Regulation of maternal mRNA translation during early development

早期发育过程中母体 mRNA 翻译的调节

• 批准号: 8599714
• 负责人: EMRE UTKU SELI
• 金额: $ 34.39万
• 依托单位: YALE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-12-21 至 2015-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8599714
• 关键词: Affect; Age; Aging; Binding; Clinical; Collection; Complex; Development; Disease; Embryo; Embryo Loss; Embryonic Development; Female; Female infertility; Fertility; Fertilization; Gene Expression; Gene Expression Regulation; Genetic Transcription; Genetic Translation; Genome; Goals; Human; Human Development; Infertility; Knockout Mice; Maternal Messenger RNA; Mediating; Meiosis; Messenger RNA; Microinjections; Molecular; Mus; Nuclear; Oocytes; Oogenesis; Ovulation; Pathway interactions; Phenotype; Phosphorylation; Phosphotransferases; Play; Poly(A)-Binding Proteins; Polyadenylation; Preparation; Prophase; Protein Isoforms; Proteins; RNA, Messenger, Stored; Regulation; Regulator Genes; Research; Role; Staging; Stimulus; Testing; Time; Translating; Translational Activation; Translations; Vesicle; Woman; Xenopus; Xenopus oocyte; critical period; egg; improved; meetings; mouse model; oocyte maturation; ovulation disorders; protein complex; public health relevance; reproductive; therapeutic target

DESCRIPTION (provided by applicant): The overall aim of this proposal is to better understand the regulation of gene expression during mammalian oocyte and early embryo development. Oocyte maturation is associated with suppression of transcription. Consequently, gene expression during oocyte maturation, fertilization, and early embryo development until zygotic genome activation (ZGA), is regulated by translational activation of maternally- stored mRNAs. Embryonic poly(A) binding protein (ePAB) is the predominant poly(A) binding protein during Xenopus, mouse and human oocyte and early embryo development until ZGA. In Xenopus, ePAB is required for both known pathways (cytoplasmic polyadenylation-dependent and independent) that mediate maternal mRNA translational activation upon oocyte maturation. In addition, our preliminary findings demonstrate that oocyte maturation is inhibited when ePAB activity is suppressed in Xenopus oocytes, and that ePAB-deficient female mice are infertile due to impaired oogenesis. We therefore hypothesize that ePAB plays a key role in the regulation of gene expression during a critical period of early development, when transcription is suppressed. Here, we propose to characterize the cellular and molecular aspects of infertility in ePAB-deficient mice and to determine regulation of ePAB's function by phosphorylation. The specific aims of this proposal are to: 1. Determine ePAB-null phenotype using a knockout mouse model. 2. Determine the role of ePAB phosphorylation in the regulation of maternal mRNA translational activation and oocyte maturation. These proposed studies focus on early development, and consequently the results obtained will have ramifications for human development and fertility.

描述（由申请人提供）：本提案的总体目标是更好地了解哺乳动物卵母细胞和早期胚胎发育过程中基因表达的调控。卵母细胞成熟与转录抑制有关。因此，卵母细胞成熟、受精和早期胚胎发育直至合子基因组激活（ZGA）期间的基因表达受母体储存的mRNA的翻译激活调节。胚胎多聚腺苷酸结合蛋白（ePAB）是非洲爪蟾、小鼠和人类卵母细胞以及早期胚胎发育直至ZGA期间的主要多聚腺苷酸结合蛋白。在非洲爪蟾中，ePAB是卵母细胞成熟时介导母体mRNA翻译激活的两种已知途径（细胞质多聚腺苷酸化依赖性和非依赖性）所必需的。此外，我们的初步研究结果表明，卵母细胞的成熟受到抑制时，抑制非洲爪蟾卵母细胞的ePAB活性，和ePAB缺陷的雌性小鼠是不育的，由于受损的卵子发生。因此，我们假设ePAB在转录被抑制的早期发育的关键时期在基因表达的调节中起关键作用。在这里，我们建议ePAB缺陷小鼠不育的细胞和分子方面的特点，并确定ePAB的磷酸化功能的调节。这项建议的具体目标是：1.使用敲除小鼠模型确定ePAB无效表型。2.确定ePAB磷酸化在调节母体mRNA翻译激活和卵母细胞成熟中的作用。这些拟议的研究重点是早期发育，因此所获得的结果将对人类发育和生育产生影响。