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苯甲酰胺和4-氨基-1,8-萘二甲酰亚胺处理通过下调端粒酶相关蛋白的表达并抑制培养细胞中端粒酶逆转录酶的聚(ADP-核糖基)化来抑制端粒酶活性。

Benzamide and 4-amino 1,8 naphthalimide treatment inhibit telomerase activity by down-regulating the expression of telomerase associated protein and inhibiting the poly(ADP-ribosyl)ation of telomerase reverse transcriptase in cultured cells.

作者信息

Ghosh Utpal, Bhattacharyya Nitai P

机构信息

Crystallography and Molecular Biology Division, Saha Institute of Nuclear Physics, Calcutta, India.

出版信息

FEBS J. 2005 Aug;272(16):4237-48. doi: 10.1111/j.1742-4658.2005.04837.x.

Abstract

To test the role of poly(ADP-ribose) polymerase on the telomerase activity, we determined the telomerase activity in leukemic cells K562 treated with benzamide and 4-amino 1,8 naphthalimide (NAP), the inhibitors of PARP. We observed that both the agents inhibited telomerase activity in a dose-dependent manner. The doses of benzamide and NAP that inhibited telomerase activity to 50% of untreated control cells were 10.7 +/- 0.6 mm and 200 +/- 7 microm, respectively. Benzamide treatment (10 mm) inhibited telomerase activity in a time-dependent manner. We also tested the ability of benzamide to inhibit the telomerase activity in Chinese hamster V79 cells and observed similar inhibition of the telomerase activity. Expression of telomerase reverse transcriptase (TERT) and telomerase RNA component, detected by RT-PCR, remained unaltered by treatment with benzamide or NAP. On the contrary, the expression of telomerase associated protein (TEP1/TP1), as detected by RT-PCR and western blot analysis, was reduced by both the agents. Further, in K562 cells, immunoprecipitation with the anti-TERT IgG and probed anti-poly (ADP-ribose) IgG revealed that TERT was poly(ADP-ribosyl)ated in the physiological condition of cell growth and such poly(ADP-ribosyl)ation was inhibited by benzamide treatment. Decrease in TEP1/TP1 expression and poly(ADP-ribosyl)ation of TERT were correlated with the inhibition of PARP activity by benzamide, indicating that PARP had a role in telomerase activity through poly(ADP-ribosyl)ation of TERT and down-regulation of TEP1/TP1.

摘要

为了测试聚(ADP - 核糖)聚合酶对端粒酶活性的作用,我们测定了用苯甲酰胺和4 - 氨基 - 1,8 - 萘二甲酰亚胺(NAP)(聚(ADP - 核糖)聚合酶抑制剂)处理的白血病细胞K562中的端粒酶活性。我们观察到这两种试剂均以剂量依赖性方式抑制端粒酶活性。将端粒酶活性抑制至未处理对照细胞50%的苯甲酰胺和NAP剂量分别为10.7±0.6 mM和200±7 μM。苯甲酰胺处理(10 mM)以时间依赖性方式抑制端粒酶活性。我们还测试了苯甲酰胺抑制中国仓鼠V79细胞中端粒酶活性的能力,并观察到对端粒酶活性有类似的抑制作用。通过RT - PCR检测,端粒酶逆转录酶(TERT)和端粒酶RNA组分的表达在用苯甲酰胺或NAP处理后保持不变。相反,通过RT - PCR和蛋白质印迹分析检测,端粒酶相关蛋白(TEP1 / TP1)的表达被这两种试剂降低。此外,在K562细胞中,用抗TERT IgG进行免疫沉淀并用抗聚(ADP - 核糖)IgG进行检测发现,在细胞生长的生理条件下TERT被聚(ADP - 核糖)化,并且这种聚(ADP - 核糖)化被苯甲酰胺处理所抑制。TEP1 / TP1表达的降低和TERT的聚(ADP - 核糖)化与苯甲酰胺对聚(ADP - 核糖)聚合酶活性的抑制相关,表明聚(ADP - 核糖)聚合酶通过TERT的聚(ADP - 核糖)化和TEP1 / TP1的下调在端粒酶活性中发挥作用。

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