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作 者:刘洋[1] 徐宇[1] 张芙蓉[1] 谭灿 杨国玲[1] Liu Yang;Xu Yu;Zhang Furong;Tan Can;Yang Guoling(Department of Dermatology,The First Affiliated Hospital of Dalian Medical University,Dalian 116011,China)
机构地区:[1]大连医科大学附属第一医院皮肤科,116011
出 处:《中华皮肤科杂志》2019年第3期189-192,共4页Chinese Journal of Dermatology
基 金:国家自然科学基金(81071330).
摘 要:目的用增强型绿色荧光蛋白(EGFP)标记犬小孢子菌PQ-LRP蛋白,明确PQ-LRP蛋白在犬小孢子菌中的定位。方法提取犬小孢子菌总RNA,反转录为cDNA作为模板,PCR扩增PQLRP基因,将PQ-LRP基因与EGFP基因构成融合基因,连接到pCAMBIA 1300质粒载体.采用根癌农杆菌转化法对犬小孢子菌进行转化,使融合基因LRP-EGFP在真菌通用启动子(Ptrpc)和终止子(Ttrpc)调控下在犬小孢子菌中整合型表达,激光共聚焦显微镜检测融合蛋白的细胞定位。结果成功构建表达载体pCAMBIA-LRP-EGFP,融合基因LRP-EGFP在犬小孢子菌中获得整合型表达。激光共聚焦显微镜下LRP-EGFP的荧光信号呈颗粒状或团块状集中于犬小孢子菌的细胞膜上。结论LRP-EGFP融合基因在犬小孢子菌中成功表达,且PQ-LRP蛋白定位于犬小孢子菌细胞膜上。Objective To determine the location of PQ-LRP protein in Microsporum canis using the enhanced green fluorescent protein (EGFP) as a marker. Methods The total RNA was extracted from Microsporum canis, and reversely transcribed into cDNA. The PQ-LRP gene was amplified by PCR using the above cDNA as the template. The fusion gene of PQ-LRP gene and EGFP gene was linked to the plasmid pCAMBIA 1300. Microsporum canis was subjected to Agrobacterium tumefaciens-mediated transformation, in order to achieve the integrated expression of the fusion gene LRP-EGFP in Microsporum canis under the regulation by the fungal universal promoter Ptrpc and terminator Ttrpc. Laser-scanning confocal microscopy was conducted to determine the cellular localization of the fusion protein. Results The expression vector pCAMBIA - LRP - EGFP was successfully constructed, and the fusion gene LRP - EGFP was expressed integratedly in Microsporum canis. Laser-scanning confocal microscopy showed that fluorescence signals of LRP-EGFP were concentrated on the cell membrane of Microsporum canis, giving a granular or cluster-like appearance. Conclusion The infusion gene LRP - EGFP can be successfully expressed in Microsporum canis, and PQ-LRP protein is located on the cell membrane of Microsporum canis.
关 键 词:小孢子菌属 定位标记 绿色荧光蛋白质类 犬小孢子菌 PQ-LRP 蛋白定位
分 类 号:R379[医药卫生—病原生物学]
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