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Melanocyte‐lineage expression of Cre recombinase using Mitf regulatory elements
Author(s) -
Alizadeh Azita,
Fitch Karen R.,
Niswender Colleen M.,
McKnight G. Stanley,
Barsh Gregory S.
Publication year - 2008
Publication title -
pigment cell and melanoma research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.618
H-Index - 105
eISSN - 1755-148X
pISSN - 1755-1471
DOI - 10.1111/j.1755-148x.2007.00425.x
Subject(s) - microphthalmia associated transcription factor , cre recombinase , melanocyte , biology , transgene , recombinase , melanocortin 1 receptor , genetically modified mouse , genetics , gene , bacterial artificial chromosome , microbiology and biotechnology , allele , transcription factor , melanoma , genome , recombination
Summary Manipulation of gene expression in melanocytes is an important tool for studying pigment cell biology. We constructed transgenic mice in which Cre recombinase was placed under the control of regulatory elements from the Microphthalmia ‐ associated transcriptional factor ( Mitf ) gene using bacterial artificial chromosome (BAC). Bacterial artificial chromosome that contained either 50 or 108 kb DNA 5′ to the melanocyte‐specific (1M) transcriptional start site gave rise to transgenic lines in which Cre is expressed specifically in cells of the melanocyte lineage, as judged by activation of the Gt(Rosa)26 tm1Sor ( R26R ) reporter locus. Activation of R26R is first detectable in melanoblasts of midgestation embryos, and completely marks all melanocyte components of the skin in postnatal animals. To test the utility of the MitfCre transgene, we used a loxP‐targeted allele of the protein kinase A alpha catalytic subunit ( Prkaca ), modified such that Cre‐mediated recombination activates PKA signaling. On an agouti background, animals carrying both the MitfCre transgene and the targeted Prkaca allele ( CαR ) exhibited a darker coat color than control littermates, due to a shift from pheomelanin to eumelanin synthesis. Our results confirm that PKA signaling is a key component of pigment type‐switching, and provide a new tool for studying pigment cell biology.