畜牧兽医学报 ›› 2023, Vol. 54 ›› Issue (12): 5066-5076.doi: 10.11843/j.issn.0366-6964.2023.12.017

• 生物技术与繁殖 • 上一篇    下一篇

绵羊miR-200b启动子鉴定及其对卵泡颗粒细胞线粒体功能的影响

宋鹏琰1, 王思伟1,2, 岳巧娴1, 张寅梁1, 陈晓勇1, 周荣艳1*   

  1. 1. 河北农业大学动物科技学院, 保定 071001;
    2. 河北省农林科学院粮油作物研究所, 石家庄 050035
  • 收稿日期:2023-05-24 出版日期:2023-12-23 发布日期:2023-12-26
  • 通讯作者: 周荣艳,主要从事动物遗传育种与繁殖研究,Tel:0312-7528451,E-mail:rongyanzhou@126.com
  • 作者简介:宋鹏琰(1992-),女,河北邢台人,博士生,主要从事动物遗传育种与繁殖研究,E-mail:spy1509@163.com
  • 基金资助:
    河北农业大学精准畜牧学科群建设项目(1090064);河北省科学自然科学基金项目(C2019204039)

Identification of oar-miR-200b Promoter and Effects on Mitochondrial Function in Follicular Granulosa Cells

SONG Pengyan1, WANG Siwei1,2, YUE Qiaoxian1, ZHANG Yinliang1, CHEN Xiaoyong1, ZHOU Rongyan1*   

  1. 1. College of Animal Science and Technology, Hebei Agricultural University, Baoding 071001, China;
    2. Institute of Cereal and Oil Crops, Hebei Academy of Agriculture and Forestry Sciences, Shijiazhuang 050035, China
  • Received:2023-05-24 Online:2023-12-23 Published:2023-12-26

摘要: 旨在鉴定绵羊miR-200b的启动子区并研究其对卵泡颗粒细胞线粒体功能的影响。本研究体外分离培养绵羊卵泡颗粒细胞,通过构建包含3个不同长度启动子区重组质粒,利用生物信息软件和双荧光素酶报告试验预测并鉴定绵羊miR-200b核心启动子区;利用在线工具预测转录因子NR4A1的结合位点;通过双荧光素酶报告试验和qRT-PCR检测过表达NR4A1基因对miR-200b启动子活性和表达水平的影响;通过转染miR-200b mimic和mimic NC,分别检测颗粒细胞线粒体形态和数量、线粒体膜电位、ROS水平、ATP和线粒体呼吸链复合物 Ⅰ 的浓度,并检测线粒体氧化磷酸化相关基因表达水平。结果表明,miR-200b-P1(-159/+36 nt)活性最高,确定该区域为miR-200b核心启动子区;预测出核心启动子存在1个NR4A1的结合位点,且过表达NR4A1基因显著上调miR-200b启动子活性和miR-200b的表达水平(P<0.01)。与mimic NC组相比,转染miR-200b mimic导致颗粒细胞平均光密度显著降低(P<0.01),细胞长度显著缩短(P<0.01)、线粒体膜电位下降(P<0.05)、ATP(P<0.05)和线粒体呼吸链体复合物 Ⅰ (P<0.01)的浓度降低、ROS水平升高(P<0.01),同时下调ATP6V1G1和NDUFV1的表达(P<0.01),上调NOX4的表达水平(P<0.01)。该研究确定了绵羊miR-200b的核心启动子区(-159/+36 nt),NR4A1正向调控miR-200b的转录,且miR-200b能够影响线粒体氧化磷酸化过程,诱导颗粒细胞线粒体损伤。该研究结果为进一步揭示miR-200b调控绵羊卵泡发育的机制提供了理论依据。

关键词: 绵羊, miR-200b, 启动子, 卵泡颗粒细胞, 线粒体

Abstract: The purpose of this study was to identify the oar-miR-200b promoter and investigate the effects of miR-200b on mitochondrial function in follicular granulosa cells. Sheep ovarian follicular granulosa cells were isolated and cultured in vitro, recombinant plasmids containing 3 different lengths of promoter region were constructed, and bioinformatics software and dual-luciferase reporting assays were used to predict and identify the oar-miR-200b core promoter region. Online tools were used to predict the binding site of transcription factor NR4A1, and the effect of overexpression of NR4A1 gene on miR-200b promoter activity and expression levels was detected by dual-luciferase reporter assay and qRT-PCR. Mitochondrial morphology and number, mitochondrial membrane potential, ROS levels, the concentration of ATP and mitochondrial respiratory chain complex Ⅰ were respectively detected by transfection miR-200b mimic and mimic NC, respectively, and the expression levels of mitochondrial oxidative phosphorylation-related genes were detected. The result indicated that the highest activity of miR-200b-P1 (-159/+36 nt) was regarded as the core promoter region of miR-200b. There was one binding site of NR4A1 in the miR-200b core promoter. The miR-200b promoter activity and miR-200b expression increased in NR4A1 overexpressed cells (P<0.01). Compared with mimic NC group, transfection of miR-200b mimic resulted in a significant decrease in the mean optical density (P<0.01) and a reduction in cell length (P<0.01) of granulosa cells, decreased mitochondrial membrane potential (P<0.05), concentrations of ATP (P<0.05) and mitochondrial respiratory chain complex I (P<0.01), and increased ROS levels (P<0.01), accompany with down-regulating the expression of ATP6V1G1 and NDUFV1 (P<0.01) and up-regulating the expression level of NOX4 (P<0.01). This study determined the core promoter region of oar-miR-200b (-159/+36 nt), NR4A1 positively regulated the transcription of miR-200b, and miR-200b might affect the process of mitochondrial OXPHOS and induce mitochondrial damage in granulosa cells. These results provide a theoretical basis for further revealing the mechanism of miR-200b during sheep ovarian follicular development.

Key words: sheep, miR-200b, promoter, follicular granulosa cells, mitochondria

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