Objective： The aim of our study was to investigate the effects of down-regulation Bmi-1 by RNA interference （RNAi） in T Lymphocytic leukemia Jurkat cells. Methods： Two complementary oligonucleotide strands were sy...Objective： The aim of our study was to investigate the effects of down-regulation Bmi-1 by RNA interference （RNAi） in T Lymphocytic leukemia Jurkat cells. Methods： Two complementary oligonucleotide strands were synthesized based on the siRNA sequence targeting Bmi-1 gene. After annealing, siRNA strands were recombined into the pRNAT- U6.2 vector, and then DNA sequencing was carded out following transformation and amplification. The recombinant was transfected into Jurkat cells with liposomes. Positive colonies were obtained through G418 selection. The mRNA and protein expressions of Bmi-1 were detected by RT-PCR and Western-blot, respectively. Effects of Bmi-1 silence on cell proliferation, cell cycle and cell aging of Jurkat cells were detected by M＇l-r assay, flow cytometry, colony formation assay and SA-β-Gal staining, respectively. Results： The siRNA recombinant targeting Bmi.1 gene was successfully constructed. All three siRNA recombinants could significantly inhibit the expression of Bmi-l. The siRNA targeting 825nt-843nt （GACCAGACCACTACT GAAT） has the strongest inhibitory effect on Bmi-1 expression, with almost complete inhibition on Bmi-1 mRNA and protein expressions. Compared with the non-transfection group and the empty vector group, growth velocity and colony formation ability were significantly decreased, while the proportion of calls in G1 phase and the percentage of senile cells were signifi- cantly increased in highly transfected group （P 〈 0.05）. Conclusion： Down-regulation Bmi-1 by RNA interference （RNAi） could significantly inhibit the growth of Jurkat cells in vitro.展开更多
文摘Objective： The aim of our study was to investigate the effects of down-regulation Bmi-1 by RNA interference （RNAi） in T Lymphocytic leukemia Jurkat cells. Methods： Two complementary oligonucleotide strands were synthesized based on the siRNA sequence targeting Bmi-1 gene. After annealing, siRNA strands were recombined into the pRNAT- U6.2 vector, and then DNA sequencing was carded out following transformation and amplification. The recombinant was transfected into Jurkat cells with liposomes. Positive colonies were obtained through G418 selection. The mRNA and protein expressions of Bmi-1 were detected by RT-PCR and Western-blot, respectively. Effects of Bmi-1 silence on cell proliferation, cell cycle and cell aging of Jurkat cells were detected by M＇l-r assay, flow cytometry, colony formation assay and SA-β-Gal staining, respectively. Results： The siRNA recombinant targeting Bmi.1 gene was successfully constructed. All three siRNA recombinants could significantly inhibit the expression of Bmi-l. The siRNA targeting 825nt-843nt （GACCAGACCACTACT GAAT） has the strongest inhibitory effect on Bmi-1 expression, with almost complete inhibition on Bmi-1 mRNA and protein expressions. Compared with the non-transfection group and the empty vector group, growth velocity and colony formation ability were significantly decreased, while the proportion of calls in G1 phase and the percentage of senile cells were signifi- cantly increased in highly transfected group （P 〈 0.05）. Conclusion： Down-regulation Bmi-1 by RNA interference （RNAi） could significantly inhibit the growth of Jurkat cells in vitro.
