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双侧纹状体坏死及与线粒体ND1基因新的T3308C突变相关的线粒体脑肌病伴乳酸酸中毒及卒中样发作综合征

Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 gene.

作者信息

Campos Y, Martín M A, Rubio J C, Gutiérrez del Olmo M C, Cabello A, Arenas J

机构信息

Centro de Investigación, Hospital Universitario "12 de Octubre,", Madrid, Spain.

出版信息

Biochem Biophys Res Commun. 1997 Sep 18;238(2):323-5. doi: 10.1006/bbrc.1997.7166.

Abstract

We found a novel maternally inherited T3308C mutation in the mtDNA ND1 gene in a patient with bilateral striatal necrosis and stroke-like episodes. Muscle biopsy from the proband showed mitochondrial proliferation in blood vessels and normal respiratory chain activities. The mutation, which was not present in 100 normal controls or in 30 patients with mitochondrial disease, was heteroplasmic in both muscle and blood of the proband and in blood from her asymptomatic mother. This mutation results in a Met --> Thr change at the highly conserved amino acid position 1. The T3308C mutation may alter the hydrophobicity and antigenicity of the N-terminal peptide of ND1.

摘要

我们在一名患有双侧纹状体坏死和类中风发作的患者的线粒体DNA ND1基因中发现了一种新的母系遗传T3308C突变。先证者的肌肉活检显示血管中线粒体增殖以及呼吸链活性正常。该突变在100名正常对照者或30名线粒体疾病患者中均未出现,在先证者的肌肉和血液以及其无症状母亲的血液中均为异质性。此突变导致高度保守的第1位氨基酸处发生甲硫氨酸→苏氨酸的改变。T3308C突变可能会改变ND1 N端肽的疏水性和抗原性。

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