Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, United Kingdom.
PLoS One. 2010 Jan 13;5(1):e8369. doi: 10.1371/journal.pone.0008369.
p300 functions as a transcriptional co-activator to regulate many cellular responses such as cell growth, transformation, development and differentiation. It has been shown to affect the transcriptional activity of p53 which regulates p21(Waf1/CIP1) expression, however, the role of p300 in differentiation remains unclear.
Knockdown of p300 protein with short hairpin RNA (shRNA) molecules delays human neonatal foreskin keratinocyte (HFKs) differentiation. Moreover, depletion of p300 increases the proliferative capacity of HFKs, extends the life span of cells and allows differentiated HFKs to re-enter the cell cycle. Studies indicate that depletion of p300 down-regulates the acetylation and expression of p53, and chromatin immunoprecipitation (ChIP) analysis shows that induction of p21(Waf1/CIP1) in early differentiation is a result of p300 dependent activation of p53 and that depletion of p21(Waf1/CIP1) results in the delay of differentiation and a phenotype similar to p300 depletion.
p300 has a direct role in the control of cell growth and differentiation in primary epithelial cells, and p21(Waf1/CIP1) is an important mediator of these p300 functions.
p300 作为转录共激活因子,调节细胞生长、转化、发育和分化等多种细胞反应。已证实其影响调节 p21(Waf1/CIP1) 表达的 p53 的转录活性,但 p300 在分化中的作用尚不清楚。
短发夹 RNA (shRNA) 分子敲低 p300 蛋白可延迟人新生儿包皮角质细胞 (HFKs) 的分化。此外,p300 的耗竭增加了 HFKs 的增殖能力,延长了细胞寿命,并使分化的 HFKs 重新进入细胞周期。研究表明,p300 的耗竭下调了 p53 的乙酰化和表达,染色质免疫沉淀 (ChIP) 分析表明,早期分化中 p21(Waf1/CIP1) 的诱导是 p300 依赖性 p53 激活的结果,p21(Waf1/CIP1) 的耗竭导致分化延迟,并表现出类似于 p300 耗竭的表型。
p300 在原代上皮细胞的细胞生长和分化控制中具有直接作用,p21(Waf1/CIP1) 是这些 p300 功能的重要介质。