charcot-Marie-Tooth (CMT) comprises a group of hereditary neuropathies with clinical, epidemiological, and molecular heterogeneity in which variants in more than 80 different genes have been reported. One of the important genes which cause 5% of all CMT cases is Myelin protein zero (P0, MPZ). Variants in this gene have been reported in association with different forms of CMT including classical CMT1, severe DSS (CMT3B), DI-CMT, CMT2I and CMT2J with autosomal dominant (AD) inheritance. To our knowledge, MPZ variants have not been described in autosomal recessive (AR) form of CMT in previous studies. Moreover, its complete deletion has not been reported in human. Here, we described clinical characteristics of a patient with CMT symptoms who demonstrated manifestations of the disease late in his life. We performed exome sequencing for identifying CMT subtype and its associated gene, and follow that co-segregation analysis has been done to characterize inheritance pattern of the disorder. Through using exome sequencing, we identified a novel 4074 bp homozygote deletion which encompasses all 6 exons of the MPZ gene in this patient. After identifying the alteration, variant confirmation and co-segregation analysis have been performed by using specific primers. Our result revealed that the patient's parents were heterozygous for the alteration and they did not show any symptoms of CMT. Although most MPZ variants have been described with early onset CMT with AD pattern of inheritance, the reported patient in our study had late onset form and his parents did not show any symptoms. Considering substantial role of MPZ protein in the biogenesis of peripheral nervous system (PNS) myelin, we proposed that there should be another protein in PNS that compensates for lack of MPZ protein. Taken together, our finding is the first report of MPZ association with AR form of CMT with late onset features. Moreover, our results propose the presence of another protein in PNS myelin biogenesis and its assembly. However, functional studies alongside with other molecular studies are needed to confirm our results and identify the proposed protein.

摘要

Charcot-Marie-Tooth (CMT) 包括一组具有临床、流行病学和分子异质性的遗传性神经病,其中已经报道了 80 多种不同基因的变异。导致所有 CMT 病例的 5%的一个重要基因是髓鞘蛋白零 (P0,MPZ)。该基因的变异已与包括经典 CMT1、严重 DSS (CMT3B)、DI-CMT、CMT2I 和 CMT2J 在内的不同形式的 CMT 相关报道,具有常染色体显性 (AD) 遗传。据我们所知,在以前的研究中,MPZ 变异未在常染色体隐性 (AR) 形式的 CMT 中描述。此外,其完全缺失尚未在人类中报道。在这里,我们描述了一位具有 CMT 症状的患者的临床特征,他在生命后期表现出该疾病的症状。我们进行了外显子组测序以确定 CMT 亚型及其相关基因,然后进行共分离分析以描述该疾病的遗传模式。通过使用外显子组测序,我们在该患者中鉴定出一个包含 MPZ 基因的所有 6 个外显子的 4074 bp 纯合缺失。在鉴定出该改变后,使用特定引物进行了变体确认和共分离分析。我们的结果显示,患者的父母为该改变的杂合子,他们没有表现出任何 CMT 症状。尽管大多数 MPZ 变异已被描述为具有 AD 遗传模式的早发性 CMT,但我们研究中的报告患者具有晚发性形式,他的父母没有表现出任何症状。考虑到 MPZ 蛋白在周围神经系统 (PNS) 髓鞘发生中的重要作用,我们提出 PNS 中应该存在另一种蛋白来弥补 MPZ 蛋白的缺乏。总之,我们的发现是第一个报道的与 AR 形式的 CMT 相关的 MPZ 与晚发性特征。此外,我们的结果提出了 PNS 髓鞘发生和组装中另一种蛋白的存在。然而,需要进行功能研究以及其他分子研究来证实我们的结果并确定所提出的蛋白。

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