畜牧与饲料科学 ›› 2021, Vol. 42 ›› Issue (4): 37-41.doi: 10.12160/j.issn.1672-5190.2021.04.007

• 动物遗传与繁育 • 上一篇    下一篇

绵羊不同妊娠时期卵巢转录组差异表达比较分析

史静茹1,2, 郭丽丽1,2, 刘在霞1,2, 刘永斌3, 张家新1,2, 张文广1,2   

  1. 1.内蒙古农业大学动物科学学院,内蒙古 呼和浩特 010018;
    2.动物遗传育种与繁殖内蒙古自治区重点实验室,内蒙古 呼和浩特 010018;
    3.内蒙古自治区农牧业科学院,内蒙古 呼和浩特 010031
  • 收稿日期:2021-03-11 出版日期:2021-07-30 发布日期:2021-08-25
  • 通讯作者: 张家新(1970—),男,教授,博士,博士生导师,主要研究方向为家畜繁殖生物学与繁殖技术。张文广(1973—),男,教授,博士,博士生导师,主要研究方向为数量基因组学与性状遗传机理。
  • 作者简介:史静茹(1995—),女,硕士研究生,主要研究方向为数量基因组学与性状遗传机理。

Comparative Transcriptomic Analysis to Identify Differentially Expressed Genes in Sheep Ovaries during Different Periods of Gestation

SHI Jing-ru1,2, GUO Li-li1,2, LIU Zai-xia1,2, LIU Yong-bin3, ZHANG Jia-xin1,2, ZHANG Wen-guang1,2   

  1. 1. College of Animal Science,Inner Mongolia Agricultural University,Hohhot 010018,China;
    2. Inner Mongolia Key Laboratory of Animal Genetics,Breeding and Reproduction,Hohhot 010018,China;
    3. Inner Mongolia Academy of Agricultural and Animal Husbandry Sciences,Hohhot 010031,China
  • Received:2021-03-11 Online:2021-07-30 Published:2021-08-25

摘要: [目的]探究随着绵羊体内胎儿的发育,母体卵巢转录组表达水平的变化。[方法]试验绵羊为苏格兰黑面羊和特克赛尔羊F1代杂交品种,3个妊娠时间分别为妊娠23 d、妊娠35 d和妊娠100 d。从NCBI的高通量测序数据SRA存储库下载3个妊娠时期绵羊卵巢转录组的18个样本数据。使用Z-Score方法对转录组数据进行标准化处理。将妊娠23 d、妊娠35 d的绵羊卵巢组织进行比对,妊娠35 d、妊娠100 d的绵羊卵巢组织进行比对,使用R语言的limma包进行基因差异表达分析,筛选DEGs,以P-Value<0.05和|logFC|≥2作为筛选DEGs条件。利用DAVID在线软件对DEGs进行注释及功能富集分析,并以P-Value<0.05作为信号通路显著富集标志。[结果]在妊娠23 d与妊娠35 d组绵羊卵巢中筛选出54个DEGs,妊娠35 d与妊娠100 d组绵羊卵巢中筛选出68个DEGs,两组均包含HSP90AA1、HSP90AB1、MMP2和HSP90B1基因。妊娠23 d与35 d组绵羊卵巢的54个DEGs显著富集到包括内质网蛋白质加工信号通路、核糖体信号通路、雌激素信号通路、癌症蛋白聚糖信号通路、扩张型心肌病信号通路、肥厚型心肌病信号通路6条通路;妊娠35 d、妊娠100 d组绵羊卵巢的68个DEGs显著富集到包括癌症相关信号通路、黏着斑信号通路、抗原加工与提呈信号通路、细胞外基质受体相互作用信号通路、细菌侵袭上皮细胞信号通路、内质网蛋白质加工信号通路、核糖体信号通路、雌激素信号通路、PI3K-Akt信号通路、癌症蛋白聚糖信号通路和前列腺癌信号通路11条通路。[结论]在妊娠期间雌激素信号通路上的HSP90AA1、HSP90AB1、MMP2和HSP90B1基因表达有很大变化,这些基因可能对绵羊妊娠维持有着重要的作用。

关键词: 绵羊, 转录组, 妊娠, 卵巢

Abstract: [Objective] To transcriptomically identify the differentially expressed genes (DEGs) in maternal ovary with the development of fetus in sheep. [Method] F1 hybrids of Scottish black-faced sheep and Texel sheep were used as experimental animals, and the transcriptomic analysis profiles were collected on 23th day, 35th day and 100th day of gestation, respectively. A total of 18 transcriptomic data samples of sheep ovaries in the above three periods of gestation were downloaded from SRA in NCBI, a high-throughput sequencing data storing database. The transcriptomic data were standardized using Z-Score method. Comparative transcriptomic analysis was carried out between 23th day and 35th day of gestation as well as between 35th day and 100th day of gestation. The limma package of R language was used for analysis of differential gene expression to screen DEGs, and P-Value < 0.05 and |logFC| ≥ 2 were used as screening conditions for DEGs. DAVID online software was used to annotate DEGs and analyze their functional enrichment, and P-Value < 0.05 was used as a significant enrichment marker of signaling pathway. [Result]A total of 54 DEGs in sheep ovaries were screened between 23th day and 35th day of gestation, and a total of 68 DEGs were screened between 35th day and 100th day of gestation. The genes of HSP90AA1,HSP90AB1,MMP2 and HSP90B1 were observed in both groups of the DEGs. The 54 DEGs identified between 23th day and 35th day of gestation were found to be significantly enriched in six signaling pathways, including protein processing in endoplasmic reticulum, ribosome, estrogen, proteoglycans in cancer, dilated cardiomyopathy, and hypertrophic cardiomyopathy. The 68 DEGs identified between 35th day and 100th day of gestation were found to be significantly enriched in eleven signaling pathways, including cancer, focal adhesion, antigen processing and presentation, extracellular matrix (ECM)-receptor interaction, bacterial invasion of epithelial cells, protein processing in endoplasmic reticulum, ribosome, estrogen, PI3K-Akt, proteoglycans in cancer, and prostate cancer. [Conclusion] The gene expressions of HSP90AA1、HSP90AB1、MMP2 and HSP90B1 in estrogen signaling pathway during gestation have significant changes, indicating that these genes may play important roles in sheep gestation maintenance.

Key words: sheep, transcriptome, gestation, ovary

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