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Cre‐mediated recombination in the skin melanocyte lineage
Author(s) -
Delmas Véronique,
Martinozzi Silvia,
Bourgeois Yveline,
Holzenberger Martin,
Larue Lionel
Publication year - 2003
Publication title -
genesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.093
H-Index - 110
eISSN - 1526-968X
pISSN - 1526-954X
DOI - 10.1002/gene.10197
Subject(s) - cre recombinase , melanocyte , biology , transgene , genetically modified mouse , cre lox recombination , gene targeting , microbiology and biotechnology , recombinase , reporter gene , gene , phenotype , gene expression , genetics , recombination , melanoma
Summary: Organ‐specific expression of a Cre recombinase allows the analysis of gene function in a particular tissue or cell type. Using a 6.1 kb promoter from the mouse tyrosinase gene, we generated and characterized two lines of transgenic mice that express Cre recombinase in melanoblasts. Utilizing a Cre ‐responsive reporter mouse strain, genetic recombination was detected in the melanoblasts of the skin from embryonic day 11.5. In addition, Cre‐expression was detected in the skin and eyes of mice. Cre transgene activity was occasionally detected in the brain and peripheral nerves but not in other tissues. When Tyr::Cre mice were crossed with mice carrying a homozygous loxP conditional mutation for the insulin‐like growth factor receptor gene ( Igf1r ), Cre‐melanoblast‐specific recombination pattern was confirmed and no abnormal phenotype was observed. In conclusion, Tyr::Cre transgenic mice provide a valuable tool to follow the cell lineage and to examine gene function in melanocyte development and transformation. genesis 36:73–80, 2003. © 2003 Wiley‐Liss, Inc.