Derangement of a factor upstream of RARalpha triggers the repression of a pleiotropic epigenetic network.

Francesca Corlazzoli, Stefano Rossetti, Gaia Bistulfi, Mingqiang Ren, Nicoletta Sacchi

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

BACKGROUND: Chromatin adapts and responds to extrinsic and intrinsic cues. We hypothesize that inheritable aberrant chromatin states in cancer and aging are caused by genetic/environmental factors. In previous studies we demonstrated that either genetic mutations, or loss, of retinoic acid receptor alpha (RARalpha), can impair the integration of the retinoic acid (RA) signal at the chromatin of RA-responsive genes downstream of RARalpha, and can lead to aberrant repressive chromatin states marked by epigenetic modifications. In this study we tested whether the mere interference with the availability of RA signal at RARalpha, in cells with an otherwise functional RARalpha, can also induce epigenetic repression at RA-responsive genes downstream of RARalpha. METHODOLOGY/PRINCIPAL FINDINGS: To hamper the availability of RA at RARalpha in untransformed human mammary epithelial cells, we targeted the cellular RA-binding protein 2 (CRABP2), which transports RA from the cytoplasm onto the nuclear RARs. Stable ectopic expression of a CRABP2 mutant unable to enter the nucleus, as well as stable knock down of endogenous CRABP2, led to the coordinated transcriptional repression of a few RA-responsive genes downstream of RARalpha. The chromatin at these genes acquired an exacerbated repressed state, or state "of no return". This aberrant state is unresponsive to RA, and therefore differs from the physiologically repressed, yet "poised" state, which is responsive to RA. Consistent with development of homozygosis for epigenetically repressed loci, a significant proportion of cells with a defective CRABP2-mediated RA transport developed heritable phenotypes indicative of loss of function. CONCLUSION/SIGNIFICANCE: Derangement/lack of a critical factor necessary for RARalpha function induces epigenetic repression of a RA-regulated gene network downstream of RARalpha, with major pleiotropic biological outcomes.

Original languageEnglish (US)
JournalPLoS One
Volume4
Issue number1
StatePublished - Jan 1 2009

Fingerprint

Retinoic Acid Receptors
retinoic acid
Tretinoin
Epigenomics
epigenetics
receptors
Chromatin
Genes
Epigenetic Repression
Carrier Proteins
chromatin
binding proteins
Retinoic Acid Receptor alpha
Availability
Gene Regulatory Networks
Cues
genes
Cytoplasm
Breast
Aging of materials

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Agricultural and Biological Sciences(all)

Cite this

Corlazzoli, F., Rossetti, S., Bistulfi, G., Ren, M., & Sacchi, N. (2009). Derangement of a factor upstream of RARalpha triggers the repression of a pleiotropic epigenetic network. PLoS One, 4(1).

Derangement of a factor upstream of RARalpha triggers the repression of a pleiotropic epigenetic network. / Corlazzoli, Francesca; Rossetti, Stefano; Bistulfi, Gaia; Ren, Mingqiang; Sacchi, Nicoletta.

In: PLoS One, Vol. 4, No. 1, 01.01.2009.

Research output: Contribution to journalArticle

Corlazzoli, F, Rossetti, S, Bistulfi, G, Ren, M & Sacchi, N 2009, 'Derangement of a factor upstream of RARalpha triggers the repression of a pleiotropic epigenetic network.', PLoS One, vol. 4, no. 1.
Corlazzoli, Francesca ; Rossetti, Stefano ; Bistulfi, Gaia ; Ren, Mingqiang ; Sacchi, Nicoletta. / Derangement of a factor upstream of RARalpha triggers the repression of a pleiotropic epigenetic network. In: PLoS One. 2009 ; Vol. 4, No. 1.
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