Aramayo Rodolfo, Polymenis Michael
Department of Biology, Texas A&M University, College Station, TX, 77845, USA.
Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX, 77845, USA.
Curr Genet. 2017 Dec;63(6):959-964. doi: 10.1007/s00294-017-0698-3. Epub 2017 Apr 27.
Understanding the causes and consequences of dynamic changes in the abundance and activity of cellular components during cell division is what most cell cycle studies are about. Here we focus on control of gene expression in the cell cycle at the level of translation. The advent of deep sequencing methodologies led to technologies that quantify the levels of all mRNAs that are bound by ribosomes and engaged in translation in the cell (Ingolia et al. Science 324:218-223, 2009). This approach has been applied recently to synchronous cell populations to find transcripts under translational control at different cell cycle phases (Blank et al. EMBO J 36:487-502, 2017; Stumpf et al. Mol Cell 52:574-582, 2013; Tanenbaum et al. Elife 4:e07957, 2015). These studies revealed new biology, but they also have limitations, pointing to challenges that need to be addressed in the future.
了解细胞分裂过程中细胞成分丰度和活性动态变化的原因及后果是大多数细胞周期研究的内容。在此,我们聚焦于细胞周期中翻译水平的基因表达调控。深度测序方法的出现催生了一些技术,这些技术能够对细胞中与核糖体结合并参与翻译的所有mRNA的水平进行定量(英戈利亚等人,《科学》324:218 - 223,2009年)。最近,这种方法已应用于同步化的细胞群体,以寻找在不同细胞周期阶段处于翻译调控下的转录本(布兰克等人,《欧洲分子生物学组织杂志》36:487 - 502,2017年;施通普夫等人,《分子细胞》52:574 - 582,2013年;塔嫩鲍姆等人,《eLife》4:e07957,2015年)。这些研究揭示了新的生物学现象,但也存在局限性,指出了未来需要解决的挑战。