Literature DB >> 7799443

Mitochondrial gene expression during bovine cardiac growth and development.

J Marin-Garcia1, R Ananthakrishnan, N Agrawal, M J Goldenthal.   

Abstract

The expression of both mitochondrial and nuclear genes encoding enzymes involved in electron transport and oxidative phosphorylation was examined in bovine cardiac tissue during early growth, development and aging. The steady state level of mRNAs for mitochondrial genes including ATPase 6. COXII and cyt b increased 2.5-4-fold relative to early fetal levels in late fetal and young adult tissues and showed a marked decline (30-50%) in older adult tissues. Similar results were found with the nuclear genes, COXVB and ATP-beta synthase showing coordinate regulation of the two genomes. An increase in mtDNA copy number correlated with the increase in transcript level. Enzyme activity levels for NADH dehydrogenase and cytochrome c oxidase showed a similar trend, albeit of lesser magnitude. These activity levels contrasted with the activity level of an entirely nuclear-encoded mitochondrial enzyme, citrate synthase, which increased not only throughout development but in the older adult tissue. This study indicates that there is a pattern of increasing mitochondrial and nuclear gene expression for OXPHOS enzymes in developing cardiac tissue and decreasing OXPHOS gene expression in the aging heart.

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Year:  1994        PMID: 7799443     DOI: 10.1006/jmcc.1994.1123

Source DB:  PubMed          Journal:  J Mol Cell Cardiol        ISSN: 0022-2828            Impact factor:   5.000


  6 in total

1.  NADH-O2 oxidoreductase activity and mRNA expression of complex I (51 kDa, ND1) in postnatal intrinsic muscle of rat tongue.

Authors:  Toshiya Fujita; Iwao Sato
Journal:  J Anat       Date:  2003-02       Impact factor: 2.610

2.  Heart mitochondrial DNA and enzyme changes during early human development.

Authors:  J Marin-Garcia; R Ananthakrishnan; M J Goldenthal
Journal:  Mol Cell Biochem       Date:  2000-07       Impact factor: 3.396

3.  Human mitochondrial function during cardiac growth and development.

Authors:  J Marin-Garcia; R Ananthakrishnan; M J Goldenthal
Journal:  Mol Cell Biochem       Date:  1998-02       Impact factor: 3.396

4.  Aldose reductase mediates myocardial ischemia-reperfusion injury in part by opening mitochondrial permeability transition pore.

Authors:  Radha Ananthakrishnan; Michiyo Kaneko; Yuying C Hwang; Nosirudeen Quadri; Teodoro Gomez; Qing Li; Casper Caspersen; Ravichandran Ramasamy
Journal:  Am J Physiol Heart Circ Physiol       Date:  2008-12-05       Impact factor: 4.733

5.  Physical exercise regulates p53 activity targeting SCO2 and increases mitochondrial COX biogenesis in cardiac muscle with age.

Authors:  Zhengtang Qi; Jie He; Yuhui Su; Qiang He; Jingxia Liu; Lu Yu; Omar Al-Attas; Tajamul Hussain; Shuzhe Ding; Liu Ji; Min Qian
Journal:  PLoS One       Date:  2011-07-07       Impact factor: 3.240

6.  Differential Alterations of the Mitochondrial Morphology and Respiratory Chain Complexes during Postnatal Development of the Mouse Lung.

Authors:  Natalia El-Merhie; Eveline Baumgart-Vogt; Adrian Pilatz; Susanne Pfreimer; Bianca Pfeiffer; Oleg Pak; Djuro Kosanovic; Michael Seimetz; Ralph Theo Schermuly; Norbert Weissmann; Srikanth Karnati
Journal:  Oxid Med Cell Longev       Date:  2017-12-19       Impact factor: 6.543

  6 in total

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