The Tol2kit:: A multisite Gateway-based construction kit for Tol2 transposon transgenesis constructs

被引:1299
作者
Kwan, Kristen M.
Fujimoto, Esther
Grabher, Clemens
Mangum, Benjamin D.
Hardy, Melissa E.
Campbell, Douglas S.
Parant, John M.
Yost, H. Joseph
Kanki, John P.
Chien, Chi-Bin
机构
[1] Univ Utah, Med Ctr, Dept Neurobiol & Anat, MREB 401, Salt Lake City, UT 84132 USA
[2] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
[3] Univ Utah, Dept Oncol Sci, Salt Lake City, UT USA
[4] Univ Utah, Inst Brain, Salt Lake City, UT USA
关键词
transposon; EGFP; mCherry; EMCV IRES; bicistronic; nuclear localization signal;
D O I
10.1002/dvdy.21343
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Transgenesis is an important tool for assessing gene function. In zebrafish, transgenesis has suffered from three problems: the labor of building complex expression constructs using conventional subcloning; low transgenesis efficiency, leading to mosaicism in transient transgenics and infrequent germline incorporation; and difficulty in identifying germline integrations unless using a fluorescent marker transgene. The Tol2kit system uses site-specific recombination-based cloning (multisite Gateway technology) to allow quick, modular assembly of [promoter]-[coding sequence]-[3' tag] constructs in a Tol2 transposon backbone. It includes a destination vector with a cmlc2:EGFP (enhanced green fluorescent protein) transgenesis marker and a variety of widely useful entry clones, including hsp70 and beta-actin promoters; cytoplasmic, nuclear, and membrane-localized fluorescent proteins; and internal ribosome entry sequence-driven EGFP cassettes for bicistronic expression. The Tol2kit greatly facilitates zebrafish transgenesis, simplifies the sharing of clones, and enables large-scale projects testing the functions of libraries of regulatory or coding sequences.
引用
收藏
页码:3088 / 3099
页数:12
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