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作 者:杨展[1] 赵家明[1] 王旭光[1] 吴平[1] 何惠娟[1] 杨勤[2]
机构地区:[1]广东医学院附属医院中心实验室,广东湛江524001 [2]广东医学院附属医院血液研究室,广东湛江524001
出 处:《第四军医大学学报》2008年第9期792-795,共4页Journal of the Fourth Military Medical University
基 金:广东省卫生厅科研项目(A2006489)
摘 要:目的:探讨c-myc脱氧核酶的切割作用及对白血病细胞端粒酶活性的影响.方法:合成针对c-myc mRNA的“10~23”型脱氧核酶DzMycI及其类似物DzMycI提取总RNA在细胞外切割c-myc mRNA;转染白血病细胞系HL-60后,用RT-PCR扩增c-myc基因片段和端粒酶蛋白亚基hTERT的片段,用PCR-ELISA法测定端粒酶活性.结果:脱氧核酶DzMycI在细胞外和细胞内均能够有效地切割c-myc mRNA;在转染HL-60后,DzMycI显著抑制白血病细胞生长(P〈0.05),下调端粒酶蛋白亚基hTERT的表达,显著降低HL-60细胞端粒酶活性(P〈0.05).DzMycI催化中心的一个碱基被替换后形成的脱氧寡核苷酸DzMycI在胞外和胞内均不表现对c-myc mRNA的切割作用.结论:脱氧核酶DzMycI确实能够高效特异地切割c-myc mRNA,降低白血病细胞端粒酶活性,抑制白血病细胞生长,有可能作为c-myc抑制剂用于白血病的基因治疗领域中.AIM: To explore the cleavage of c-myc mRNA by a DNAzyme and its effect on telomerase activity in a hmnan leukemia cell line HL-60. METHODS: A "10-23" DNAzyme( DzMycI) targeted against c-myc mRNA and its analogues (DzMycI') were synthesized and used to cleave c-myc mRNA. The cleaving efficiency and the expression of human telomerase reverse transcriptase (hTERT) was assessed by RT-PCR and telomerase activity was assayed by PCR-ELISA. RESULTS: DzMycI exhibited effective cleaving ability and after transfection into HL-60 cells, down-regulated the hTERT expression and telomerase activity ( P 〈 0.01 ), and inhibited the growth of the cells ( P 〈 0.05 ). DzMycI', which was derived from DzMycI with a base displacement in the conserved catalytic motif, did not exhibit notable clea- ving effect on c-myc mRNA either outside the cells or in cells. CONCLUSION: The synthesized DNAzyme DzMycI can cleave c-myc mRNA with effectiveness and specificity, decrease the telomerase activity and induce the apoptosis of HL-60 cells. As newly found c-myc inhibitors, DNAzymes will probably play an important role in the gene therapy of leukemia.
关 键 词:催化性DNA 原癌基因蛋白质C-MYC 端粒酶 白血病
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