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首页> 外文期刊>Acta botanica sinica >Ac/Ds Transposition Activity in Transgenic Rice Population and DNA Flanking Sequence of Ds Insertion Sites
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Ac/Ds Transposition Activity in Transgenic Rice Population and DNA Flanking Sequence of Ds Insertion Sites

机译:转基因水稻群体中的Ac / Ds转座活性和Ds插入位点的DNA侧翼序列

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摘要

The Agrobacterium mediated transgenic rice ( Oryza sativa L.) population with inserts of maize transposon Activator/Dissociation (Ac/Ds) was investigated. DNA sequences flanking the T-DNA were analyzed with inverse PCR. Results showed that 65.4% of the T-DNA was integrated in different locations of rice genome, and some T-DNA flanking sequences were located on certain chromosomes. A number of T-DNA was found to have inserted into protein coding regions. In order to induce transposition of the inserted Ds elements, 354 crosses of Ac x Ds and Ds x Ac were constructed. The excision frequency of Ds element trans-activated by Ac transposase was 22.7% in the F2 populations, and the transposition was confirmed with analyses of DNA sequences flanking the Ds elements, In addition to the transposition due to "cut-paste" mechanism, Ds can replicate itself and integrate into a new locus, and inaccurate excisions were also found. A proportion of DNA segments flanking the Ds elements showed no homologies to sequences published in GenBank, of which two were registered under the accession numbers AF355153 and AF355770. The strategy of using transposon tagging for rice genomics study was discussed.
机译:研究了农杆菌介导的转基因水稻(Oryza sativa L.)群体,其中插入了玉米转座子激活因子/解离因子(Ac / Ds)。用反向PCR分析T-DNA两侧的DNA序列。结果表明65.4%的T-DNA整合在水稻基因组的不同位置,并且某些T-DNA侧翼序列位于某些染色体上。发现许多T-DNA已插入蛋白质编码区。为了诱导插入的Ds元件的转座,构建了354个Ac x Ds和Ds x Ac的杂交。在F2群体中被Ac转座酶反激活的Ds元件的切除频率为22.7%,并且通过分析Ds元件侧翼的DNA序列分析证实了该转座。除了由于“剪切-粘贴”机制引起的转座之外,Ds可以自我复制并整合到新的基因座中,并且还发现了不正确的切除。 Ds元件两侧的一部分DNA片段与GenBank中公布的序列没有同源性,其中两个以登录号AF355153和AF355770注册。讨论了使用转座子标记进行水稻基因组学研究的策略。

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