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Expression and knockdown of primordial germ cell genes, vasa, nanos and dead end in common carp (Cyprinus carpio) embryos for transgenic sterilization and …

Aquaculture. 2014; 
BaofengSuaEricPeatmanaMeiShangaRonThresherbPeterGrewebJawaharPatilbCarl A.PinkertcMichael H.IrwincChaoLiaDayan A.PereraaPatricia L.DuncandMichaelFobesaRex A.Dunhama
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Gene Synthesis The catfish nanos promoter was used to drive the tet-off system. Other promoters included the adenylosuccinate synthase (ADSS) promoter and the racemase promoter (RM) from zebrafish, the copper transport protein (CTR3) from the yeast Saccharomyces cerevisiae (abbreviation M), and the CTR3 promoter but less sensitive (removed the first 869 bp from CTR3 promoter (CTR3-237) (abbreviation MCTR). After designing the constructs, they were synthesized at GenScript Corporation (Piscataway, New Jersey, USA). Get A Quote

摘要

Common carp, Cyprinus carpio, is one of the most widely grown aquaculture species. Four types of knock-down constructs designed to transgenically sterilize fish were electroporated into common carp embryos to knockdown or eliminate expression of primordial germ cell (PGC) proteins, nanos or dead end. Embryos from different developmental stages were collected and tested using quantitative real-time PCR. Relative levels of gene expression were compared among control embryos and embryos exposed to these constructs during development. Two proteins, nanos and dead end, were targeted, each specific for a set of constructs, and a third related, but non-targeted PGC protein, vasa, was assayed. The effectiveness... More

关键词

Transient assayTransgenic sterilizationCommon carpReal-time PCR