Chassé Héloïse, Boulben Sandrine, Glippa Virginie, Pontheaux Florian, Cormier Patrick, Morales Julia
CNRS, Sorbonne Université, Integrative Biology of Marine Models (LBI2M), Station Biologique de Roscoff (SBR), Roscoff, France.
CNRS, Sorbonne Université, Integrative Biology of Marine Models (LBI2M), Station Biologique de Roscoff (SBR), Roscoff, France.
Methods Cell Biol. 2019;151:335-352. doi: 10.1016/bs.mcb.2018.10.008. Epub 2018 Dec 13.
Protein synthesis is a major regulatory step of gene expression in different physiological processes including development. Translation of proteins in sea urchin is stimulated upon fertilization and is necessary for cell cycle progression and development. Translational control is exerted through multifactorial mechanisms, including mRNA recruitment into polysomes and increased rates of translational activity. In this chapter, we review the methods used in sea urchin eggs and embryos to analyze translation activity in vivo both from perspectives of the proteins and of the mRNAs. First, we describe methods to quantify or visualize newly synthesized proteins with radioactive and non-radioactive labeling techniques. Next we present the polysome isolation and profiling on sucrose gradients, allowing the identification of translated mRNAs. Finally, we outline a procedure to follow the translation of a reporter luciferase protein from an mRNA microinjected into the egg.
蛋白质合成是包括发育在内的不同生理过程中基因表达的主要调控步骤。海胆受精后蛋白质翻译受到刺激,这对细胞周期进程和发育是必需的。翻译控制通过多因素机制发挥作用,包括mRNA募集到多核糖体中以及翻译活性速率的增加。在本章中,我们从蛋白质和mRNA两个角度综述了用于海胆卵和胚胎中分析体内翻译活性的方法。首先,我们描述了用放射性和非放射性标记技术定量或可视化新合成蛋白质的方法。接下来,我们介绍了蔗糖梯度上的多核糖体分离和分析,从而能够鉴定已翻译的mRNA。最后,我们概述了一种追踪从显微注射到卵中的mRNA翻译报告荧光素酶蛋白的程序。