灰葡萄孢菌(Botrytis cinerea)基因组中T-DNA整合模式分析
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浙江省钱江人才计划(2009R10030);浙江省人事厅留学回国人员择优资助项目


Analysis of T-DNA integration pattern in Botrytis cinerea genome
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Supported by the Qianjiang Excellence Project of Zhejiang Province(2009R10030)

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    摘要:

    摘要:【目的】研究灰葡萄孢菌(Botrytis cinerea)基因组中T-DNA插入位点的整合模式特征。【方法】利用农杆菌(Agrobactirium tumfacience)介导法构建灰葡萄孢菌T-DNA插入突变体库。利用热不对称交错PCR(TAIL-PCR)技术对转化子中T-DNA的旁侧序列进行扩增和克隆,对获得的旁侧序列进行比对分析。【结果】T-DNA插入在灰葡萄孢菌基因组非编码区的占69%,插入在外显子的占30%。T-DNA在插入的过程中发生了碱基缺失、增加等重组现象,其中左边界(left border,LB)整合到基因组碱基缺失较少,有的保持完整,而右边界(right border,RB)及其近邻的T-DNA区域缺失碱基较多。T-DNA的插入位点还发现有额外的序列插入。【结论】对灰葡萄孢菌中插入T-DNA的整合模式的分析为开展该菌的功能基因组学奠定了基础。

    Abstract:

    Abstract: [Objective] To analyze the T-DNA integration pattern in the genome of grey mold Botrytis cinerea. [Methods] T-DNA (Transfer DNA) inserted mutant library of Botrytis cinerea was created by Agrobactirium tumfacience mediated transformation. By using TAIL-PCR (Thermal asymmetric interlaced polymerase chain reaction), we amplified and cloned the chromosomal regions flanking T-DNA insertions. The obtained T-DNA flanking sequences were subjected to alignment with standard T-DNA border sequence for identification and analysis of integration. [Results] Up to 69% T-DNA inserted at noncoding regions and 30% inserted at exons. Recombination including deletion or addition of bases in T-DNA region was observed. The right borders of the T-DNA were frequently truncated, and by contrast the left borders were less prone to degradation and appeared to have been inserted in a relatively integrated manner. Extra sequence additions also occurred in T-DNA integration sites. [Conclusion] Analysis of T-DNA integration pattern in B. cinerea genome will stimulate the functional genomics study of this fungus.

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刘佳,张剑云,朱廷恒,汪琨,崔志峰. 灰葡萄孢菌(Botrytis cinerea)基因组中T-DNA整合模式分析. 微生物学报, 2011, 51(2): 203-207

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  • 收稿日期:2010-10-18
  • 最后修改日期:2010-11-17
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