辐射诱导的细胞循环停止受到p21缺乏症的危害
J Brugarolas1, C Chandrasekaran, J I Gordon
1Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge 02139, USA.
Nature
|October 12, 1995
概括
细胞循环抑制剂的蛋白质p21不会影响肠道细胞分化或DNA损伤诱导的亡. 然而,p21缺乏会影响DNA损伤后小鼠纤维细胞的G1细胞周期停止.
科学领域:
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
- 遗传学 是一个遗传学.
背景情况:
- 蛋白质p21作为循环素依赖激酶和增殖细胞核抗原 (PCNA) 的双重抑制剂,对细胞循环进展至关重要.
- p21基因受到p53的调节,这表明它在p53依赖的细胞循环停止和细胞亡中的作用.
- p21还与终端分化期间的细胞衰老和细胞周期退出有关.
研究的目的:
- 研究p21在细胞循环调节,分化和亡中的作用.
- 用转基因小鼠模型确定p21的体内功能.
主要方法:
- 使用了由p21淘汰赛 (p21-/-) 和野生类型 (p21+/+) 细胞组成的基马体小鼠.
- 对成年小肠部件进行了免疫组织化学分析.
- 在p21-/-小鼠胚胎纤维细胞中经过DNA损伤后评估的G1停滞.
主要成果:
- 删除p21对肠上皮细胞的分化没有明显的影响.
- 在对照射的反应中,p21缺乏没有影响p53依赖的亡.
- p21-/-小鼠胚胎纤维细胞在DNA损伤后表现出G1停止受损.
结论:
- 对于肠道上皮细胞分化或辐射诱导的亡,p21不是必不可少的.
- p21在促进G1细胞循环停止,以应对DNA损伤方面发挥着至关重要的作用.
- 这些发现澄清了p21在细胞循环控制和组织平衡中的特定功能.
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