NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE149711 Query DataSets for GSE149711
Status Public on Jun 19, 2020
Title Identification of lncRNAs involved in the PCV2 infection of PK-15 cells
Organism Sus scrofa
Experiment type Expression profiling by high throughput sequencing
Summary Porcine circovirus type 2 (PCV2) can cause severe disease in the affected pigs, resulting in massive economic loss for the swine industry. Transcriptomics and proteomics approaches have been widely employed to identify the underlying molecular mechanisms of PCV2 infection. Numerous differentially expressed mRNAs, miRNAs, and proteins, together with their associated signaling pathways, have been identified, paving the way to further validation of their biological functions. Long non-coding RNA (lncRNA) is an important regulator of multiple biological processes. However, rare information regarding its role in the PCV2 infection has been obtained. Hence, in our study, RNA-seq was performed by infecting PK-15 cells with PCV2. Analysis of the differentially expressed genes (DEGs) suggested that cytoskeleton, apoptosis, cell division, and protein phosphorylation were significantly disturbed. Then, using stringent parameters, six lncRNAs were identified. Additionally, the potential targets of the lncRNAs were predicted using both cis- and trans-prediction methods. Interestingly, we found that the HOXB (Homeobox B) gene cluster was probably the target of the lncRNA LOC106505099. Enrichment analysis of the target genes showed that numerous developmental processes were altered during PCV2 infection. Therefore, our study revealed that lncRNAs could affect porcine embryo development through the regulation of the HOXB genes.
 
Overall design PK-15 cells were cultured in DMEM (Hyclone) with 10% FBS (Hyclone) in 6-well plates until reaching 80% confluency. Then, 3 wells of one plate were infected with Porcine Circovirus type 2 (PCV2) with MOI of 0.1. After 72 hours, the cells were harvested (3 PCV2-infection, 3 for mock infection) were harvested, subjected to total RNA extraction, and sequencing.
 
Contributor(s) He J, Wang H
Citation(s) 32560439
Submission date May 01, 2020
Last update date Jul 20, 2020
Contact name Jin He
E-mail(s) hejin@zju.edu.cn
Organization name Zhejiang University
Street address Yuhangtang Road No.866
City Hangzhou
ZIP/Postal code 310058
Country China
 
Platforms (1)
GPL22918 HiSeq X Ten (Sus scrofa)
Samples (6)
GSM4509252 con-1
GSM4509253 con-2
GSM4509254 con-3
Relations
BioProject PRJNA629788
SRA SRP259926

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE149711_Normalized_dataset.xls.gz 2.2 Mb (ftp)(http) XLS
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap