Regulation of heme oxygenase-1 mRNA deadenylation and turnover in NIH3T3 cells by nitrosative or alkylation stress
2007

How Nitric Oxide Affects Heme Oxygenase-1 mRNA in Cells

publication Evidence: moderate

Author Information

Author(s): Leautaud Veronica, Demple Bruce

Primary Institution: Harvard School of Public Health

Hypothesis

NO treatment stops poly(A) tail shortening at the critical 30- to 50-nt length.

Conclusion

Nitric oxide stabilizes HO-1 mRNA by preventing the final steps of deadenylation, while other stressors have different effects.

Supporting Evidence

  • NO exposure increased the half-life of HO-1 mRNA from ~1.6 h to 11 h.
  • CdCl2, NaAsO2, and H2O2 increased the half-life of HO-1 mRNA only up to 5 h.
  • Methyl methane sulfonate also stabilized HO-1 mRNA but decreased the deadenylation rate.

Takeaway

When cells are stressed, a molecule called nitric oxide helps keep a message (mRNA) that tells the cell to make a protective protein longer, so the cell can better handle the stress.

Methodology

NIH3T3 cells were treated with nitric oxide donors and other stressors, followed by measurement of HO-1 mRNA half-life and deadenylation rates.

Limitations

The study's findings may not apply to all cell types, as some cells did not show the same response to NO.

Statistical Information

P-Value

p<0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/1471-2199-8-116

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