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Whole mitochondrial genome sequencing of Malaysian patients with cardiomyopathy

Cardiomyopathy (CMP) constitutes a diverse group of myocardium diseases affecting the pumping ability of the heart. Genetic predisposition is among the major factors affecting the development of CMP. Globally, there are over 100 genes in autosomal and mitochondrial DNA (mtDNA) that have been reporte...

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Autores principales: Kuan, Sheh Wen, Chua, Kek Heng, Tan, E-Wei, Tan, Lay Koon, Loch, Alexander, Kee, Boon Pin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013480/
https://www.ncbi.nlm.nih.gov/pubmed/35441061
http://dx.doi.org/10.7717/peerj.13265
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author Kuan, Sheh Wen
Chua, Kek Heng
Tan, E-Wei
Tan, Lay Koon
Loch, Alexander
Kee, Boon Pin
author_facet Kuan, Sheh Wen
Chua, Kek Heng
Tan, E-Wei
Tan, Lay Koon
Loch, Alexander
Kee, Boon Pin
author_sort Kuan, Sheh Wen
collection PubMed
description Cardiomyopathy (CMP) constitutes a diverse group of myocardium diseases affecting the pumping ability of the heart. Genetic predisposition is among the major factors affecting the development of CMP. Globally, there are over 100 genes in autosomal and mitochondrial DNA (mtDNA) that have been reported to be associated with the pathogenesis of CMP. However, most of the genetic studies have been conducted in Western countries, with limited data being available for the Asian population. Therefore, this study aims to investigate the mutation spectrum in the mitochondrial genome of 145 CMP patients in Malaysia. Long-range PCR was employed to amplify the entire mtDNA, and whole mitochondrial genome sequencing was conducted on the MiSeq platform. Raw data was quality checked, mapped, and aligned to the revised Cambridge Reference Sequence (rCRS). Variants were named, annotated, and filtered. The sequencing revealed 1,077 variants, including 18 novel and 17 CMP and/or mitochondrial disease-associated variants after filtering. In-silico predictions suggested that three of the novel variants (m.8573G>C, m.11916T>A and m.11918T>G) in this study are potentially pathogenic. Two confirmed pathogenic variants (m.1555A>G and m.11778G>A) were also found in the CMP patients. The findings of this study shed light on the distribution of mitochondrial mutations in Malaysian CMP patients. Further functional studies are required to elucidate the role of these variants in the development of CMP.
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spelling pubmed-90134802022-04-18 Whole mitochondrial genome sequencing of Malaysian patients with cardiomyopathy Kuan, Sheh Wen Chua, Kek Heng Tan, E-Wei Tan, Lay Koon Loch, Alexander Kee, Boon Pin PeerJ Genomics Cardiomyopathy (CMP) constitutes a diverse group of myocardium diseases affecting the pumping ability of the heart. Genetic predisposition is among the major factors affecting the development of CMP. Globally, there are over 100 genes in autosomal and mitochondrial DNA (mtDNA) that have been reported to be associated with the pathogenesis of CMP. However, most of the genetic studies have been conducted in Western countries, with limited data being available for the Asian population. Therefore, this study aims to investigate the mutation spectrum in the mitochondrial genome of 145 CMP patients in Malaysia. Long-range PCR was employed to amplify the entire mtDNA, and whole mitochondrial genome sequencing was conducted on the MiSeq platform. Raw data was quality checked, mapped, and aligned to the revised Cambridge Reference Sequence (rCRS). Variants were named, annotated, and filtered. The sequencing revealed 1,077 variants, including 18 novel and 17 CMP and/or mitochondrial disease-associated variants after filtering. In-silico predictions suggested that three of the novel variants (m.8573G>C, m.11916T>A and m.11918T>G) in this study are potentially pathogenic. Two confirmed pathogenic variants (m.1555A>G and m.11778G>A) were also found in the CMP patients. The findings of this study shed light on the distribution of mitochondrial mutations in Malaysian CMP patients. Further functional studies are required to elucidate the role of these variants in the development of CMP. PeerJ Inc. 2022-04-14 /pmc/articles/PMC9013480/ /pubmed/35441061 http://dx.doi.org/10.7717/peerj.13265 Text en © 2022 Kuan et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Genomics
Kuan, Sheh Wen
Chua, Kek Heng
Tan, E-Wei
Tan, Lay Koon
Loch, Alexander
Kee, Boon Pin
Whole mitochondrial genome sequencing of Malaysian patients with cardiomyopathy
title Whole mitochondrial genome sequencing of Malaysian patients with cardiomyopathy
title_full Whole mitochondrial genome sequencing of Malaysian patients with cardiomyopathy
title_fullStr Whole mitochondrial genome sequencing of Malaysian patients with cardiomyopathy
title_full_unstemmed Whole mitochondrial genome sequencing of Malaysian patients with cardiomyopathy
title_short Whole mitochondrial genome sequencing of Malaysian patients with cardiomyopathy
title_sort whole mitochondrial genome sequencing of malaysian patients with cardiomyopathy
topic Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013480/
https://www.ncbi.nlm.nih.gov/pubmed/35441061
http://dx.doi.org/10.7717/peerj.13265
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