| 香蕉枯萎病菌内源报告基因细胞周期蛋白C1基因FocFCC1的鉴定及分析 |
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| 引用本文： | 曾凡云,王艳玮,漆艳香,谢艺贤,张欣,彭军.香蕉枯萎病菌内源报告基因细胞周期蛋白C1基因FocFCC1的鉴定及分析[J].热带作物学报,2021,42(11):3126-3133. |
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| 作者姓名： | 曾凡云 王艳玮 漆艳香 谢艺贤 张欣 彭军 |
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| 作者单位： | 中国热带农业科学院环境与植物保护研究所/农业农村部热带作物有害生物综合治理重点实验室/海南省热带农业有害生物监测与控制重点实验室,海南海口 571101 |
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| 基金项目： | 海南省基础与应用基础研究计划(自然科学领域)高层次人才项目(No. 2019RC269);国家自然科学基金项目(31661143003);财政部和农业农村部国家现代农业产业技术体系专项(CARS-31-07) |
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| 摘 要： | 本研究克隆鉴定了香蕉枯萎病菌4号生理小种（Foc4）的细胞周期蛋白C1（Fusarium Cyclin C1,FCC1）基因FocFCC1,采用Split-marker同源重组技术获得基因敲除突变体ΔFocFCC1,通过比较突变体和野生菌株在生长速度、产孢量和致病力等方面的差异,探索了FocFCC1基因缺失对香蕉枯萎病菌生物学功能的影响,并评估了FocFCC1作为枯萎菌内源报告基因的可行性。结果表明：与Foc4野生型菌株相比,ΔFocFCC1菌丝生长缓慢、菌丝畸形及产孢量减少,对巴西蕉苗的致病力明显减弱,推测FocFCC1基因在Foc4的生长发育、产孢及致病力等方面具有重要作用。以FocFCC1为靶标基因,评估了两种基因敲除重组方法介导的基因敲除效率,利用红色表型作为判断依据,挑取再生板上有红色表型的转化子进行PCR检测,Split-marker重组方法获得阳性转化子比例为91.7%,而多片段装配融合方法获得阳性转化子的比例为64%。ΔFocFCC1出现典型红色菌落,红色表型与PCR检测的FocFCC1阳性敲除转化子一一对应,FocFCC1基因敲除后红色表型肉眼容易分辨,可作为香蕉枯萎病菌内源报告基因探索新的遗传操作技术在该菌上应用的可行性。
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| 关 键 词： | 香蕉枯萎菌 细胞周期蛋白C1 基因敲除 表型分析 致病力 |
| 收稿时间： | 2020-03-08 |
Identification and analysis the endogenous reporter gene of Cyclin C1 gene FocFCC1 in Fusarium oxysporum f. sp. cubense |
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| ZENG Fanyun,WANG Yanwei,QI Yanxiang,XIE Yixian,ZHANG Xin,PENG Jun.Identification and analysis the endogenous reporter gene of Cyclin C1 gene FocFCC1 in Fusarium oxysporum f. sp. cubense[J].Chinese Journal of Tropical Crops,2021,42(11):3126-3133. |
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| Authors: | ZENG Fanyun WANG Yanwei QI Yanxiang XIE Yixian ZHANG Xin PENG Jun |
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| Institution: | Environment and Plant Protection Institute, Chinese Academy of Tropical Agricultural Sciences / Key Laboratory of Integrated Pest Management on Tropical Crops, Ministry of Agriculture and Rural Affairs, China / Hainan Key Laboratory for Monitoring and Control of Tropical Agricultural Pests, Haikou Hainan 571101, China |
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| Abstract: | In this study, the Fusarium Cyclin C1 gene FocFCC1 in F. oxysporum f. sp. cubense race 4 (Foc4) was cloned and identified. The ΔFocFCC1 gene-knockout mutants were obtained by the Split-marker homologous recombination technique. The growth rate, sporulation, pathogenicity were studied to investigate the biological function of FocFCC1 in Foc4. Additionally, we evaluated whether the FocFCC1 could serve as an endogenous reporter gene applied in Foc4. The results demonstrated that ΔFocFCC1 showed slow growth rate, hyphal deformity, decreased conidium production, and significantly reduced pathogenicity to banana (Cavendish, AAA). Therefore, we hypothesized that FocFCC1 gene might play an important role in the growth, sporulation and pathogenicity of Foc4. Further, a comparative study of the efficiency of two different homologous DNA disruption construct methods was carried out, one is Split-marker recombination approach, another termed Multi-fragment assembly by In-fusion cloning, requires only one standard PCR reaction and one fragment assembly reaction. Using the red phenotype as the judging basis, the transformants with red phenotype on the regeneration plate were selected for PCR detection. The results showed the percentage of positive transformants of Split-marker recombination approach was 91.7%, while that of the Multi-fragment assembly by In-Fusion cloning method was 64%. Next, ΔFocFCC1 showed typical red colony distinguished with Foc4, and the red colony phenotypes coupled with the positive PCR amplification bands. It is important that positive transformants can pick up according to the red phenotype by eyes without PCR procedures, and can serve as endogenous reporter gene for further Foc4 molecular biology research. |
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| Keywords: | Fusarium oxysporum f sp cubense Fusarium Cyclin C1 gene knockout phenotype analysis pathogenicity test |
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