期刊
ONCOGENE
卷 22, 期 48, 页码 7607-7616出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/sj.onc.1207129
关键词
p53; p63; mammary epithelia; gene regulation
Mammary epithelial regeneration implies the existence of cellular progenitors with retained replicative capacity, prolonged lifespan and developmental potency. Evidence exists that DeltaN-p63 isoforms preserve these features by modulating p53 activity in basal epithelia. DeltaN-p63 mRNA levels decline at the onset of differentiation suggesting that its transcriptional regulation may contribute to the initiation of differentiation. To study transcriptional regulation of DeltaN-p63, a 10.3 kbp fragment containing the DeltaN-p63 promoter was isolated. We report here that DeltaN-p63 is a positive and negative transcriptional target of p53 and DeltaN-p63-alpha, respectively. Disruption of p53 activity or expression abolishes the expression of DeltaN-p63-alpha. This regulation is mediated by a p53-binding element sufficient to confer these activities to a heterologous promoter. Chromatin immune-precipitation indicates that, in asynchronously growing cells, p53 occupies this element. In response to DNA damage, DeltaN-p63-alpha is recruited to this element as transcription of DeltaN-p63 declines. Disruption of DeltaN-p63-alpha expression had differential effects on the transcriptional regulation of several p53-target genes. These findings indicate that p53 contributes to the preservation of basal epithelia by driving the expression of DeltaN-p63 isoforms. These studies also suggest that in response to genotoxic stress, DeltaN-p63-alpha mediates the silencing of its own promoter thereby altering the pattern of p53-target gene expression.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据