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患者的基因型表明不存在父系线粒体DNA贡献。

Genotypes from patients indicate no paternal mitochondrial DNA contribution.

作者信息

Taylor Robert W, McDonnell Martina T, Blakely Emma L, Chinnery Patrick F, Taylor Geoffrey A, Howell Neil, Zeviani Massimo, Briem Egill, Carrara Franco, Turnbull Douglass M

机构信息

School of Neurology, Neurobiology and Psychiatry, The Medical School, University of Newcastle upon Tyne, Newcastle upon Tyne, United Kingdom.

出版信息

Ann Neurol. 2003 Oct;54(4):521-4. doi: 10.1002/ana.10673.

Abstract

A cornerstone of mitochondrial genetics, strict maternal inheritance, has been challenged recently by the study of a patient with mitochondrial myopathy due to a sporadic 2bp deletion. The mitochondrial DNA (mtDNA) harboring the mutation was paternal in origin, whereas the patient's blood was identical to the maternal genotype. To determine whether this is a common phenomenon, we studied mtDNA sequence variation between muscle and blood from 35 patients with sporadic mitochondrial myopathies, but detected no evidence of paternal mtDNA transmission. Our findings suggest that paternal transmission of mtDNA is rare and should not alter our genetic advice to families.

摘要

线粒体遗传学的基石——严格的母系遗传,最近受到了一项针对一名因散发性2bp缺失导致线粒体肌病患者研究的挑战。携带该突变的线粒体DNA(mtDNA)起源于父系,而患者血液中的mtDNA与母系基因型相同。为了确定这是否是一种常见现象,我们研究了35例散发性线粒体肌病患者肌肉和血液之间的mtDNA序列变异,但未发现父系mtDNA传递的证据。我们的研究结果表明,mtDNA的父系传递很少见,不应改变我们对家族的遗传建议。

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