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Series GSE242551 Query DataSets for GSE242551
Status Public on Sep 12, 2023
Title Effects of Rift Valley fever virus infection on gene expression and alternative splicing in HEK 293 cells
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Rift Valley fever virus (RVFV) is an important human and livestock pathogen. To better understand the molecular virology and mechanisms of pathogenesis in human HEK293 cells during RVFV MP-12 strain infection, we used high-throughput mRNA sequencing technology to identify and analyze differentially expressed genes and mRNA splicing patterns triggered by infection or by expression of RVFV nucleocapsid protein. Here we supply the results of our RNA-seq analysis of RVFV-infected cells and cells transfected with RVFV nucleocapsid protein expressing plasmids. Some of the results were published in: "Transcriptome profiling in Rift Valley fever virus infected cells reveals modified transcriptional and alternative splicing programs" by Katherine E Havranek, Luke Adam White, Jean-Marc Lanchy, J Stephen Lodmell. PLoS One. 2019 May 28;14(5):e0217497. PMID: 31136639 PMCID: PMC6538246.
 
Overall design To investigate the impact of Rift Valley Fever Virus (RVFV) infection on human gene expression and alternative splicing patterns, we infected HEK cells with RVFV MP12 strain and harvested total RNA two days post-infection. The transcript expression levels and alternative splicing events were measured by the analysis of 150-bp Illumina sequencing paired-reads of the purified polydenylated RNAs. We also analyzed, using the same Illumina sequencing technique, the impact heterologous expression of the viral RNA-binding N protein on host gene expression levels and alternative splicing events. The HEK293 cells used in that experiment were transfected with a viral N protein expression plasmid and the total RNA was harvested two days after the transfection and the purified polydenylated RNAs were processed for Illumina sequencing.
 
Contributor(s) Havranek KE, White LA, Lanchy J, Lodmell JS
Citation(s) 31136639
Submission date Sep 07, 2023
Last update date Dec 12, 2023
Contact name J Stephen Lodmell
E-mail(s) stephen.lodmell@mso.umt.edu
Phone 406 243-6393
Organization name The University of Montana
Department Biological Sciences
Lab Lodmell
Street address 32 campus drive
City Missoula
State/province MT
ZIP/Postal code 59812
Country USA
 
Platforms (1)
GPL11154 Illumina HiSeq 2000 (Homo sapiens)
Samples (9)
GSM7765966 HEK293 cells, Mock infection, day 2, replicate 1
GSM7765967 HEK293 cells, Mock infection, day 2, replicate 2
GSM7765968 HEK293 cells, Mock infection, day 2, replicate 3
Relations
BioProject PRJNA1013925

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
GSE242551_A3SS.miso_summary.txt.gz 305.8 Kb (ftp)(http) TXT
GSE242551_A5SS.miso_summary.txt.gz 217.7 Kb (ftp)(http) TXT
GSE242551_MP_12_vs_Mock.miso_bf.filtered.xlsx 243.9 Kb (ftp)(http) XLSX
GSE242551_MP_12vsMock.DEG.fasta.gz 15.9 Mb (ftp)(http) FASTA
GSE242551_MP_12vsMock.DEG.txt.gz 946.4 Kb (ftp)(http) TXT
GSE242551_MXE.miso_summary.txt.gz 210.9 Kb (ftp)(http) TXT
GSE242551_N_vs_MP_12.miso_bf.filtered.xlsx 260.4 Kb (ftp)(http) XLSX
GSE242551_N_vs_Mock.miso_bf.filtered.xlsx 107.5 Kb (ftp)(http) XLSX
GSE242551_NvsMP_12.DEG.fasta.gz 15.5 Mb (ftp)(http) FASTA
GSE242551_NvsMP_12.DEG.txt.gz 926.4 Kb (ftp)(http) TXT
GSE242551_NvsMock.DEG.fasta.gz 8.1 Mb (ftp)(http) FASTA
GSE242551_NvsMock.DEG.txt.gz 422.2 Kb (ftp)(http) TXT
GSE242551_RI.miso_summary.txt.gz 161.8 Kb (ftp)(http) TXT
GSE242551_SE.miso_summary.txt.gz 1006.4 Kb (ftp)(http) TXT
GSE242551_fpkm.txt.gz 2.1 Mb (ftp)(http) TXT
GSE242551_readcount.txt.gz 616.0 Kb (ftp)(http) TXT
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