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SV - 40大T抗原对细胞生长、p34cdc2和细胞周期蛋白A水平的调节

Modulation of cell growth, p34cdc2 and cyclin A levels by SV-40 large T antigen.

作者信息

Oshima J, Steinmann K E, Campisi J, Schlegel R

机构信息

Division of Cell and Molecular Biology, Lawrence Berkeley Laboratory, Berkeley, California 94720.

出版信息

Oncogene. 1993 Nov;8(11):2987-93.

PMID:8414501
Abstract

Immortalization of rat lung epithelial cells by either wild-type SV-40 T antigen, a mutant form of T antigen that cannot bind pRb, or a temperature-sensitive T antigen increased by five- to 20-fold the steady state levels of p34cdc2 and cyclin A, positive regulators of progression through the cell cycle. Increased abundance of p34cdc2 was not accompanied by equivalent increases in cdc2 mRNA, indicating that increased expression of p34cdc2 is due, at least partially, to post-transcriptional mechanisms. Levels of p34cdc2 and cyclin A protein in cells immortalized with a temperature-sensitive T antigen remained elevated at the restrictive temperature unless T antigen was reduced to levels significantly below those where proliferation ceased, indicating that these two functions can be dissociated. These results show that SV-40 T antigen can dramatically enhance the expression of certain cell cycle regulatory proteins by mechanisms that are independent of pRb binding and cell growth status.

摘要

野生型SV - 40 T抗原、无法结合pRb的T抗原突变形式或温度敏感型T抗原使大鼠肺上皮细胞永生化,使细胞周期进程的阳性调节因子p34cdc2和细胞周期蛋白A的稳态水平提高了5至20倍。p34cdc2丰度的增加并未伴随着cdc2 mRNA的等量增加,这表明p34cdc2表达的增加至少部分归因于转录后机制。在用温度敏感型T抗原永生化的细胞中,除非T抗原降低到显著低于增殖停止时的水平,否则在限制温度下p34cdc2和细胞周期蛋白A的蛋白质水平仍会升高,这表明这两种功能可以分离。这些结果表明,SV - 40 T抗原可通过独立于pRb结合和细胞生长状态的机制显著增强某些细胞周期调节蛋白的表达。

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