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Transcriptional Regulation of SDHa flavoprotein by nuclear respiratory factor-1 prevents pseudo-hypoxia in aerobic cardiac cells.

Publication ,  Journal Article
Piantadosi, CA; Suliman, HB
Published in: J Biol Chem
April 18, 2008

Nuclear respiratory factor-1 (NRF-1) is integral to the transcriptional regulation of mitochondrial biogenesis, but its control over various respiratory genes overlaps other regulatory elements including those involved in O(2) sensing. Aerobic metabolism generally suppresses hypoxia-sensitive genes, e.g. via hypoxia-inducible factor-1 (HIF-1), but mutations in Complex II-succinate dehydrogenase (SDH), a tumor suppressor, stabilize HIF-1, producing pseudo-hypoxia. In aerobic cardiomyocytes, which rely on oxidative phosphorylation, we tested the hypothesis that NRF-1 regulates Complex II expression and opposes hypoxia-inducible factor-1. NRF-1 gene silencing blocked aerobic succinate oxidation, increasing nuclear HIF-1alpha protein prior to the loss of Complex I function. We postulated that NRF-1 suppression either specifically decreases the expression of one or more SDH subunits and increases succinate availability to regulate HIF-1 prolyl hydroxylases, or stimulates mitochondrial reactive oxygen production, which interferes with HIF-1alpha degradation. Using promoter analysis, gene silencing, and chromatin immunoprecipitation, NRF-1 was found to bind to the gene promoters of two of four nuclear-encoded Complex II subunits: SDHa and SDHd, but the enzyme activity was dynamically regulated through the catalytic SDHa flavoprotein. Complex II was inactivated by SDHa silencing, which led to aerobic HIF-1alpha stabilization, nuclear translocation, and enhanced expression of glucose transporters and heme oxygenase-1. This was unrelated to mitochondrial ROS production, reversible by high alpha-ketoglutarate concentrations, and coherent with regulation of HIF-1 by succinate reported in tumor cells. These findings disclose a novel role for NRF-1 in the transcriptional control of Complex II and prevention of pseudo-hypoxic gene expression in aerobic cardiac cells.

Duke Scholars

Published In

J Biol Chem

DOI

ISSN

0021-9258

Publication Date

April 18, 2008

Volume

283

Issue

16

Start / End Page

10967 / 10977

Location

United States

Related Subject Headings

  • Transcription, Genetic
  • Succinate Dehydrogenase
  • Reactive Oxygen Species
  • Rats
  • Nuclear Respiratory Factor 1
  • Molecular Sequence Data
  • Models, Biological
  • Mitochondria
  • Hypoxia
  • Glucose
 

Citation

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Piantadosi, C. A., & Suliman, H. B. (2008). Transcriptional Regulation of SDHa flavoprotein by nuclear respiratory factor-1 prevents pseudo-hypoxia in aerobic cardiac cells. J Biol Chem, 283(16), 10967–10977. https://doi.org/10.1074/jbc.M709741200
Piantadosi, Claude A., and Hagir B. Suliman. “Transcriptional Regulation of SDHa flavoprotein by nuclear respiratory factor-1 prevents pseudo-hypoxia in aerobic cardiac cells.J Biol Chem 283, no. 16 (April 18, 2008): 10967–77. https://doi.org/10.1074/jbc.M709741200.
Piantadosi, Claude A., and Hagir B. Suliman. “Transcriptional Regulation of SDHa flavoprotein by nuclear respiratory factor-1 prevents pseudo-hypoxia in aerobic cardiac cells.J Biol Chem, vol. 283, no. 16, Apr. 2008, pp. 10967–77. Pubmed, doi:10.1074/jbc.M709741200.

Published In

J Biol Chem

DOI

ISSN

0021-9258

Publication Date

April 18, 2008

Volume

283

Issue

16

Start / End Page

10967 / 10977

Location

United States

Related Subject Headings

  • Transcription, Genetic
  • Succinate Dehydrogenase
  • Reactive Oxygen Species
  • Rats
  • Nuclear Respiratory Factor 1
  • Molecular Sequence Data
  • Models, Biological
  • Mitochondria
  • Hypoxia
  • Glucose