Literature DB >> 18467192

Does strong hypertrophic condition induce fast mitochondrial DNA mutation of rabbit heart?

Taeho Kim1, Vu Thi Thu, Il-Yong Han, Jae Boum Youm, Euiyong Kim, Sun Woo Kang, Yang Wook Kim, Jae Hwa Lee, Hyun Joo.   

Abstract

Homo- and heteroplasmic mitochondrial DNA (mtDNA) mutations were observed and identified in an isoproterenol-induced rabbit model of cardiac hypertrophy. Genes encoding proteins essential for catalyzing mitochondrial electron transfer and for generating the proton motive force, such as NADH dehydrogenases (ND2, ND3, ND4, and ND6), cytochrome b, and ATPase 8, showed increased susceptibility for mutation. Specifically, five mutations caused amino acid changes and were located in Complex I and Complex V gene clusters. To our knowledge, this is the first demonstration of a relationship between cardiac hypertrophy induced by a strong sympathetic load and rapid mtDNA mutations.

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Year:  2008        PMID: 18467192     DOI: 10.1016/j.mito.2008.03.003

Source DB:  PubMed          Journal:  Mitochondrion        ISSN: 1567-7249            Impact factor:   4.160


  2 in total

1.  Cardiac overexpression of 8-oxoguanine DNA glycosylase 1 protects mitochondrial DNA and reduces cardiac fibrosis following transaortic constriction.

Authors:  Jianxun Wang; Qianwen Wang; Lewis J Watson; Steven P Jones; Paul N Epstein
Journal:  Am J Physiol Heart Circ Physiol       Date:  2011-08-26       Impact factor: 4.733

2.  Glutathione peroxidase 1 protects mitochondria against hypoxia/reoxygenation damage in mouse hearts.

Authors:  Vu Thi Thu; Hyoung Kyu Kim; Seung Hee Ha; Ji-Young Yoo; Won Sun Park; Nari Kim; Goo Taeg Oh; Jin Han
Journal:  Pflugers Arch       Date:  2010-03-20       Impact factor: 3.657

  2 in total

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