Suppr超能文献

猪卵巢衰老过程中 DNA 甲基化和转录组表达的动态变化。

Dynamic Changes of DNA Methylation and Transcriptome Expression in Porcine Ovaries during Aging.

机构信息

Department of Zoology, College of Life Science, Sichuan Agricultural University, Ya'an, Sichuan 625014, China.

Sichuan Weimu Modern Agricultural Science and Technology Co., Ltd., Chengdu, Sichuan 611536, China.

出版信息

Biomed Res Int. 2019 Oct 30;2019:8732023. doi: 10.1155/2019/8732023. eCollection 2019.

Abstract

The biological function of human ovaries declines along with aging. To identify the underlying molecular changes during ovarian aging, pigs were used as model animals. Genome-wide DNA methylation and transcriptome-wide RNA expression analyses were performed via high-throughput sequencing of ovaries from young pigs (180 days, puberty stage of first ovulation) and old pigs (eight years, reproductive exhaustion stage). The results identified 422 different methylation regions between old and young pigs; furthermore, a total of 2,243 mRNAs, 95 microRNAs, 248 long noncoding RNAs (lncRNAs), and 116 circular RNAs (circRNAs) were differentially expressed during both developmental stages. Gene ontology analysis showed that these genes related to different methylation and expression are involved in the ovarian aging cycle. Specifically, these are involved in cell apoptosis, death effector domain binding, embryonic development, reproduction and fertilization process, ovarian cumulus expansion, and the ovulation cycle. Multigroup cooperative control relationships were also assessed, and competing endogenous RNA (ceRNA) networks were constructed in the ovarian aging cycle. These data will help to clarify ovary age-associated potential molecular changes in DNA methylation and transcriptional patterns over time.

摘要

人类卵巢的生物学功能随着年龄的增长而下降。为了确定卵巢衰老过程中的潜在分子变化,我们选择猪作为模型动物。通过对青年猪(180 天,第一次排卵的青春期阶段)和老年猪(8 岁,生殖衰竭阶段)的卵巢进行高通量测序,进行了全基因组 DNA 甲基化和转录组 RNA 表达的全基因组分析。结果在老年和青年猪之间鉴定出 422 个不同的甲基化区域;此外,在这两个发育阶段,共有 2243 个 mRNA、95 个 microRNA、248 个长链非编码 RNA(lncRNA)和 116 个环状 RNA(circRNA)差异表达。基因本体分析表明,这些与不同甲基化和表达相关的基因参与了卵巢衰老周期。具体来说,这些基因涉及细胞凋亡、死亡效应结构域结合、胚胎发育、生殖和受精过程、卵巢卵丘扩展和排卵周期。还评估了多组协同控制关系,并在卵巢衰老周期中构建了竞争内源性 RNA(ceRNA)网络。这些数据将有助于阐明卵巢年龄相关的潜在分子变化在 DNA 甲基化和转录模式随时间的变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef00/6874880/9a3d636809bb/BMRI2019-8732023.001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验