4.4 Article

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

期刊

DEVELOPMENTAL DYNAMICS
卷 236, 期 11, 页码 3088-3099

出版社

WILEY
DOI: 10.1002/dvdy.21343

关键词

transposon; EGFP; mCherry; EMCV IRES; bicistronic; nuclear localization signal

资金

  1. NCI NIH HHS [2P-01 CA68484-11A1] Funding Source: Medline
  2. NEI NIH HHS [R01 EY12873] Funding Source: Medline
  3. NHLBI NIH HHS [R01 HL66292] Funding Source: Medline
  4. NICHD NIH HHS [5T32 HD07491] Funding Source: Medline

向作者/读者索取更多资源

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.

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