Genetic variation in regulatory DNA elements: The case of OCA2 transcriptional regulation
Pigment Cell & Melanoma Research , Volume 27 - Issue 2 p. 169- 177
Mutations within the OCA2 gene or the complete absence of the OCA2 protein leads to oculocutaneous albinism type 2. The OCA2 protein plays a central role in melanosome biogenesis, and it is a strong determinant of the eumelanin content in melanocytes. Transcript levels of the OCA2 gene are strongly correlated with pigmentation intensities. Recent studies demonstrated that the transcriptional level of OCA2 is to a large extent determined by the noncoding SNP rs12913832 located 21.5 kb upstream of the OCA2 gene promoter. In this review, we discuss current hypotheses and the available data on the mechanism of OCA2 transcriptional regulation and how this is influenced by genetic variation. Finally, we will explore how future epigenetic studies can be used to advance our insight into the functional biology that connects genetic variation to human pigmentation.
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|Pigment Cell & Melanoma Research|
|Organisation||Erasmus MC: University Medical Center Rotterdam|
Visser, M, Kayser, M.H, Grosveld, F.G, & Palstra, R.-J.T.S. (2014). Genetic variation in regulatory DNA elements: The case of OCA2 transcriptional regulation. Pigment Cell & Melanoma Research, 27(2), 169–177. doi:10.1111/pcmr.12210