【摘要】 目的:构建可研究Polo样激酶1(Plk1)定位的HeLa细胞系。方法:用PCR方法扩增Plk1基因,定向克隆到pRex-EGFP-IRES-Hygro载体中,构建pRex-EGFP-Plk1-IRES-Hygro表达载体;利用逆转录病毒感染的方法,向HeLa细胞系中依次转染pRex-EGFP-Plk1-IRES-Hygro、pRex-Cherry-H2B-IRES-Hygro,构建Hela/GFP-Plk1/Cherry-H2B稳定细胞系;激光共聚焦显微镜观察Hela/GFP-Plk1/Cherry-H2B稳定细胞系在不同有丝细胞分裂期时Plk1的定位。结果:质粒酶切及测序证明pRex-EGFP-Plk1-IRES-Hygro载体构建正确;在Hela/GFP-Plk1/Cherry-H2B稳定细胞系有丝分裂中期和末期时,观察到Plk1分别定位于着丝粒和中间体上。结论:构建了Hela/GFP-Plk1/CherryH2B稳定细胞系,为研究Plk1在有丝分裂不同时期的调控机制提供了细胞模型。更多还原

【Abstract】 Objective: To construct HeLa cells available for study of localization of Polo-like kinase1(Plk1). Methods: Plk1 gene was amplified by PCR and then inserted into vector pRex-EGFP-IRES-Hygro to construct pRex-EGFP-Plk1-IRES-Hygro plasmid. Through retroviral infection, the pRex-EGFP-Plk1-IRES-Hygro and pRexCherry-H2B-IRES-Hygro plasmids were transfected into HeLa cells in turn to construct HeLa/GFP-Plk1/CherryH2B stable cells. The localization of Plk1 in different mitotic phase was observed under confocal laser scanning microscope. Results: The vector pRex-EGFP-Plk1-IRES-Hygro was verified by enzyme digestion and sequencing. In constructed HeLa/GFP-Plk1/Cherry-H2B stable cells, Plk1 was observed in kinetochores and midbody respectively in metaphase and telophase. Conclusion: The constructed HeLa/GFP-Plk1/Cherry-H2B stable cells will benefit the further research on the regulation mechanism of Plk1 in mitosis.更多还原