Haoudi Abdelali, Semmes O John, Mason James M, Cannon Ronald E
J Biomed Biotechnol. 2004;2004(4):185-194. doi: 10.1155/S1110724304403131.
Retrotransposition of human LINE-1 (L1) element, a major representative non-LTR retrotransposon in the human genome, is known to be a source of insertional mutagenesis. However, nothing is known about effects of L1 retrotransposition on cell growth and differentiation. To investigate the potential for such biological effects and the impact that human L1 retrotransposition has upon cancer cell growth, we examined a panel of human L1 transformed cell lines following a complete retrotransposition process. The results demonstrated that transposition of L1 leads to the activation of the p53-mediated apoptotic pathway in human cancer cells that possess a wild-type p53. In addition, we found that inactivation of p53 in cells, where L1 was undergoing retrotransposition, inhibited the induction of apoptosis. This suggests an association between active retrotransposition and a competent p53 response in which induction of apoptosis is a major outcome. These data are consistent with a model in which human retrotransposition is sensed by the cell as a "genetic damaging event" and that massive retrotransposition triggers signaling pathways resulting in apoptosis.
人类LINE-1(L1)元件是人类基因组中主要的非LTR逆转录转座子代表,其逆转录转座作用是插入诱变的一个来源。然而,关于L1逆转录转座对细胞生长和分化的影响却一无所知。为了研究这种生物学效应的可能性以及人类L1逆转录转座对癌细胞生长的影响,我们在完整的逆转录转座过程后检测了一组人类L1转化细胞系。结果表明,L1的转座导致了具有野生型p53的人类癌细胞中p53介导的凋亡途径的激活。此外,我们发现,在L1正在进行逆转录转座的细胞中p53失活会抑制凋亡的诱导。这表明活跃的逆转录转座与有效的p53反应之间存在关联,其中凋亡的诱导是主要结果。这些数据与一种模型一致,在该模型中,细胞将人类逆转录转座感知为一种“基因损伤事件”,大量的逆转录转座会触发信号通路导致凋亡。