» Articles » PMID: 32083129

Global Analysis of Alternative Splicing Difference in Peripheral Immune Organs Between Tongcheng Pigs and Large White Pigs Artificially Infected with PRRSV

Overview
Journal Biomed Res Int
Publisher Wiley
Date 2020 Feb 22
PMID 32083129
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Alternative splicing (AS) plays a significant role in regulating gene expression at the transcriptional level in eukaryotes. Flexibility and diversity of transcriptome and proteome can be significantly increased through alternative splicing of genes. In the present study, transcriptome data of peripheral immune organs including spleen and inguinal lymph nodes (ILN) were used to identify AS difference between PRRSV-resistant Tongcheng (TC) pigs and PRRSV-susceptible Large White (LW) pigs artificially infected with porcine reproductive and respiratory syndrome virus (PRRSV) . The results showed that PRRSV infection induced global alternative splicing events (ASEs) with different modes. Among them, 373 genes and 595 genes in the spleen and ILN of TC pigs, while 458 genes and 560 genes in the spleen and ILN of LW pigs had significantly differential ASEs. Alternative splicing was subject to tissue-specific and lineage-specific regulation in response to PRRSV infection. Enriched GO terms and pathways showed that genes with differential ASEs played important roles in transcriptional regulation, immune response, metabolism, and apoptosis. Furthermore, a splicing factor associated with apoptosis, , was significantly upregulated in LW pigs. Functional analysis on apoptosis associated genes was validated by RT-PCR and DNA sequencing. These findings revealed different response to PRRSV between PRRSV-resistant TC pigs and PRRSV-susceptible LW pigs at the level of alternative splicing, suggesting the potential relationship between AS and disease resistance to PRRSV.

Citing Articles

Exploring Multi-Tissue Alternative Splicing and Skeletal Muscle Metabolism Regulation in Obese- and Lean-Type Pigs.

Wang W, Li W, Liu W, Wang Z, Xie B, Yang X Genes (Basel). 2024; 15(2).

PMID: 38397185 PMC: 10888101. DOI: 10.3390/genes15020196.


Genetic background influences pig responses to porcine reproductive and respiratory syndrome virus.

Pei Y, Lin C, Li H, Feng Z Front Vet Sci. 2023; 10:1289570.

PMID: 37929286 PMC: 10623566. DOI: 10.3389/fvets.2023.1289570.


Distinct traces of mixed ancestry in western commercial pig genomes following gene flow from Chinese indigenous breeds.

Peng Y, Derks M, Groenen M, Zhao Y, Bosse M Front Genet. 2023; 13:1070783.

PMID: 36712875 PMC: 9880450. DOI: 10.3389/fgene.2022.1070783.


Integrated analysis of lncRNA-mediated ceRNA network involved in immune regulation in the spleen of Meishan piglets.

Shi J, Xu C, Wu Z, Bao W, Wu S Front Vet Sci. 2022; 9:1031786.

PMID: 36337195 PMC: 9627291. DOI: 10.3389/fvets.2022.1031786.


Transcriptome profile of spleen tissues from locally-adapted Kenyan pigs (Sus scrofa) experimentally infected with three varying doses of a highly virulent African swine fever virus genotype IX isolate: Ken12/busia.1 (ken-1033).

Machuka E, Juma J, Muigai A, Amimo J, Pelle R, Abworo E BMC Genomics. 2022; 23(1):522.

PMID: 35854219 PMC: 9294756. DOI: 10.1186/s12864-022-08754-8.


References
1.
Montero H, Garcia-Roman R, Mora S . eIF4E as a control target for viruses. Viruses. 2015; 7(2):739-50. PMC: 4353914. DOI: 10.3390/v7020739. View

2.
Batra R, Stark T, Clark A, Belzile J, Wheeler E, Yee B . RNA-binding protein CPEB1 remodels host and viral RNA landscapes. Nat Struct Mol Biol. 2016; 23(12):1101-1110. PMC: 5140759. DOI: 10.1038/nsmb.3310. View

3.
Shkreta L, Chabot B . The RNA Splicing Response to DNA Damage. Biomolecules. 2015; 5(4):2935-77. PMC: 4693264. DOI: 10.3390/biom5042935. View

4.
Jiang Z, Zhou X, Michal J, Wu X, Zhang L, Zhang M . Reactomes of porcine alveolar macrophages infected with porcine reproductive and respiratory syndrome virus. PLoS One. 2013; 8(3):e59229. PMC: 3602036. DOI: 10.1371/journal.pone.0059229. View

5.
Wang P, Fung S, Gao W, Deng J, Cheng Y, Chaudhary V . A novel transcript isoform of STING that sequesters cGAMP and dominantly inhibits innate nucleic acid sensing. Nucleic Acids Res. 2018; 46(8):4054-4071. PMC: 5934658. DOI: 10.1093/nar/gky186. View