p51A (TAp63γ), a p53 homolog, accumulates in response to DNA damage for cell regulation

被引:84
作者
Katoh, I
Aisaki, K
Kurata, S
Ikawa, S
Ikawa, Y [1 ]
机构
[1] Tokyo Med & Dent Univ, Div Med Res, Dept Retroviral Regulat, Tokyo 1138519, Japan
[2] Tokyo Med & Dent Univ, Human Gene Sci Ctr, Tokyo 1138510, Japan
[3] Tokyo Med & Dent Univ, Med Res Inst, Tokyo 1138510, Japan
[4] Tohoku Univ, Inst Dev Aging & Canc, Dept Cell Biol, Sendai, Miyagi 9808575, Japan
关键词
p51; p63; p53; p21(wafI); Bax; DNA damage;
D O I
10.1038/sj.onc.1203644
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
p51A, or TAp63 gamma, a translation product of gene p51, or p63, was identified as a homolog of p53 in its primary structure and transactivating function. p53 plays a decision-making role in inducing either cell cycle arrest or apoptosis in response to DNA damage, and thereby preserves genome integrity of living cells, To compare the biological activities between p51A and p53, cell lines with low-level, constitutive expression of each protein were obtained by cDNA transfection of mouse erythroleukemic cells. Production of p51A with an apparent molecular mass of 57-kilodalton (kD) accompanied induction of p21(wafl) and appearance of hemoglobin-producing cells. After DNA-damaging treatment either with ultraviolet light (UV) irradiation or with actinomycin D, the p51A protein accumulated in time courses corresponding to those of wild-type p53, and caused an increase in the hemoglobin-positive cell count. In contrast, p53-accumulated cells underwent apoptosis without exhibiting the feature of erythroid differentiation, The mode of p21(wafl) and Bax-alpha upregulations varied between p51A- and p53-expressing cells and between the types of DNA damage. These results suggest the possibility that p51A induces differentiation under genotoxic circumstances. There may be cellular factors that control p51A protein stability and transactivating ability.
引用
收藏
页码:3126 / 3130
页数:5
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