Medical Research Council, Toxicology Unit, Leicester University, Leicester, UK.
Cell Cycle. 2012 Dec 15;11(24):4545-51. doi: 10.4161/cc.22819. Epub 2012 Nov 19.
p63 is a transcriptional factor implicated in cancer and development. The presence in TP63 gene of alternative promoters allows expression of one isoform containing the N-terminal transactivation domain (TA isoform) and one N-terminal truncated isoform (ΔN isoform). Complete ablation of all p63 isoforms produced mice with fatal developmental abnormalities, including lack of epidermal barrier, limbs and other epidermal appendages. Specific TAp63-null mice, although they developed normally, failed to undergo in DNA damage-induced apoptosis during primordial follicle meiotic arrest, suggesting a p63 involvement in maternal reproduction. Recent findings have elucidated the role in DNA damage response of a novel Hominidae p63 isoform, GTAp63, specifically expressed in human spermatic precursors. Thus, these findings suggest a unique strategy of p63 gene, to evolve in order to preserve the species as a guardian of reproduction. Elucidation of the biological basis of p63 function in reproduction may provide novel approaches to the control of human fertility.
p63 是一种与癌症和发育有关的转录因子。TP63 基因中存在替代启动子,允许表达一种含有 N 端转录激活结构域(TA 结构域)的异构体和一种 N 端截断的异构体(ΔN 异构体)。完全消除所有 p63 异构体的小鼠会出现致命的发育异常,包括缺乏表皮屏障、四肢和其他表皮附属物。尽管特异性 TAp63 缺失的小鼠正常发育,但在原始卵泡减数分裂阻滞时未能发生 DNA 损伤诱导的细胞凋亡,表明 p63 参与了母体生殖。最近的研究结果阐明了新型 Hominidae p63 异构体 GTAp63 在 DNA 损伤反应中的作用,该异构体特异性表达于人类精子前体中。因此,这些发现表明 p63 基因存在一种独特的进化策略,以保护物种作为生殖的守护者。阐明 p63 在生殖中的生物学功能基础可能为控制人类生育能力提供新的方法。