Xu Wenting, Mo Yanxiu, He Yu, Fan Yunpeng, He Guomin, Fu Wen, Chen Shujuan, Liu Jinhui, Liu Wenbin, Peng Liangyue, Xiao Yamei
State Key Laboratory of Developmental Biology of Freshwater Fish, Hunan Normal University, Changsha, China.
College of Life Sciences, Hunan Normal University, Changsha, China.
Front Bioeng Biotechnol. 2021 Jan 13;8:606496. doi: 10.3389/fbioe.2020.606496. eCollection 2020.
Previous studies have suggested that 1,9-Pyrazoloanthrone, known as SP600125, can induce cell polyploidization. However, what is the phase of cell cycle arrest caused by SP600125 and the underlying regulation is still an interesting issue to be further addressed. Research in this article shows that SP600125 can block cell cycle progression at the prometaphase of mitosis and cause endomitosis. It is suggested that enhancement of the p53 signaling pathway and weakening of the spindle assembly checkpoint are associated with the SP600125-induced cell cycle arrest. Using preliminary SP600125 treatment, the samples of the cultured fish cells and the fish tissues display a great number of chromosome splitting phases. Summarily, SP600125 can provide a new protocol of chromosomes preparation for karyotype analysis owing to its interference with prometaphase of mitosis.
先前的研究表明,1,9-吡唑并蒽酮(即SP600125)可诱导细胞多倍体化。然而,SP600125导致细胞周期阻滞的阶段以及潜在的调控机制仍是一个有待进一步探讨的有趣问题。本文的研究表明,SP600125可在有丝分裂的前中期阻断细胞周期进程并导致核内有丝分裂。提示p53信号通路增强和纺锤体组装检查点减弱与SP600125诱导的细胞周期阻滞有关。使用初步的SP600125处理后,培养的鱼类细胞和鱼类组织样本显示出大量的染色体分裂期。总之,SP600125因其对有丝分裂前中期的干扰可为核型分析提供一种新的染色体制备方案。