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哺乳动物卵母细胞成熟过程中的细胞质多聚腺苷酸化

Cytoplasmic polyadenylation in mammalian oocyte maturation.

作者信息

Reyes Juan M, Ross Pablo J

机构信息

Department of Animal Science, University of California, Davis, CA, USA.

出版信息

Wiley Interdiscip Rev RNA. 2016 Jan-Feb;7(1):71-89. doi: 10.1002/wrna.1316. Epub 2015 Nov 24.

Abstract

Oocyte developmental competence is the ability of the mature oocyte to be fertilized and subsequently drive early embryo development. Developmental competence is acquired by completion of oocyte maturation, a process that includes nuclear (meiotic) and cytoplasmic (molecular) changes. Given that maturing oocytes are transcriptionally quiescent (as are early embryos), they depend on post-transcriptional regulation of stored transcripts for protein synthesis, which is largely mediated by translational repression and deadenylation of transcripts within the cytoplasm, followed by recruitment of specific transcripts in a spatiotemporal manner for translation during oocyte maturation and early development. Motifs within the 3' untranslated region (UTR) of messenger RNA (mRNA) are thought to mediate repression and downstream activation by their association with binding partners that form dynamic protein complexes that elicit differing effects on translation depending on cell stage and interacting proteins. The cytoplasmic polyadenylation (CP) element, Pumilio binding element, and hexanucleotide polyadenylation signal are among the best understood motifs involved in CP, and translational regulation of stored transcripts as their binding partners have been relatively well-characterized. Knowledge of CP in mammalian oocytes is discussed as well as novel approaches that can be used to enhance our understanding of the functional and contributing features to transcript CP and translational regulation during mammalian oocyte maturation. WIREs RNA 2016, 7:71-89. doi: 10.1002/wrna.1316 For further resources related to this article, please visit the WIREs website.

摘要

卵母细胞发育能力是指成熟卵母细胞受精并随后驱动早期胚胎发育的能力。发育能力是通过卵母细胞成熟来获得的,这一过程包括细胞核(减数分裂)和细胞质(分子)的变化。鉴于成熟中的卵母细胞转录静止(早期胚胎也是如此),它们依赖于对储存转录本进行转录后调控以进行蛋白质合成,这在很大程度上是由细胞质中转录本的翻译抑制和去腺苷酸化介导的,随后在卵母细胞成熟和早期发育过程中以时空方式募集特定转录本进行翻译。信使核糖核酸(mRNA)3'非翻译区(UTR)内的基序被认为通过与形成动态蛋白质复合物的结合伴侣相互作用来介导抑制和下游激活,这些蛋白质复合物根据细胞阶段和相互作用蛋白对翻译产生不同影响。细胞质聚腺苷酸化(CP)元件、Pumilio结合元件和六核苷酸聚腺苷酸化信号是参与CP以及储存转录本翻译调控的最被熟知的基序,因为它们的结合伴侣已得到较好的表征。本文讨论了哺乳动物卵母细胞中CP的相关知识,以及可用于增强我们对哺乳动物卵母细胞成熟过程中转录本CP和翻译调控的功能及贡献特征理解的新方法。WIREs RNA 2016, 7:71 - 89. doi: 10.1002/wrna.1316 有关本文的更多资源,请访问WIREs网站。

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