国家自然科学基金资助项目(39970172, 30540079, 30670449)和中国科学院上海生命科学研究院创新基金资助项目
This work was supported by grants from The National Natural Science Foundation of China (39970172, 30540079, 30670449) and The Creation Foundation of Shanghai Institutes for Biological Sciences, The Chinese Academy of Sciences
CCAAT/增强子结合蛋白β(C/EBPβ) mRNA的3′非翻译区(3′UTR),是先前工作发现的一个具有肿瘤抑制功能的RNA调控元件.应用基因定点突变技术将该3′UTR cDNA上的三段核苷酸同时缺失掉,将缺失突变体稳定转染人肝癌细胞系SMMC-7721,并检测了该缺失突变体对SMMC-7721细胞系表型的影响,包括测定稳转细胞系的生长曲线、软琼脂集落形成能力、细胞集落形成能力及裸小鼠成瘤性.研究发现,C/EBPβ 3′UTR中这三段短序列的同时缺失明显降低了3′UTR的肿瘤抑制活性,使受其稳定转染的细胞系恶性显著增强.人全基因组基因芯片分析和实时荧光RT-PCR分析结果表明,与回复对照细胞相比,缺失突变3′UTR稳定转染细胞中,一些癌基因的表达量有所增加,而一些抑癌基因的表达量有所下降,这提示上述三段短序列是C/EBPβ 3′UTR的肿瘤抑制功能所同时需要的.
The 3′untranslated region of CCAAT/enhancer binding protein β(C/EBPβ) is a regulation element with tumor suppression activity found in previous study. Here, it is reported that deletion of 3 short sequences in this 3′UTR reduces the tumor suppression activity of it, as demonstrated by slowed-down cell growth, reduced colony formation ability in soft agar and in ordinary culture conditions, as well as the decreased tumorigenicity in nude mice. The cDNA array and real-time RT-PCR analysis showed that the loss of tumor suppression activity for the mutated 3′UTR was due to the change of the gene expression profile of the transfected cells, i.e. the up-regulation of several genes related with malignant phenotype and the down-regulation of some genes related with tumor suppression, compared with the revertant control cells. These results indicate that those short sequences are simultaneous necessary for the tumor suppression activity of the C/EBPβ 3′UTR.
王海震,王 莹,孙达权,刘定干. C/EBPβ mRNA 3′非翻译区肿瘤抑制功能的分子机制——同时缺失3段短序列降低其肿瘤抑制活性[J].生物化学与生物物理进展,2009,36(9):1134-1140
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