Guangxi Key Laboratory of Animal Breeding, Disease Control and Prevention, College of Animal Science & Technology, Guangxi University, Nanning, Guangxi 530004, China.
Kunpeng Institute of Modern Agriculture at Foshan, Agricultural Genomics Institute, Chinese Academy of Agricultural Sciences, Foshan 528226, China.
G3 (Bethesda). 2024 Oct 7;14(10). doi: 10.1093/g3journal/jkae178.
RNA editing is a co-transcriptional/post-transcriptional modification that is mediated by the ADAR enzyme family. Profiling of RNA editing is very limited in pigs. In this study, we collated 3813 RNA-seq data from the public repositories across 23 tissues and carried out comprehensive profiling of RNA editing in pigs. In total, 127,927 A-to-I RNA-editing sites were detected. Our analysis showed that 98.2% of RNA-editing sites were located within repeat regions, primarily within the pig-specific SINE retrotransposon PRE-1/Pre0_SS elements. Subsequently, we focused on analyzing specific RNA-editing sites (SESs) in skeletal muscle tissues. Functional enrichment analyses suggested that they were enriched in signaling pathways associated with muscle cell differentiation, including DMD, MYOD1, and CAV1 genes. Furthermore, we discovered that RNA editing event in the 3'UTR of CFLAR mRNA influenced miR-708-5p binding in this region. In this study, the panoramic RNA-editing landscape of different tissues of pigs was systematically mapped, and RNA-editing sites and genes involved in muscle cell differentiation were identified. In summary, we identified modifications to pig RNA-editing sites and provided candidate targets for further validation.
RNA 编辑是一种共转录/转录后修饰,由 ADAR 酶家族介导。猪的 RNA 编辑谱分析非常有限。在这项研究中,我们整理了来自 23 个组织的公共存储库中的 3813 个 RNA-seq 数据,并对猪的 RNA 编辑进行了全面分析。总共检测到 127927 个 A-to-I RNA 编辑位点。我们的分析表明,98.2%的 RNA 编辑位点位于重复区域内,主要位于猪特异性 SINE 反转录转座子 PRE-1/Pre0_SS 元件内。随后,我们专注于分析骨骼肌组织中的特定 RNA 编辑位点(SESs)。功能富集分析表明,它们富集在与肌肉细胞分化相关的信号通路中,包括 DMD、MYOD1 和 CAV1 基因。此外,我们发现 CFLAR mRNA 3'UTR 中的 RNA 编辑事件影响了该区域 miR-708-5p 的结合。在这项研究中,系统地绘制了不同组织的猪全景 RNA 编辑图谱,并鉴定了参与肌肉细胞分化的 RNA 编辑位点和基因。总之,我们鉴定了猪 RNA 编辑位点的修饰,并提供了候选靶标进行进一步验证。