G-TRACE: rapid Gal4-based cell lineage analysis in Drosophila

被引:253
作者
Evans, Cory J. [1 ]
Olson, John M. [1 ]
Ngo, Kathy T. [1 ]
Kim, Eunha [1 ]
Lee, Noemi E. [1 ]
Kuoy, Edward [1 ]
Patananan, Alexander N. [1 ]
Sitz, Daniel [1 ]
Tran, PhuongThao [1 ]
Do, Minh-Tu [1 ]
Yackle, Kevin [1 ]
Cespedes, Albert [1 ]
Hartenstein, Volker [1 ,2 ,3 ]
Call, Gerald B. [1 ]
Banerjee, Utpal [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Los Angeles, Dept Mol Cell & Dev Biol, Los Angeles, CA 90024 USA
[2] Univ Calif Los Angeles, Dept Biol Chem, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90024 USA
[4] Univ Calif Los Angeles, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell, Los Angeles, CA USA
基金
美国国家卫生研究院;
关键词
EXPRESSION; HEMATOPOIESIS; PROTEIN; EYE;
D O I
10.1038/nmeth.1356
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We combined Gal4-UAS and the FLP recombinase-FRT and fluorescent reporters to generate cell clones that provide spatial, temporal and genetic information about the origins of individual cells in Drosophila melanogaster. We named this combination the Gal4 technique for real-time and clonal expression (G-TRACE). The approach should allow for screening and the identification of real-time and lineage-traced expression patterns on a genomic scale.
引用
收藏
页码:603 / U70
页数:4
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