畜牧兽医学报 ›› 2024, Vol. 55 ›› Issue (2): 576-586.doi: 10.11843/j.issn.0366-6964.2024.02.015

• 生物技术与繁殖 • 上一篇    下一篇

猪卵泡液外泌体处理卵巢颗粒细胞的SNP/Indel筛选分析

刘阳光, 章会斌, 文浩宇, 谢帆, 赵世明, 丁月云, 郑先瑞, 殷宗俊*, 张晓东*   

  1. 安徽农业大学动物科技学院, 合肥 230036
  • 收稿日期:2023-08-02 出版日期:2024-02-23 发布日期:2024-02-27
  • 通讯作者: 殷宗俊,主要从事动物遗传育种研究,E-mail:yinzongjun@ahau.edu.cn;张晓东,主要从事动物遗传育种研究,E-mail:xdzhang1983@163.com
  • 作者简介:刘阳光(1997-),男,安徽阜阳人,博士生,主要从事动物遗传育种研究,E-mail:22710033@stu.ahau.edu.cn
  • 基金资助:
    国家自然科学基金(31972531);安徽省高校协同创新项目(GXXT-2021-055);国家重点研发计划(2021YFD1301200);安徽省科技重大专项(202103a06020013)

SNP/Indel Screening Analysis of Porcine Ovarian Granulosa Cells Treated with Follicular Fluid Exosomes

LIU Yangguang, ZHANG Huibin, WEN Haoyu, XIE Fan, ZHAO Shiming, DING Yueyun, ZHENG Xianrui, YIN Zongjun*, ZHANG Xiaodong*   

  1. College of Animal Science and Technology, Anhui Agricultural University, Hefei 230036, China
  • Received:2023-08-02 Online:2024-02-23 Published:2024-02-27

摘要: 旨在分析卵泡液外泌体对卵巢颗粒细胞基因的影响,了解卵泡液外泌体在卵泡发育过程中的调控机理,为母猪繁殖研究提供理论依据。本研究选取6月龄、健康状态良好且体重相近的二元母猪为材料,屠宰后收集卵巢150枚,利用梯度离心法获取卵泡液外泌体与猪卵巢颗粒细胞(porcine ovarian granulosa cells,POGCs),并在体外将卵泡液外泌体与猪卵巢颗粒细胞共培养。通过RNA-seq技术对猪卵巢颗粒细胞(granulosa cell samples,GC,n=3)和与外泌体共培养的猪卵巢颗粒细胞(granulosa-exosome co-culture samples,GCE,n=3)进行测序。结果显示,在GC和GCE组中平均每个样品获得5.54×107 条clean reads,Q20和Q30质量得分均在92%以上。在GC和GCE组的6个样品中共获得1 310 979个SNPs突变和104 498个InDel突变,其中纯合型SNP/Indel突变数量为170 426个,杂合型SNP/Indel突变数量为1 245 052个,突变杂合子数目明显高于纯合子且SNP的发生率较高。另外,在突变类型中,转换类型共计973 003个,颠换类型339 974个,转换的类型显著高于颠换类型。经基因注释,突变主要发生在基因3'UTR、5'UTR、内含子区域,其次为外显子和基因间隔区。另外,通过与差异基因对比后,够筛选出1 583个候选基因,经GO和KEGG功能富集发现,候选基因主要与细胞周期以及细胞增殖/凋亡过程相关。此外,共发现14个与细胞周期、增殖/凋亡通路相关的关键候选基因,其中11个基因存在互作关系。本研究获得的这些SNP/Indel信息可为后续研究外泌体在母猪生殖上的调控奠定科学基础。

关键词: 猪, 卵泡液外泌体, 卵巢颗粒细胞, SNP, RNA-seq

Abstract: The aim of this study was to analyze the effect of follicular fluid exosomes on the genes of ovarian granulosa cells, to understand the regulation mechanism of follicular fluid exosomes during follicular development, and to provide a theoretical basis for the study of sow reproduction. In this study, 6-month-old binary sows with good health status and similar body weight were selected as experimental materials, and 150 ovaries were collected after slaughter, and follicular fluid exosomes and porcine ovarian granulosa cells (POGCs) were obtained using gradient centrifugation, and follicular fluid exosomes and porcine ovarian granulosa cells was co-cultured in vitro. Porcine ovarian granulosa cells (granulosa cell samples, GC, n=3) and porcine ovarian granulosa cells co-cultured with exosomes (granulosa-exosome co-culture samples, GCE, n=3) were sequenced by RNA-seq. The results showed that an average of 5.54×107 clean reads were obtained per sample in the GC and GCE groups, and the Q20 and Q30 quality scores were greater than 92%. A total of 1 310 979 SNP mutations and 104 498 InDel mutations were obtained in 6 samples in the GC and GCE groups, among which the number of homozygous SNP/Indel mutations was 170 426 and the number of heterozygous SNP/Indel mutations was 1 245 052, and the number of mutant heterozygotes was significantly higher than the number of homozygotes and with a high incidence of SNPs. In addition, among the mutation types, there were 973 003 transformations and 339 974 transversion, and the number of transformations was significantly higher than the number of transversion. After gene annotation, the mutations mainly occurred in the 3'UTR, 5'UTR, and intron regions of the genes, followed by exons and intergenic regions. In addition, after comparison with the differential genes, the 1 583 candidate genes were screened, and it was found by GO and KEGG functional enrichment that the candidate genes were mainly related to cell cycle and cell proliferation/apoptosis processes. In addition, a total of 14 key candidate genes related to cell cycle and proliferation/apoptosis pathways were identified, of which 11 genes had interaction relationships. These SNP/Indel information obtained in this study can provide a scientific basis for subsequent studies on the regulation of exosomes on sow reproduction.

Key words: pig, follicular fluid exosomes, ovarian granulosa cells, SNP, RNA-seq

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