Maier Bernhard, Gluba Wendy, Bernier Brian, Turner Terry, Mohammad Khalid, Guise Theresa, Sutherland Ann, Thorner Michael, Scrable Heidi
Department of Neuroscience, University of Virginia School of Medicine, Charlottesville, Virginia 22908, USA.
Genes Dev. 2004 Feb 1;18(3):306-19. doi: 10.1101/gad.1162404.
Overexpression of the short isoform of p53 (p44) has unexpectedly uncovered a role for p53 in the regulation of size and life span in the mouse. Hyperactivation of the insulin-like growth factor (IGF) signaling axis by p44 sets in motion a kinase cascade that clamps potentially unimpeded growth through p21Cip1. This suggests that pathways of gene activity known to regulate longevity in lower organisms are linked in mammals via p53 to mechanisms for controlling cell proliferation. Thus, appropriate expression of the short and long p53 isoforms might maintain a balance between tumor suppression and tissue regeneration, a major requisite for long mammalian life span.
p53短异构体(p44)的过表达意外地揭示了p53在调节小鼠体型和寿命方面的作用。p44对胰岛素样生长因子(IGF)信号轴的过度激活启动了一个激酶级联反应,该反应通过p21Cip1抑制可能不受阻碍的生长。这表明,在低等生物中已知调节寿命的基因活性途径在哺乳动物中通过p53与控制细胞增殖的机制相联系。因此,p53短异构体和长异构体的适当表达可能维持肿瘤抑制和组织再生之间的平衡,这是哺乳动物长寿的一个主要必要条件。