Department of Biochemistry and Molecular Biology; Cumming School of Medicine, University of Calgary; Alberta Children's Hospital Research Institute, University of Calgary.
Department of Medical Genetics, Cumming School of Medicine, University of Calgary; Alberta Children's Hospital Research Institute, University of Calgary.
J Vis Exp. 2021 May 22(171). doi: 10.3791/62088.
The proper development of the mammalian brain relies on a fine balance of neural stem cell proliferation and differentiation into different neural cell types. This balance is tightly controlled by gene expression that is fine-tuned at multiple levels, including transcription, post-transcription and translation. In this regard, a growing body of evidence highlights a critical role of translational regulation in coordinating neural stem cell fate decisions. Polysome fractionation is a powerful tool for the assessment of mRNA translational status at both global and individual gene levels. Here, we present an in-house polysome profiling pipeline to assess translational efficiency in cells from the developing mouse cerebral cortex. We describe the protocols for sucrose gradient preparation, tissue lysis, ultracentrifugation and fractionation-based analysis of mRNA translational status.
哺乳动物大脑的正常发育依赖于神经干细胞增殖和分化为不同神经细胞类型之间的精细平衡。这种平衡受到基因表达的严格控制,而基因表达在多个层面上进行微调,包括转录、转录后和翻译。在这方面,越来越多的证据强调了翻译调控在协调神经干细胞命运决定中的关键作用。多核糖体分段是评估全局和个体基因水平 mRNA 翻译状态的有力工具。在这里,我们提供了一个内部的多核糖体分析工作流程,用于评估来自发育中的小鼠大脑皮层细胞的翻译效率。我们描述了蔗糖梯度制备、组织裂解、超速离心和基于分馏的 mRNA 翻译状态分析的方案。