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机构地区:[1]东北师范大学遗传与细胞研究所
出 处:《实验生物学报》2005年第5期369-376,共8页Acta Biologiae Experimentalis Sinica
基 金:国家"973"重点基础研究计划(G1999053902)国家自然科学基金资助项目(30370316)基金河南师范大学青年基金(20040012)
摘 要:从HeLa细胞中分离的人的Elongator复合物在组成及与RNAPⅡ的作用方式上与酵母的E- longator复合物十分相似,但对其功能研究极少。为了研究人的Elongator复合物催化亚基Elp3的功能,将人elp3等基因转入酵母elp3基因缺失的突变菌株(elp3Δ菌株),并对转化菌株进行功能互补实验和ssa3和pho5基因表达分析,结果表明人elp3基因可显著恢复突变菌株对高温和Caffeine的敏感性,在低磷条件下显著补偿了突变株pho5基因表达延迟的缺陷,并可在热激条件下提高ssa3基因的表达。含酵母elp3非HAT区和人elp3 HAT区的融合yhelp3对上述缺陷有着更强的补偿能力。而HAT区催化结构域缺失的yhelp3HAT没有任何补偿能力,表明人Elp3亚基可能与酵母的该亚基功能相似,人Elp3的HAT活性也为其行使功能所必需。The human elongator complex was found to be very similar to the yeast Elongator both in composition and its interaction with RNA polymerase Ⅱ. But little is known about its functions in vivo. In this study, we analyzed the functions of the help3, the catalytic subunit of human Elongator, using a yeast complementation system. The results indicated that help3 was able to significantly complement the growth defects of the elp3 a yeast strain under high temperature and caffeine conditions. Gene expression analysis showed that help3 significantly resumed the slow activation of the pho5 gene under the low phosphate condition, and when heat shocked it increased the expression level of ssa3 gene. The yhelp3 containing the HAT domain of human elp3 and the remainder of yeast elp3 had a higher complementation ability than human elp3, while the yhelp3HA T- with the catalytic HAT domain deleted had no complementation ability. These results implicate that human Elp3 subunit had similar functions to those of the yeast, and the HAT activity of human Elp3 was essential for its function.
关 键 词:elp3基因 HAT活性 Elongator复合物 功能互补 基因缺失 催化亚基 补偿能力 生长缺陷 缺失菌株 复合物
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