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Ral GTP酶对小鼠卵母细胞成熟过程中的肌动蛋白动力学和高尔基体分布至关重要。

Ral GTPase is essential for actin dynamics and Golgi apparatus distribution in mouse oocyte maturation.

作者信息

Sun Ming-Hong, Hu Lin-Lin, Zhao Chao-Ying, Lu Xiang, Ren Yan-Ping, Wang Jun-Li, Cui Xiang-Shun, Sun Shao-Chen

机构信息

Department of Animal Sciences, Chungbuk National University, Cheongju, 28644, South Korea.

College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, China.

出版信息

Cell Div. 2021 Jun 10;16(1):3. doi: 10.1186/s13008-021-00071-y.

DOI:10.1186/s13008-021-00071-y
PMID:34112192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8194175/
Abstract

BACKGROUND

Ral family is a member of Ras-like GTPase superfamily, which includes RalA and RalB. RalA/B play important roles in many cell biological functions, including cytoskeleton dynamics, cell division, membrane transport, gene expression and signal transduction. However, whether RalA/B involve into the mammalian oocyte meiosis is still unclear. This study aimed to explore the roles of RalA/B during mouse oocyte maturation.

RESULTS

Our results showed that RalA/B expressed at all stages of oocyte maturation, and they were enriched at the spindle periphery area after meiosis resumption. The injection of RalA/B siRNAs into the oocytes significantly disturbed the polar body extrusion, indicating the essential roles of RalA/B for oocyte maturation. We observed that in the RalA/B knockdown oocytes the actin filament fluorescence intensity was significantly increased at the both cortex and cytoplasm, and the chromosomes were failed to locate near the cortex, indicating that RalA/B regulate actin dynamics for spindle migration in mouse oocytes. Moreover, we also found that the Golgi apparatus distribution at the spindle periphery was disturbed after RalA/B depletion.

CONCLUSIONS

In summary, our results indicated that RalA/B affect actin dynamics for chromosome positioning and Golgi apparatus distribution in mouse oocytes.

摘要

背景

Ral家族是Ras样GTP酶超家族的成员,包括RalA和RalB。RalA/B在许多细胞生物学功能中发挥重要作用,包括细胞骨架动力学、细胞分裂、膜运输、基因表达和信号转导。然而,RalA/B是否参与哺乳动物卵母细胞减数分裂仍不清楚。本研究旨在探讨RalA/B在小鼠卵母细胞成熟过程中的作用。

结果

我们的结果表明,RalA/B在卵母细胞成熟的各个阶段均有表达,减数分裂恢复后它们富集于纺锤体周边区域。向卵母细胞中注射RalA/B的小干扰RNA(siRNAs)显著干扰了极体排出,表明RalA/B对卵母细胞成熟至关重要。我们观察到,在敲低RalA/B的卵母细胞中,皮质和细胞质中的肌动蛋白丝荧光强度均显著增加,并且染色体未能定位在皮质附近,这表明RalA/B调节肌动蛋白动力学以促进小鼠卵母细胞中的纺锤体迁移。此外,我们还发现RalA/B缺失后纺锤体周边的高尔基体分布受到干扰。

结论

总之,我们的结果表明,RalA/B影响小鼠卵母细胞中染色体定位和高尔基体分布的肌动蛋白动力学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/8194175/4eaa650a2863/13008_2021_71_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/8194175/ae13e40d5a74/13008_2021_71_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/8194175/255cdaa54a57/13008_2021_71_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/8194175/f995c2522ab9/13008_2021_71_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/8194175/1df4c7f85adc/13008_2021_71_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/8194175/4eaa650a2863/13008_2021_71_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/8194175/ae13e40d5a74/13008_2021_71_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/8194175/255cdaa54a57/13008_2021_71_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/8194175/f995c2522ab9/13008_2021_71_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/8194175/1df4c7f85adc/13008_2021_71_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d24/8194175/4eaa650a2863/13008_2021_71_Fig5_HTML.jpg

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