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作 者:Jilong Chen Jie Liu Yulian Zhang Zhiwei Chen Zhenhua Jin
机构地区:[1]Chinese Acad Sci, Inst Dev Biol, Beijing 100080, Peoples R China
出 处:《Chinese Science Bulletin》2000年第5期456-460,共5页
摘 要:Both FRT-FRT and LoxP-LoxP sites that are the target sepuences of site-specific recombinases have been constructed in a vector, called C4LFY, using the recombinant DNA technigue. C4LFY also contains P elements, 2 exons and 1 intron of Drosophila yellow gene, yellow promoter and enhancers, and flanking DNA. Since C4LFY made use of two pairs of FRT and LoxP sites, this vector included two site-specific recombination systems. C4LFY was then integrated into Drosophila genome by P-element-mediated germ line transformation. in the presence of the FLP or Cre recombinase, either FLP/FRT or Cre/LoxP recombination reaction was successfully created at the same position in the genome. Using this system, the molecular basis of yellow gene expression and regulation during development have been investigated. Results indicate that the tissue-specific expression of yellow gene is directly regulated by transcriptional enhancers. in addition, the 5’ and 3’ genomic sequences flanking the yellow gene have beenBoth FRT-FRT and LoxP-LoxP sites that are the target sequences of site-specific recombinases have been constructed in a vector, called C4LFY, using the recombinant DNA technique. C4LFY also contains P elements, 2 exons and 1 intron of Drosophilayellow gene,yellow promoter and enhancers, and flanking DNA. Since C4LFY made use of two pairs of FRT and LoxP sites, this vector included two site-specific recombination systems. C4LFY was then integrated into Drosophila genome by P-element-mediated germ line transformation. In the presence of the FLP or Cre recombinase, either FLP/FRT or Cre/LoxP recombination reaction was successfully created at the same position in the genome. Using this system, the molecular basis ofyellow gene expression and regulation during development have been investigated. Results indicate that the tissue-specific expression ofyellow gene is directly regulated by transcriptional enhancers. In addition, the 5′ and 3′ genomic sequences flanking theyellow gene have been preliminarily studied and their potential role is discussed.
关 键 词:SITE-SPECIFIC recombination TRANSGENE gene expression and regulation cis-acting elements.
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