Coudert Laëtitia, Adjibade Pauline, Mazroui Rachid
Department of Molecular Biology, Medical Biochemistry, and Pathology, Faculty of Medicine, Laval University; CHU de Quebec Research Center.
Department of Molecular Biology, Medical Biochemistry, and Pathology, Faculty of Medicine, Laval University; CHU de Quebec Research Center;
J Vis Exp. 2014 May 19(87):51164. doi: 10.3791/51164.
Precise control of mRNA translation is fundamental for eukaryotic cell homeostasis, particularly in response to physiological and pathological stress. Alterations of this program can lead to the growth of damaged cells, a hallmark of cancer development, or to premature cell death such as seen in neurodegenerative diseases. Much of what is known concerning the molecular basis for translational control has been obtained from polysome analysis using a density gradient fractionation system. This technique relies on ultracentrifugation of cytoplasmic extracts on a linear sucrose gradient. Once the spin is completed, the system allows fractionation and quantification of centrifuged zones corresponding to different translating ribosomes populations, thus resulting in a polysome profile. Changes in the polysome profile are indicative of changes or defects in translation initiation that occur in response to various types of stress. This technique also allows to assess the role of specific proteins on translation initiation, and to measure translational activity of specific mRNAs. Here we describe our protocol to perform polysome profiles in order to assess translation initiation of eukaryotic cells and tissues under either normal or stress growth conditions.
精确控制mRNA翻译对于真核细胞的稳态至关重要,尤其是在应对生理和病理应激时。这一程序的改变会导致受损细胞的生长,这是癌症发展的一个标志,或者导致过早的细胞死亡,如在神经退行性疾病中所见。关于翻译控制分子基础的许多已知信息是通过使用密度梯度分级系统的多核糖体分析获得的。该技术依赖于在线性蔗糖梯度上对细胞质提取物进行超速离心。一旦离心完成,该系统允许对对应于不同翻译核糖体群体的离心区进行分级和定量,从而得到多核糖体图谱。多核糖体图谱的变化表明了响应各种类型应激时翻译起始的变化或缺陷。该技术还允许评估特定蛋白质在翻译起始中的作用,并测量特定mRNA的翻译活性。在这里,我们描述了我们进行多核糖体图谱分析的方案,以评估正常或应激生长条件下真核细胞和组织的翻译起始情况。