首页> 美国卫生研究院文献>Plant Physiology >Sequence Analysis of a 282-Kilobase Region Surrounding the Citrus Tristeza Virus Resistance Gene (Ctv) Locus in Poncirus trifoliata L. Raf.
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Sequence Analysis of a 282-Kilobase Region Surrounding the Citrus Tristeza Virus Resistance Gene (Ctv) Locus in Poncirus trifoliata L. Raf.

机译:三角果(Poncirus trifoliata L. Raf)的柑橘Tristeza病毒抗性基因(Ctv)基因座周围的282个碱基的序列分析。

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摘要

Citrus tristeza virus (CTV) is the major virus pathogen causing significant economic damage to citrus worldwide, and a single dominant gene, Ctv, provides broad spectrum resistance to CTV in Poncirus trifoliata L. Raf. Ctv was physically mapped to a 282-kb region using a P. trifoliata bacterial artificial chromosome library. This region was completely sequenced to about 8× coverage using a shotgun sequencing strategy and primer walking for gap closure. Sequence analysis predicts 22 putative genes, two mutator-like transposons and eight retrotransposons. This sequence analysis also revealed some interesting features of this region of the P. trifoliata genome: a disease resistance gene cluster with seven members and eight retrotransposons clustered in a 125-kb gene-poor region. Comparative sequence analysis suggests that six genes in the Ctv region have significant sequence similarity with their orthologs in bacterial artificial chromosome clones F7H2 and F21T11 from Arabidopsis chromosome I. However, the analysis of gene colinearity between P. trifoliata and Arabidopsis indicates that Arabidopsis genome sequence information may be of limited use for positional gene cloning in P. trifoliata and citrus. Analysis of candidate genes for Ctv is also discussed.
机译:柑橘Tristeza病毒(CTV)是导致全世界柑橘遭受重大经济损害的主要病毒病原体,并且一个单一的显性基因Ctv为Trifoliata L. Raf的CTV提供了广谱抗性。使用三叶假单胞菌细菌人工染色体文库将Ctv物理映射到282-kb区域。使用a弹枪测序策略和引物步移封闭间隙,将该区域完全测序至约8x覆盖率。序列分析预测22个推定基因,两个突变体样转座子和八个逆转座子。该序列分析还揭示了三叶假单胞菌基因组区域的一些有趣特征:一个抗病基因簇,该簇具有七个成员和八个逆转座子,聚集在一个125kb的基因贫乏区域。比较序列分析表明,Ctv区中的六个基因与其在拟南芥属染色体I的细菌人工染色体克隆F7H2和F21T11中的直系同源序列具有显着序列同源性。但是,对三叶拟南芥和拟南芥之间的基因共线性分析表明,拟南芥的基因组序列信息三叶假单胞菌和柑橘中的位置基因克隆可能用途有限。还讨论了Ctv候选基因的分析。

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