Biotechnology Bulletin ›› 2024, Vol. 40 ›› Issue (10): 288-295.doi: 10.13560/j.cnki.biotech.bull.1985.2024-0455

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Study on Constructing an RNA Editing Map of Pig Based on Large-scale RNA-seq Data

LONG Jia-jia1,2,3(), LIU Wei-wei1,2,3, FAN Xin-hao2,3,4, LI Wang-chang1, YANG Xiao-gan1, TANG Zhong-lin1,2,3,4()   

  1. 1. Guangxi Key Laboratory of Animal Breeding, Disease Control and Prevention, College of Animal Science & Technology, Guangxi University, Nanning 530004
    2. Kunpeng Institute of Modern Agriculture at Foshan, Foshan 528226
    3. Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Key Laboratory of Livestock and Poultry Multi-Omics of MARA, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen 518124
    4. Key Laboratory of Agricultural Animal Genetics, Breeding and Reproduction of Ministry of Education & Key Lab of Swine Genetics and Breeding of Ministry of Agriculture and Rural Affairs, Huazhong Agricultural University, Wuhan 430070
  • Received:2024-05-15 Online:2024-10-26 Published:2024-11-20
  • Contact: TANG Zhong-lin E-mail:2118301022@st.gxu.edu.cn;tangzhonglin@caas.cn

Abstract:

【Objective】 A-to-I RNA editing is a co-transcriptional/post-transcriptional modification mediated by the ADAR enzyme family. The systematic mapping of the RNA editome in pigs provided candidate targets for molecular breeding in pigs. 【Method】 We collected 3 461 RNA-seq datasets from 16 types of pig tissues and detected RNA editing sites in pigs using bioinformatics methods.【Result】 A total of 130 989 RNA editing sites were detected, of which 124 208 were A-to-I RNA editing sites. Analysis of the characteristics of the A-to-I RNA editing sites revealed that 98.2% were located in repetitive regions, primarily within the PRE-1/Pre0_SS elements of pig-specific SINE retrotransposons. Only 12.3% of A-to-I RNA editing sites had coding potential. Finally, the study analyzed tissue-specific A-to-I RNA editing sites in seven tissues(adipose, brain, large intestine, small intestine, skeletal muscle, liver, and lung). Functional enrichment analysis of the host genes in adipose tissue-specific sites showed that these genes were enriched in pathways related to cellular lipid metabolic processes, lipid metabolic processes, and thioester metabolic processes. Genes related to fat deposition within these pathways included PDK1, ACSL1 and PDE3B.【Conclusion】 This study comprehensively mapped the RNA editing sites in pigs, providing candidate targets for molecular breeding.

Key words: A-to-I RNA editing, fat deposition, pig, tissue, tissue-specific RNA editing sites