国家自然科学基金资助项目(39780014,30300173),细胞增殖及调控生物学教育部重点实验室资助项目.
This work was supported by grants from The National Natural Sciences Foundation of China (39780014,30300173) and The Key Laboratory of Cell Proliferation and Regulation Biology of Ministry of Education.
P15RS 是在 p15INK4b 高表达的人黑色素瘤细胞 MLIK6 G1 期中发现和克隆的新基因 . 研究表明,该基因可能在 G1 期作为增殖负调因子起作用 . 为了观察 P15RS 基因产物在细胞中的定位,构建了表达 P15RS-EGFP 融合蛋白的真核表达质粒 pEGFP-P15RS. 用绿色荧光蛋白 GFP 作为报告基因,以人胃癌细胞 BGC-823 为实验模型,将 pEGFP-P15RS 转染 BGC-823 细胞 . 实验表明, P15RS 基因表达产物在 G1 期、 S 期和 G2 期均定位于细胞核内,未见在核仁中分布, M 期凝缩的染色体上未见 . 因此, P15RS 可能定位在核质中 .
P15RS was identified as a novel gene cloned from the human melanoma cell model MLIK6 overexpressing p15INK4b. P15RS has been reported as a negative regulator of cell proliferation in G1 phase. To investigate the localization of P15RS, EGFP-P15RS, a fusion protein with EGFP reporter was constructed and overexpressed in BGC-823 cells. The results showed that EGFP-P15RS protein was distributed in nuclear in interphase (G1, S, G2 phase) of BGC-823 cells. The EGFP-P15RS protein was observed not to localize in chromosome in M phase, suggesting that P15RS might be located in karyoplasm.
张小勇,张 伟,高 萍,常智杰,孙一娜,柳惠图.新基因 P15RS 表达产物在人胃癌细胞细胞周期中定位的研究[J].生物化学与生物物理进展,2005,32(8):771-776
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