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Post-transcriptional regulation of melanin biosynthetic enzymes by cAMP and resveratrol in human melanocytes


Newton, RL and Cook, AL and Roberts, DW and Leonard, JH and Sturm, RA, Post-transcriptional regulation of melanin biosynthetic enzymes by cAMP and resveratrol in human melanocytes, Journal of Investigative Dermatology, 127, (9) pp. 2216-2227. ISSN 0022-202X (2007) [Refereed Article]

DOI: doi:10.1038/sj.jid.5700840


Upregulation of microphthalmia-associated transcription factor (MITF) expression has been proposed to mediate melanogenesis stimulated by cAMP, whereas downregulation of MITF has been suggested to underlie the depigmentary effects of resveratrol, a promising chemotherapeutic found in red wine. We have assessed the contribution of MITF to pigmentation regulation by treating primary cultures of normal human melanocytes with the adenylate cyclase activator forskolin and/or resveratrol, then quantifying mRNA and protein levels for MITF, tyrosinase, tyrosinase-related protein-1, and dopachrome tautomerase (DCT). The inhibition of tyrosinase activity by resveratrol was not due to alterations in MITF, but instead was explained by both direct tyrosinase inhibition and a post-transcriptional effect that reduced the amount of fully processed tyrosinase. Glycosidase digestion revealed that the basis for the tyrosinase decrease was the retention of an immature form in the ER and subsequent loss of the mature, Golgi-processed enzyme. Elevation of intracellular cAMP by forskolin markedly increased protein levels for MITF, tyrosinase and DCT, however there was no concomitant increase in tyrosinase or DCT mRNA. This indicated that elevated levels of MITF were not sufficient to promote transcription of these melanogenic genes and that the increase in their protein abundance appeared to be predominantly mediated through post-transcriptional processing events.

Item Details

Item Type:Refereed Article
Research Division:Biomedical and Clinical Sciences
Research Group:Oncology and carcinogenesis
Research Field:Cancer genetics
Objective Division:Health
Objective Group:Clinical health
Objective Field:Clinical health not elsewhere classified
UTAS Author:Cook, AL (Associate Professor Tony Cook)
ID Code:68249
Year Published:2007
Web of Science® Times Cited:83
Deposited By:Health Sciences A
Deposited On:2011-03-10
Last Modified:2011-07-29

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