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线粒体呼吸复合物 I 遗传异常与神经发育障碍的关系及其临床意义分析。

Genetic aberration analysis of mitochondrial respiratory complex I implications in the development of neurological disorders and their clinical significance.

机构信息

Central Molecular Laboratory, Govind Ballabh Pant Institute of Postgraduate Medical Education and Research (GIPMER), New Delhi 110002, India.

Department of Biochemistry, Govind Ballabh Pant Institute of Postgraduate Medical Education and Research (GIPMER), New Delhi 110002, India.

出版信息

Ageing Res Rev. 2023 Jun;87:101906. doi: 10.1016/j.arr.2023.101906. Epub 2023 Mar 9.

Abstract

Growing neurological diseases pose difficult challenges for modern medicine to diagnose and manage them effectively. Many neurological disorders mainly occur due to genetic alteration in genes encoding mitochondrial proteins. Moreover, mitochondrial genes exhibit a higher rate of mutation due to the generation of Reactive oxygen species (ROS) during oxidative phosphorylation operating in their vicinity. Among the different complexes of Electron transport chain (ETC), NADH: Ubiquinone oxidoreductase (Mitochondrial complex I) is the most important. This multimeric enzyme, composed of 44 subunits, is encoded by both nuclear and mitochondrial genes. It often exhibits mutations resulting in development of various neurological diseases. The most prominent diseases include leigh syndrome (LS), leber hereditary optic neuropathy (LHON), mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS), myoclonic epilepsy associated with ragged-red fibers (MERRF), idiopathic Parkinson's disease (PD) and, Alzheimer's disease (AD). Preliminary data suggest that mitochondrial complex I subunit genes mutated are frequently of nuclear origin; however, most of the mtDNA gene encoding subunits are also primarily involved. In this review, we have discussed the genetic origins of neurological disorders involving mitochondrial complex I and signified recent approaches to unravel the diagnostic and therapeutic potentials and their management.

摘要

不断增长的神经退行性疾病对现代医学提出了严峻挑战,使其难以有效诊断和治疗。许多神经退行性疾病主要是由于编码线粒体蛋白的基因突变引起的。此外,由于附近氧化磷酸化过程中活性氧(ROS)的产生,线粒体基因的突变率更高。在电子传递链(ETC)的不同复合物中,烟酰胺腺嘌呤二核苷酸:泛醌氧化还原酶(线粒体复合物 I)最为重要。这种由 44 个亚基组成的多聚酶,由核基因和线粒体基因共同编码。它经常表现出突变,导致各种神经退行性疾病的发生。最突出的疾病包括 Leigh 综合征(LS)、Leber 遗传性视神经病变(LHON)、伴有乳酸酸中毒和中风样发作的线粒体脑肌病(MELAS)、伴破碎红纤维的肌阵挛性癫痫(MERRF)、特发性帕金森病(PD)和阿尔茨海默病(AD)。初步数据表明,突变的线粒体复合物 I 亚基基因通常来源于核基因;然而,大多数编码亚基的 mtDNA 基因也主要参与其中。在这篇综述中,我们讨论了涉及线粒体复合物 I 的神经退行性疾病的遗传起源,并强调了最近用于揭示其诊断和治疗潜力及其管理的方法。

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