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p53导致细胞在G2/M期出现第二个细胞周期阻滞的证据。

Evidence for a second cell cycle block at G2/M by p53.

作者信息

Stewart N, Hicks G G, Paraskevas F, Mowat M

机构信息

Manitoba Institute of Cell Biology, Manitoba Cancer Treatment and Research Foundation, Winnipeg, Canada.

出版信息

Oncogene. 1995 Jan 5;10(1):109-15.

PMID:7529916
Abstract

Wild type p53 can induce cell cycle arrest at specific points in the cell cycle, in particular G1/S, an ability lost by most p53 mutants. We have previously reported that p53 mutant genes can rescue REF52 cells from ras-induced growth arrest and that over expression of wild type p53 inhibits cell growth in these cells. In this paper we examined whether p53 can also induce cell cycle arrest at the G2/M boundary of the cell cycle. To accomplish this we used the REF52 cell line and the temperature sensitive p53val135 mutant allele. Cells were enriched in the late G1 and early S phases before the temperature shift. REF52 cells expressing mutant-p53val135 alone with an activated H-ras gene arrest primarily at the G1/S and G2/M parts of the cell cycle at the restrictive temperature, as determined by flow cytometry analysis. These results suggest that the anti-proliferative activity of p53 may be involved in regulation of the cell cycle at the G2/M restriction point as well as transit through G1/S and initiation of DNA synthesis.

摘要

野生型p53可在细胞周期的特定点诱导细胞周期停滞,尤其是G1/S期,而大多数p53突变体则丧失了这种能力。我们之前报道过,p53突变基因可使REF52细胞从ras诱导的生长停滞中恢复,且野生型p53的过表达会抑制这些细胞的生长。在本文中,我们研究了p53是否也能在细胞周期的G2/M边界诱导细胞周期停滞。为实现这一目的,我们使用了REF52细胞系和温度敏感的p53val135突变等位基因。在温度转变前,细胞富集于G1晚期和S早期。通过流式细胞术分析确定,单独表达突变型p53val135并带有激活的H-ras基因的REF52细胞在限制温度下主要停滞在细胞周期的G1/S期和G2/M期。这些结果表明,p53的抗增殖活性可能参与了细胞周期在G2/M限制点的调控以及通过G1/S期和DNA合成起始的过程。

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