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发根农杆菌依赖的胡椒(Capsicum annuum)叶片外植体转化根的生产:一种用于基因功能分析的新的有效工具。

Agrobacterium rhizogenes-dependent production of transformed roots from foliar explants of pepper (Capsicum annuum): a new and efficient tool for functional analysis of genes.

机构信息

INRA Avignon, UR 1052, Unité de Génétique et Amélioration des Fruits et Légumes, BP 94, 84143, Montfavet Cedex, France,

出版信息

Plant Cell Rep. 2012 Feb;31(2):391-401. doi: 10.1007/s00299-011-1174-z. Epub 2011 Oct 21.

DOI:10.1007/s00299-011-1174-z
PMID:22016085
Abstract

Pepper is known to be a recalcitrant species to genetic transformation via Agrobacterium tumefaciens. A. rhizogenes-mediated transformation offers an alternative and rapid possibility to study gene functions in roots. In our study, we developed a new and efficient system for A. rhizogenes transformation of the cultivated species Capsicum annuum. Hypocotyls and foliar organs (true leaves and cotyledons) of Yolo Wonder (YW) and Criollo de Morelos 334 (CM334) pepper cultivars were inoculated with the two constructs pBIN-gus and pHKN29-gfp of A. rhizogenes strain A4RS. Foliar explants of both pepper genotypes infected by A4RS-pBIN-gus or A4RS-pHKN29-gfp produced transformed roots. Optimal results were obtained using the combination of the foliar explants with A4RS-pHKN29-gfp. 20.5% of YW foliar explants and 14.6% of CM334 foliar explants inoculated with A4RS-pHKN29-gfp produced at least one root expressing uniform green fluorescent protein. We confirmed by polymerase chain reaction the presence of the rolB and gfp genes in the co-transformed roots ensuring that they integrated both the T-DNA from the Ri plasmid and the reporter gene. We also demonstrated that co-transformed roots of YW and CM334 displayed the same resistance response to Phytophthora capsici than the corresponding untransformed roots. Our novel procedure to produce C. annuum hairy roots will thus support the functional analysis of potential resistance genes involved in pepper P. capsici interaction.

摘要

胡椒被认为是一种难以通过根癌农杆菌进行遗传转化的顽固物种。发根农杆菌介导的转化为研究根部基因功能提供了一种替代和快速的可能性。在我们的研究中,我们开发了一种新的、有效的 A. rhizogenes 转化栽培辣椒品种的方法。Yolo Wonder(YW)和 Criollo de Morelos 334(CM334)辣椒品种的下胚轴和叶器官(真叶和子叶)被 A. rhizogenes 菌株 A4RS 的两个构建体 pBIN-gus 和 pHKN29-gfp 接种。被 A4RS-pBIN-gus 或 A4RS-pHKN29-gfp 感染的两种辣椒基因型的叶外植体都产生了转化的根。使用 A4RS-pHKN29-gfp 结合叶外植体可获得最佳结果。YW 叶外植体中有 20.5%,CM334 叶外植体中有 14.6%接种 A4RS-pHKN29-gfp 后至少产生一条表达均匀绿色荧光蛋白的根。我们通过聚合酶链反应证实了 rolB 和 gfp 基因存在于共转化的根中,这确保了它们整合了 Ri 质粒的 T-DNA 和报告基因。我们还证明,YW 和 CM334 的共转化根对辣椒疫霉的抗性反应与相应的未转化根相同。我们生产 C. annuum 发根的新程序将支持参与辣椒 P. capsici 相互作用的潜在抗性基因的功能分析。

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