| Literature DB >> 22119795 |
Maik Hüttemann1, Scott Klewer, Icksoo Lee, Alena Pecinova, Petr Pecina, Jenney Liu, Michael Lee, Jeffrey W Doan, Douglas Larson, Elise Slack, Bita Maghsoodi, Robert P Erickson, Lawrence I Grossman.
Abstract
Subunit 7a of mouse cytochrome c oxidase (Cox) displays a contractile muscle-specific isoform, Cox7a1, that is the major cardiac form. To gain insight into the role of this isoform, we have produced a new knockout mouse line that lacks Cox7a1. We show that homozygous and heterozygous Cox7a1 knockout mice, although viable, have reduced Cox activity and develop a dilated cardiomyopathy at 6 weeks of age. Surprisingly, the cardiomyopathy improves and stabilizes by 6 months of age. Cox7a1 knockout mice incorporate more of the "liver-type" isoform Cox7a2 into the cardiac Cox holoenzyme and, also surprisingly, have higher tissue ATP levels. Copyright ÂEntities:
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Year: 2011 PMID: 22119795 PMCID: PMC3299818 DOI: 10.1016/j.mito.2011.11.002
Source DB: PubMed Journal: Mitochondrion ISSN: 1567-7249 Impact factor: 4.160