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Structural and Functional Complexity of the Genomic Region Controlling AK-Toxin Biosynthesis and Pathogenicity in the Japanese Pear Pathotype of Alternaria alternata

机译:结构和功能复杂的基因组区域控制AK毒素生物合成和致病性的日本梨病原体。

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The Japanese pear pathotype of Alternaria alternata produces host-specific AK-toxin and causes black spot of Japanese pear. Previously, a cosmid clone, pcAKT-1, was isolated that contains two genes, AKT1 and AKT2 , within a 5.0-kb region required for AK-toxin biosynthesis. The wild-type strain has multiple, nonfunctional copies of these genes. In the present study, two additional genes, AKTR-1 and AKT3-1 , downstream of AKT2 were identified. Transformation of the wild type with AKTR-1 - and AKT3-1 -targeting vectors produced toxin-deficient (Toxˉ), nonpathogenic mutants. DNA gel blot analysis, however, demonstrated that the fragments targeted in Toxˉ mutants were different from those containing AKTR-1 and AKT3-1 on the transforming vectors. A cosmid clone, pcAKT-2, containing the targeted DNA was isolated and shown to carry two genes, AKTR-2 and AKT3-2 , with high similarity to AKTR-1 and AKT3-1 , respectively. Transcripts from not only AKTR-2 and AKT3-2 but also AKTR-1 and AKT3-1 were found in the wild type. DNA gel blot analysis with pulsed-field gel electrophoresis showed that AKT1, AKT2, AKT3 , and AKTR and their homologues are on a single chromosome. These results indicate the structural and functional complexity of the genomic region controlling AK-toxin biosynthesis.
机译:交链孢霉的日本梨致病型产生宿主特异性的AK毒素,并引起日本梨黑斑。以前,分离出粘粒克隆pcAKT-1,它在AK毒素生物合成所需的5.0 kb区域内包含两个基因AKT1和AKT2。野生型菌株具有这些基因的多个非功能性拷贝。在本研究中,确定了AKT2下游的另外两个基因AKTR-1和AKT3-1。用AKTR-1和AKT3-1靶向载体转化野生型产生了毒素缺乏(Toxˉ),非致病性突变体。然而,DNA凝胶印迹分析表明,在Tox 1突变体中靶向的片段不同于在转化载体上含有AKTR-1和AKT3-1的片段。分离出含有目标DNA的粘粒克隆pcAKT-2,并显示其携带两个基因AKTR-2和AKT3-2,分别与AKTR-1和AKT3-1具有高度相似性。在野生型中不仅发现了AKTR-2和AKT3-2的转录本,还发现了AKTR-1和AKT3-1的转录本。用脉冲场凝胶电泳进行的DNA凝胶印迹分析表明AKT1,AKT2,AKT3和AKTR及其同源物在一条染色体上。这些结果表明控制AK毒素生物合成的基因组区域的结构和功能复杂性。

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