Expression of Cre recombinase in pigment cells

被引:41
作者
Guyonneau, L
Rossier, A
Richard, C
Hummler, E
Beermann, F
机构
[1] Swiss Inst Expt Canc Res, CH-1066 Epalinges, Switzerland
[2] Univ Lausanne, Inst Pharmacol & Toxicol, CH-1005 Lausanne, Switzerland
来源
PIGMENT CELL RESEARCH | 2002年 / 15卷 / 04期
关键词
melanoblast; melanocyte; RPE; Dct; tyrosinase; pigment; Transgenic; Cre;
D O I
10.1034/j.1600-0749.2002.02039.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Conditional gene targeting using the Cre/loxP system enables specific deletion of a gene in a tissue of interest. For application of Cre-mediated recombination in pigment cells, Cre expression has to be targeted to pigment cells in transgenic mice. So far, no pigment cell-specific Cre transgenic line has been reported and we present and discuss our first results on use of Cre recombinase in pigment cells. A construct was generated where Cre recombinase is controlled by the promoter of the mouse dopachrome tautomerase (Dct) gene. The construct was functionally tested in vitro and introduced into mice. Following breeding to two reporter mouse strains, we detected Cre recombinase activity in telencephalon, melanoblasts, and retinal pigment epithelium (RPE). Our data demonstrate the feasibility of pigment cell-specific Cre/loxP-mediated recombination.
引用
收藏
页码:305 / 309
页数:5
相关论文
共 29 条
[1]   STRUCTURE OF THE MOUSE TYROSINASE-RELATED PROTEIN-2 DOPACHROME TAUTOMERASE (TYRP2/DCT) GENE AND SEQUENCE OF 2 NOVEL SLATY ALLELES [J].
BUDD, PS ;
JACKSON, IJ .
GENOMICS, 1995, 29 (01) :35-43
[2]   Increased transgene expression by the mouse tyrosinase enhancer is restricted to neural crest-derived pigment cells [J].
Camacho-Hübner, A ;
Beermann, F .
GENESIS, 2001, 29 (04) :180-187
[3]  
Camacho-Hübner A, 2000, GENESIS, V28, P99, DOI 10.1002/1526-968X(200011/12)28:3/4<99::AID-GENE20>3.0.CO
[4]  
2-D
[5]   Variegated expression and delayed retinal pigmentation during development in transgenic mice with a deletion in the locus control region of the tyrosinase gene [J].
Giménez, E ;
Giraldo, P ;
Jeffery, G ;
Montoliu, L .
GENESIS, 2001, 30 (01) :21-25
[6]   INDEPENDENT CONTROL OF IMMUNOGLOBULIN SWITCH RECOMBINATION AT INDIVIDUAL SWITCH REGIONS EVIDENCED THROUGH CRE-IOXP-MEDIATED GENE TARGETING [J].
GU, H ;
ZOU, YR ;
RAJEWSKY, K .
CELL, 1993, 73 (06) :1155-1164
[7]   Transcription factors in melanocyte development: distinct roles for Pax-3 and Mitf [J].
Hornyak, TJ ;
Hayes, DJ ;
Chiu, LY ;
Ziff, EB .
MECHANISMS OF DEVELOPMENT, 2001, 101 (1-2) :47-59
[8]   Conditional gene targeting of the Scnn1a (αENaC) gene locus [J].
Hummler, E ;
Mérillat, AM ;
Rubera, I ;
Rossier, BC ;
Beermann, F .
GENESIS, 2002, 32 (02) :169-172
[9]   Nomenclature for identified pigmentation genes in the mouse [J].
Jordan, S ;
Beermann, F .
PIGMENT CELL RESEARCH, 2000, 13 (02) :70-71
[10]   Conditional alleles in mice: Practical considerations for tissue-specific knockouts [J].
Kwan, KM .
GENESIS, 2002, 32 (02) :49-62