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首页> 外文期刊>BMC Molecular Biology >Characterization of the transcripts and protein isoforms for cytoplasmic polyadenylation element binding protein-3 (CPEB3) in the mouse retina
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Characterization of the transcripts and protein isoforms for cytoplasmic polyadenylation element binding protein-3 (CPEB3) in the mouse retina

机译:小鼠视网膜中胞质聚腺苷酸化元素结合蛋白3(CPEB3)的转录本和蛋白同工型的表征

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Background Cytoplasmic polyadenylation element binding proteins (CPEBs) regulate translation by binding to regulatory motifs of defined mRNA targets. This translational mechanism has been shown to play a critical role in oocyte maturation, early development, and memory formation in the hippocampus. Little is known about the presence or functions of CPEBs in the retina. The purpose of the current study is to investigate the alternative splicing isoforms of a particular CPEB, CPEB3, based on current databases, and to characterize the expression of CPEB3 in the retina. Results In this study, we have characterized CPEB3, whose putative role is to regulate the translation of GluR2 mRNA. We identify the presence of multiple alternative splicing isoforms of CPEB3 transcripts and proteins in the current databases. We report the presence of eight alternative splicing patterns of CPEB3, including a novel one, in the mouse retina. All but one of the patterns appear to be ubiquitous in 13 types of tissue examined. The relative abundance of the patterns in the retina is demonstrated. Experimentally, we show that CPEB3 expression is increased in a time-dependent manner during the course of postnatal development, and CPEB3 is localized mostly in the inner retina, including retinal ganglion cells. Conclusion The level of CPEB3 was up-regulated in the retina during development. The presence of multiple CPEB3 isoforms indicates remarkable complexity in the regulation and function of CPEB3.
机译:背景细胞质聚腺苷酸化元件结合蛋白(CPEB)通过与定义的mRNA靶标的调控基序结合来调控翻译。已经证明这种翻译机制在海马的卵母细胞成熟,早期发育和记忆形成中起关键作用。关于CPEB在视网膜中的存在或功能知之甚少。本研究的目的是基于当前数据库研究特定CPEB CPEB3的可变剪接同工型,并表征CPEB3在视网膜中的表达。结果在这项研究中,我们表征了CPEB3,其可能的作用是调节GluR2 mRNA的翻译。我们确定在当前数据库中CPEB3成绩单和蛋白质的多个替代剪接异构体的存在。我们报告CPEB3的八个替代剪接模式的存在,包括一个新颖的,在小鼠视网膜中。除了一种模式外,所有模式均在检查的13种组织中普遍存在。视网膜中图案的相对丰度得到了证明。实验上,我们显示CPEB3的表达在出生后的发展过程中以时间依赖的方式增加,并且CPEB3大部分位于视网膜内,包括视网膜神经节细胞。结论在发育过程中视网膜中CPEB3的水平上调。多种CPEB3亚型的存在表明CPEB3的调控和功能异常复杂。

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