Pringle Eric S, McCormick Craig, Cheng Zhenyu
Department of Microbiology and Immunology, Dalhousie University, Halifax, Nova Scotia, Canada.
Beatrice Hunter Cancer Research Institute, Halifax, Nova Scotia, Canada.
Curr Protoc Mol Biol. 2019 Jan;125(1):e79. doi: 10.1002/cpmb.79. Epub 2018 Oct 29.
Post-transcriptional regulation is an important aspect of the control of gene expression. mRNAs are translated with variable efficiencies, and these efficiencies can change rapidly during adaptation to diverse environmental factors, including cellular stresses and microbial infections. Polysome profiling analysis utilizes ultracentrifugation to isolate complexes of mRNAs in the process of translation and corresponding proteins on the basis of density. Here we describe polysome profiling analysis using a continuous ultraviolet spectrophotometer and a gradient fractionator. We provide protocols for processing sucrose gradient fractions for isolation of RNA for RT-qPCR analysis and isolation of protein for SDS-PAGE and immunoblot analysis. © 2018 by John Wiley & Sons, Inc.
转录后调控是基因表达控制的一个重要方面。信使核糖核酸(mRNA)的翻译效率各不相同,并且在适应各种环境因素(包括细胞应激和微生物感染)的过程中,这些效率会迅速变化。多核糖体谱分析利用超速离心,根据密度分离处于翻译过程中的mRNA复合物和相应的蛋白质。在此,我们描述了使用连续紫外分光光度计和梯度分级仪进行多核糖体谱分析的方法。我们提供了处理蔗糖梯度级分以分离用于逆转录定量聚合酶链反应(RT-qPCR)分析的RNA以及分离用于十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和免疫印迹分析的蛋白质的方案。© 2018约翰威立国际出版公司