Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial disease.Report as inadecuate




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Reference: Bugiardini, E, Poole, OV, Manole, A et al., (2017). Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial disease. Neurology Genetics, 3 (3), e149.Citable link to this page:

 

Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial disease.

Abstract: ObjectivePathologic ribonuclease H1 (RNase H1) causes aberrant mitochondrial DNA (mtDNA) segregation and is associated with multiple mtDNA deletions. We aimed to determine the prevalence of RNase H1 gene (RNASEH1) mutations among patients with mitochondrial disease and establish clinically meaningful genotype-phenotype correlations. MethodsRNASEH1 was analyzed in patients with (1) multiple deletions/depletion of muscle mtDNA and (2) mendelian progressive external ophthalmoplegia (PEO) with neuropathologic evidence of mitochondrial dysfunction, but no detectable multiple deletions/depletion of muscle mtDNA. Clinicopathologic and molecular evaluation of the newly identified and previously reported patients harboring RNASEH1 mutations was subsequently undertaken.ResultsPathogenic c.424G.A p.Val142Ile RNASEH1 mutations were detected in 3 pedigrees among the 74 probands screened. Given that all 3 families had Indian ancestry, RNASEH1 genetic analysis was undertaken in 50 additional Indian probands with variable clinical presentations associated with multiple mtDNA deletions, but no further RNASEH1 mutations were confirmed. RNASEH1-related mitochondrial disease was characterized by PEO (100%), cerebellar ataxia (57%), and dysphagia (50%). The ataxia neuropathy spectrum phenotype was observed in 1 patient. Although the c.424G.A p.Val142Ile mutation underpins all reported RNASEH1- related mitochondrial disease, haplotype analysis suggested an independent origin, rather than a founder event, for the variant in our families.ConclusionsIn our cohort, RNASEH1 mutations represent the fourth most common cause of adult mendelian PEO associated with multiple mtDNA deletions, following mutations in POLG, RRM2B, and TWNK. RNASEH1 genetic analysis should also be considered in all patients with POLG-negative ataxia neuropathy spectrum. The pathophysiologic mechanisms by which the c.424G.A p.Val142Ile mutation impairs human RNase H1 warrant further investigation.

Publication status:PublishedPeer Review status:Peer reviewedVersion:Publisher's versionDate of acceptance:2017-03-13 Funder: Seventh Framework Programme   Funder: Medical Research Council   Funder: Wellcome Trust   Funder: National Institute for Health Research   Funder: Lily Foundation   Funder: Government of India   Notes:Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Bibliographic Details

Publisher: American Academy of Neurology

Publisher Website: http://www.neurology.org/

Journal: Neurology Geneticssee more from them

Publication Website: http://ng.neurology.org/

Volume: 3

Issue: 3

Issue Date: 2017-05

pages:e149Identifiers

Doi: https://doi.org/10.1212/NXG.0000000000000149

Issn: 2376-7839

Issn: 2376-7839

Uuid: uuid:71e94f15-1d50-46e5-9f4c-4ba43bddb121

Urn: uri:71e94f15-1d50-46e5-9f4c-4ba43bddb121

Pubs-id: pubs:696716 Item Description

Type: journal-article;

Language: eng

Version: Publisher's versionKeywords: Journal Article

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Author: Bugiardini, E - - - Poole, OV - - - Manole, A - - - Pittman, AM - - - Horga, A - - - Hargreaves, I - - - Woodward, CE - - - Sween

Source: https://ora.ox.ac.uk/objects/uuid:71e94f15-1d50-46e5-9f4c-4ba43bddb121



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