Departmento de Biología Molecular, Instituto de Investigaciones Químico-Biológicas, Universidad Michoacana de San Nicolás de Hidalgo, Morelia, Michoacán, México.
Cell Div. 2010 May 13;5:10. doi: 10.1186/1747-1028-5-10.
Transcriptional and postranslational regulation of the cell cycle has been widely studied. However, there is scarce knowledge concerning translational control of this process. Several mammalian eukaryotic initiation factors (eIFs) seem to be implicated in controlling cell proliferation. In this work, we investigated if the human eIF3f expression and function is cell cycle related.
The human eIF3f expression has been found to be upregulated in growth-stimulated A549 cells and downregulated in G0. Western blot analysis and eIF3f promotor-luciferase fusions revealed that eIF3f expression peaks twice in the cell cycle: in the S and the M phases. Deregulation of eIF3f expression negatively affects cell viability and induces apoptosis.
The expression pattern of human eIF3f during the cell cycle confirms that this gene is cell division related. The fact that eIF3f expression peaks in two cell cycle phases raises the possibility that this gene may exert a differential function in the S and M phases. Our results strongly suggest that eIF3f is essential for cell proliferation.
细胞周期的转录和翻译后调控已经得到了广泛的研究。然而,对于这个过程的翻译控制知之甚少。几种哺乳动物真核起始因子(eIFs)似乎参与了细胞增殖的控制。在这项工作中,我们研究了人类 eIF3f 的表达和功能是否与细胞周期有关。
发现人类 eIF3f 的表达在生长刺激的 A549 细胞中上调,在 G0 期下调。Western blot 分析和 eIF3f 启动子-荧光素酶融合显示,eIF3f 的表达在细胞周期中两次达到峰值:在 S 期和 M 期。eIF3f 表达的失调会降低细胞活力并诱导细胞凋亡。
eIF3f 在细胞周期中的表达模式证实了该基因与细胞分裂有关。eIF3f 在两个细胞周期阶段达到峰值的事实表明,该基因在 S 期和 M 期可能发挥不同的功能。我们的结果强烈表明 eIF3f 对于细胞增殖是必不可少的。