Suppr超能文献

纺锤体相关蛋白1对猪卵母细胞减数第二次分裂中期的维持及染色体稳定性至关重要。

Spindlin 1 is essential for metaphase II stage maintenance and chromosomal stability in porcine oocytes.

作者信息

Choi Jeong-Woo, Zhao Ming-Hui, Liang Shuang, Guo Jing, Lin Zi-Li, Li Ying-Hua, Jo Yu-Jin, Kim Nam-Hyung, Cui Xiang-Shun

机构信息

Department of Animal Science, Chungbuk National University, Cheongju, Chungbuk 361-763, Republic of Korea.

Division of Animal Biotechnology, National Institute of Animal Science, Rural Development Administration, Jeonju 55536, Republic of Korea.

出版信息

Mol Hum Reprod. 2017 Mar 1;23(3):166-176. doi: 10.1093/molehr/gax005.

Abstract

STUDY QUESTION

What is the function of Spindlin 1 (Spin1) in metaphase II stage oocytes in pigs?

SUMMARY ANSWER

Depletion of Spin1 induces spontaneous oocyte activation and overexpression of Spin1 causes multinuclear formation through induction of DNA damage in porcine oocytes.

WHAT IS KNOWN ALREADY

Little is known about the function of Spin1 in oocytes and embryos. In mouse oocytes, Spin1 is specifically expressed during gametogenesis and is essential for meiotic resumption. In somatic cells, Spin1 promotes cancer cell proliferation and activates WNT/T-cell factor signaling.

STUDY DESIGN SIZE, DURATION: After knockdown (KD) or overexpression of Spin1 in porcine MII-stage oocytes, MII maintenance was checked following additional culture for 24 h. Investigated parthenotes were cultured up to the four cell (72 h) or blastocyst (7 days) stages.

PARTICIPANTS/MATERIALS, SETTING, METHODS: Spin1 was knocked down in porcine oocytes and embryos via microinjection of pig Spin1-targeting siRNA. For Spin1 overexpression, porcine Spin1-eGFP cRNA was generated. Additionally, for rescue experiments, cRNA encoding siRNA-resistant mouse Spin1 was added to the pig Spin1-targeting siRNA. For the overexpression and rescue experiments, microinjection and culture were performed using the same methods as the KD experiments.

MAIN RESULTS AND THE ROLE OF CHANCE

KD of Spin1 in MII-stage porcine oocytes reduced metaphase-promoting factor and mitogen-activated protein kinase activities, resulting in spontaneous pronuclear formation without calcium activation. However, the DNA damage response was triggered by Spin1 overexpression, generating the checkpoint protein γH2A.X. Furthermore, Spin1 overexpression blocked metaphase-anaphase transition and led to multinucleation in oocytes and embryos.

LARGE SCALE DATA

None.

LIMITATIONS, REASONS FOR CAUTION: This study is based on in vitro investigations with abnormal expression levels of Spin1. This may or may not accurately reflect the situation in vivo.

WIDER IMPLICATIONS OF THE FINDINGS

Spin1 is essential to maintain MII arrest, but a high level of Spin1 induces DNA damage in oocytes and embryos. Thus, a system to accurately regulate Spin1 expression operates in porcine MII-stage oocytes and embryos.

STUDY FUNDING AND COMPETING INTEREST(S): This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (No. 2015R1D1A1A01057629). The authors declare no competing financial interests.

摘要

研究问题

纺锤体相关蛋白1(Spin1)在猪的中期II期卵母细胞中起什么作用?

总结答案

Spin1的缺失会诱导卵母细胞自发激活,而Spin1的过表达会通过诱导猪卵母细胞中的DNA损伤导致多核形成。

已知信息

关于Spin1在卵母细胞和胚胎中的功能知之甚少。在小鼠卵母细胞中,Spin1在配子发生过程中特异性表达,对减数分裂恢复至关重要。在体细胞中,Spin1促进癌细胞增殖并激活WNT/ T细胞因子信号传导。

研究设计、规模、持续时间:在猪的MII期卵母细胞中敲低(KD)或过表达Spin1后,额外培养24小时后检查MII期的维持情况。对孤雌胚胎进行培养,直至四细胞(72小时)或囊胚(7天)阶段。

参与者/材料、环境、方法:通过显微注射针对猪Spin1的siRNA,在猪卵母细胞和胚胎中敲低Spin1。为了过表达Spin1,构建了猪Spin1-eGFP的cRNA。此外,为了进行拯救实验,将编码抗siRNA的小鼠Spin1的cRNA添加到针对猪Spin1的siRNA中。对于过表达和拯救实验,使用与KD实验相同的方法进行显微注射和培养。

主要结果及机遇的作用

在MII期猪卵母细胞中敲低Spin1会降低促成熟因子和丝裂原活化蛋白激酶的活性,导致在无钙激活的情况下自发形成原核。然而,Spin1的过表达会触发DNA损伤反应,产生检查点蛋白γH2A.X。此外,Spin1的过表达会阻断中期-后期转换,并导致卵母细胞和胚胎中的多核形成。

大规模数据

无。

局限性、谨慎的原因:本研究基于对Spin1异常表达水平的体外研究。这可能准确反映体内情况,也可能不准确。

研究结果的更广泛影响

Spin1对于维持MII期阻滞至关重要,但高水平的Spin1会诱导卵母细胞和胚胎中的DNA损伤。因此,在猪的MII期卵母细胞和胚胎中存在一个精确调节Spin1表达的系统。

研究资金和竞争利益

本研究得到了韩国国家研究基金会(NRF)通过教育部资助的基础科学研究计划的支持(编号2015R1D1A1A01057629)。作者声明没有竞争财务利益。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验