Center for Reproductive Sciences, University of California at San Francisco; Department of Obstetrics Gynecology and Reproductive Sciences, University of California at San Francisco.
Center for Reproductive Sciences, University of California at San Francisco; Department of Obstetrics Gynecology and Reproductive Sciences, University of California at San Francisco; Present affiliation: Laboratoire de Biologie du Développement-Institut de Biologie Paris Seine, LBD-IBPS, Sorbonne Université.
J Vis Exp. 2021 Jun 16(172). doi: 10.3791/62041.
Events associated with oocyte nuclear maturation have been well described. However, much less is known about the molecular pathways and processes that take place in the cytoplasm in preparation for fertilization and acquisition of totipotency. During oocyte maturation, changes in gene expression depend exclusively on the translation and degradation of maternal messenger RNAs (mRNAs) rather than on transcription. Execution of the translational program, therefore, plays a key role in establishing oocyte developmental competence to sustain embryo development. This paper is part of a focus on defining the program of maternal mRNA translation that takes place during meiotic maturation and at the oocyte-to-zygote transition. In this method paper, a strategy is presented to study the regulation of translation of target mRNAs during in vitro oocyte maturation. Here, a Ypet reporter is fused to the 3' untranslated region (UTR) of the gene of interest and then micro-injected into oocytes together with polyadenylated mRNA encoding for mCherry to control for injected volume. By using time-lapse microscopy to measure reporter accumulation, translation rates are calculated at different transitions during oocyte meiotic maturation. Here, the protocols for oocyte isolation and injection, time-lapse recording, and data analysis have been described, using the Ypet/interleukin-7 (IL-7)-3' UTR reporter as an example.
卵母细胞核成熟相关事件已得到充分描述。然而,对于细胞质中为受精和获得全能性所进行的分子途径和过程,人们知之甚少。在卵母细胞成熟过程中,基因表达的变化完全依赖于母体信使 RNA(mRNA)的翻译和降解,而不是转录。因此,执行翻译程序对于建立卵母细胞发育能力以维持胚胎发育至关重要。本文是聚焦于定义母本 mRNA 翻译程序的一部分,该程序发生在减数分裂成熟和卵母细胞到受精卵的过渡期间。在本文的方法部分,提出了一种在体外卵母细胞成熟过程中研究目标 mRNA 翻译调控的策略。在这里,将 Ypet 报告基因融合到感兴趣基因的 3'非翻译区(UTR),然后与聚腺苷酸化的编码 mCherry 的 mRNA 一起微注射到卵母细胞中,以控制注射体积。通过使用延时显微镜测量报告基因的积累,可以在卵母细胞减数分裂成熟的不同阶段计算翻译速率。本文以 Ypet/白细胞介素 7(IL-7)-3'UTR 报告基因为例,描述了卵母细胞分离和注射、延时记录和数据分析的方案。