International Institute of Molecular and Cell Biology in Warsaw, Warsaw, Poland.
Max Planck Institute for Heart and Lung Research, Bad-Nauheim, Germany.
Methods Mol Biol. 2021;2218:367-380. doi: 10.1007/978-1-0716-0970-5_29.
The study of translational regulation requires reliable measurement of both mRNA levels and protein synthesis. Cytoplasmic polyadenylation is a prevalent mode of translational regulation during oogenesis and early embryogenesis. Here the length of the poly(A) tail of an mRNA is coupled to its translatability. We describe a protocol to identify translationally regulated genes and measure their translation rate in the early zebrafish embryo using genome-wide polysome profiling. This protocol relies on the isolation of mRNA by means of an rRNA depletion strategy, which avoids capture bias due to short poly(A) tail that can occur when using conventional oligo(dT)-based methods. We also present a simple PCR-based method to measure the poly(A) tail length of selected mRNAs.
将这段英文翻译成中文,不要添加任何解释或说明。
该研究需要可靠的翻译调节mRNA 水平和蛋白质合成的测量。细胞质多聚腺苷酸化是一种普遍的调节方式在卵子发生和早期胚胎发生过程中的翻译。在这里,mRNA 的 poly(A)尾巴的长度与其可翻译性相关联。我们描述了一种使用全基因组多核糖体分析来鉴定翻译调节基因并测量其在早期斑马鱼胚胎中的翻译速率的方案。该方案依赖于通过 rRNA 耗尽策略来分离 mRNA,这可以避免由于使用常规寡聚(dT)-基于方法而导致的短 poly(A)尾巴引起的捕获偏差。我们还提出了一种简单的基于 PCR 的方法来测量选定 mRNA 的 poly(A)尾巴长度。