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Distribution of T-DNA carrying a Ds element on rice chromosomes
作者姓名:WANG Jiang  LI Lin  WAN Xinshan  AN Linsheng & ZHANG Jingliu National Key Laboratory of Plant Molecular Genetics  Institute of Plant Physiology & Ecology  Shanghai Institutes for Biological Sciences  Chinese Academy of Sciences  Shanghai  China
作者单位:WANG Jiang,LI Lin,WAN Xinshan,AN Linsheng & ZHANG Jingliu National Key Laboratory of Plant Molecular Genetics,Institute of Plant Physiology & Ecology,Shanghai Institutes for Biological Sciences,Chinese Academy of Sciences,Shanghai 200032,China
摘    要:Rice is one of the most important crops in the world, and is widely studied as a model for cereal ge-nomics because of its small genome size (about 430 Mbp), and its colinearity at the sequence level with limited regions of other cereal genomes. In addition, there are a large number of rice databases document-ing molecular markers, genome sequences, EST se-quences and trait mutants1—4]. Functional genomic studies of rice are increasing with the availability of the complete genome sequence. …


Distribution of T-DNA carrying a Ds element on rice chromosomes
WANG Jiang,LI Lin,WAN Xinshan,AN Linsheng & ZHANG Jingliu National Key Laboratory of Plant Molecular Genetics,Institute of Plant Physiology & Ecology,Shanghai Institutes for Biological Sciences,Chinese Academy of Sciences,Shanghai ,China.Distribution of T-DNA carrying a Ds element on rice chromosomes[J].Science China Life sciences,2004,47(4):322-331.
Authors:Wang Jiang  Li Lin  Wan Xinshan  An Linsheng and Zhang Jingliu
Institution:National Key Laboratory of Plant Molecular Genetics, Institute of Plant Physiology & Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China.
Abstract:Over 3000 rice plants with T-DNA carrying a Ds element were constructed by Agro-bacterium tumefaciens mediation. Using inverse PCR methodology, 590 unique right flanking sequences of T-DNA (Ds) were retrieved from independent transformants and classified into six main types on the basis of the origin of filler DNA between the right border of T-DNA and flanking sequence of rice genome. Type I sequences were the most common and showed canonical in-tegration that T-DNA right border was followed by rice genome sequence with or without filler DNA of no more than 50 bp, while type II sequences displayed a vector-genome combination that T-DNA right border was followed by a vector fragment and then connected with rice genome sequence. The location and distribution of 340 type I and II flanking sequences on the rice chromosome were determined using BLAST analysis. The 340 Ds insertions at an average in-terval of 0.8 megabase (Mb) constructed a basic framework of Ds starter points on whole rice chromosomes. The frequency of T-DNA (Ds) inserted into the exons of predicted genes on chromosome one was 21%. Knowledge of T-DNA (Ds) locations on chromosomes will prove to be a useful resource for isolating rice genes by Ds transposon tagging as these Ds insertions can be used as starting lines for further mutagenesis.
Keywords:Ds element  T-DNA  mutagenesis  rice (Oryza sativa L  )    
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