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猪体外卵母细胞成熟过程中MicroRNA-21和PDCD4的表达

MicroRNA-21 and PDCD4 expression during in vitro oocyte maturation in pigs.

作者信息

Wright Elane C, Hale Benjamin J, Yang Cai-Xia, Njoka Josephat G, Ross Jason W

机构信息

Department of Animal Science, Iowa State University, 2356 Kildee hall, Ames, IA, 50011, USA.

出版信息

Reprod Biol Endocrinol. 2016 Apr 16;14:21. doi: 10.1186/s12958-016-0152-2.

Abstract

BACKGROUND

MicroRNA (miRNA) are small non-coding RNA molecules critical for regulating cellular function, and are abundant in the maturing oocyte and developing embryo. MiRNA-21 (MIR21) has been shown to elicit posttranscriptional gene regulation in several tissues associated with rapid cell proliferation in addition to demonstrating anti-apoptotic features through interactions with PDCD4 mRNA and other targets. In many tissues, MIR21 interacts and suppresses PDCD4 due to the strong complementation between MIR21 and the PDCD4 3'UTR.

METHODS

The objective of this project was to examine the relationship between MIR21 and PDCD4 expression in porcine oocytes during in vitro maturation and assess the impact of MIR21 inhibition during oocyte maturation on early embryo development. Additionally, we evaluated the effect of gonadotropins in maturation media and the presence of cumulus cells to determine their ability to contribute to MIR21 abundance in the oocyte during maturation.

RESULTS

During in vitro maturation, expression of MIR21 increased approximately 6-fold in the oocyte and 25-fold in the cumulus cell. Temporally associated with this was the reduction of PDCD4 protein abundance in MII arrested oocytes compared with GV stage oocytes, although PDCD4 mRNA was not significantly different during this transition. Neither the presence of cumulus cells nor gonadotropins during in vitro maturation affected MIR21 abundance in those oocytes achieving MII arrest. However, inhibition of MIR21 activity during in vitro maturation using antisense MIR21 suppressed embryo development to the 4-8 cell stage following parthenogenetic activation.

CONCLUSIONS

MIR21 is differentially expressed in the oocyte during meiotic maturation in the pig and inhibition of MIR21 during this process alters PDCD4 protein abundance suggesting posttranscriptional regulatory events involving MIR21 during oocyte maturation may impact subsequent embryonic development in the pig.

摘要

背景

微小RNA(miRNA)是对调节细胞功能至关重要的小型非编码RNA分子,在成熟卵母细胞和发育中的胚胎中含量丰富。除了通过与PDCD4 mRNA和其他靶标相互作用表现出抗凋亡特性外,miRNA-21(MIR21)已被证明在与快速细胞增殖相关的几种组织中引发转录后基因调控。在许多组织中,由于MIR21与PDCD4 3'UTR之间的强互补性,MIR21与PDCD4相互作用并抑制PDCD4。

方法

本项目的目的是研究猪卵母细胞体外成熟过程中MIR21与PDCD4表达之间的关系,并评估卵母细胞成熟过程中MIR21抑制对早期胚胎发育的影响。此外,我们评估了促性腺激素在成熟培养基中的作用以及卵丘细胞的存在,以确定它们在成熟过程中对卵母细胞中MIR21丰度的影响能力。

结果

在体外成熟过程中,MIR21在卵母细胞中的表达增加了约6倍,在卵丘细胞中增加了25倍。与此时间相关的是,与GV期卵母细胞相比,MII期停滞卵母细胞中PDCD4蛋白丰度降低,尽管在此转变过程中PDCD4 mRNA没有显著差异。体外成熟过程中卵丘细胞的存在或促性腺激素的添加均未影响达到MII期停滞的卵母细胞中MIR21的丰度。然而,在体外成熟过程中使用反义MIR21抑制MIR21活性会抑制孤雌激活后胚胎发育至4-8细胞阶段。

结论

在猪减数分裂成熟过程中,MIR21在卵母细胞中差异表达,在此过程中抑制MIR21会改变PDCD4蛋白丰度,这表明卵母细胞成熟过程中涉及MIR21的转录后调控事件可能会影响猪随后的胚胎发育。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af9e/4833929/8da0f6940021/12958_2016_152_Fig1_HTML.jpg

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