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Series GSE79030 Query DataSets for GSE79030
Status Public on Dec 21, 2016
Title KSHV Infection Mimics the Hypoxic Response Based on Next-Generation Sequencing [miRNA-Seq]
Platform organism Homo sapiens
Sample organisms Homo sapiens; Human gammaherpesvirus 8
Experiment type Non-coding RNA profiling by high throughput sequencing
Summary Purpose: Kaposi’s sarcoma associated-herpesvirus (KSHV) causes several hyperproliferative disorders, including Kaposi’s sarcoma, primary effusion lymphoma and multicentric Castleman’s disease. KSHV encodes for a number of microRNAs (miRNAs), and KSHV infection can affect the expression of cellular miRNAs. Hypoxia has been shown to induce KSHV reactivation, directly induce several KSHV lytic genes, and also induce the most abundant latent viral protein, LANA. Also, several KSHV proteins can stabilize and increase the cellular levels of hypoxia-inducible factor (HIF-1α). However, the degree to which hypoxic pathways are utilized by KSHV has yet to be determined.
Methods: We investigated the interplay between hypoxia and KSHV infection by comparing the 31effects of hypoxia and KSHV infection on miRNA and mRNA expression, and by examining the 32effects of hypoxia on uninfected and KSHV-infected cells. This was accomplished using next-33generation sequencing (NGS), qRT-PCR, Taqman assays, and pathway analysis.
Results: NGS analysis of human mRNAs revealed striking similarities (~34%) between the transcriptomic response to hypoxia and the transcriptomic response to KSHV infection. Additionally, hsa-miR-210, a key hypoxia-inducible miRNA with pro-angiogenic and anti-apoptotic properties, was found significantly up-regulated by both KSHV infection and hypoxia using Taqman assays. Finally, KSHV infected cells differed somewhat in their response to hypoxia compared to KSHV-uninfected controls.
Conclusions: These results demonstrate that KSHV harnesses a part of the hypoxic cellular response and induces miR-210 up-regulation. The understanding of how these miRNAs, genes and pathways are regulated by HIF-1α and KSHV infection are essential to a better understanding of the biology of KSHV-associated diseases.
 
Overall design 6 samples analyzed. Two experimental conditions: hypoxic uninfected cells (SLK cells) and hypoxic chronically KSHV-infected cells (SLKK cells) (n=3). Two sequencing platforms: microRNA-Seq and mRNA-Seq.
This hypoxia study was compared to a previously published normoxia study available on GEO (GSE62830).
 
Contributor(s) Coralie V, Robert Y, Jiannis R, Martin R
Citation(s) 28046107
Submission date Mar 09, 2016
Last update date May 15, 2019
Contact name Coralie Viollet
Organization name NIH/NCI
Street address 10 Center Dr
City Bethesda
State/province MD
ZIP/Postal code 20814
Country USA
 
Platforms (1)
GPL11154 Illumina HiSeq 2000 (Homo sapiens)
Samples (6)
GSM2084204 SLK_hypoxia_microRNAseq_rep1 [microRNA]
GSM2084205 SLK_hypoxia_microRNAseq_rep2 [microRNA]
GSM2084206 SLK_hypoxia_microRNAseq_rep3 [microRNA]
This SubSeries is part of SuperSeries:
GSE79032 RNA Sequencing Reveals that Kaposi Sarcoma-Associated Herpesvirus Infection Mimics Hypoxia Gene Expression Signature
Relations
Reanalysis of GSM1534016
Reanalysis of GSM1534017
Reanalysis of GSM1534018
Reanalysis of GSM1534019
Reanalysis of GSM1534020
Reanalysis of GSM1534021
BioProject PRJNA314773
SRA SRP071334

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Supplementary file Size Download File type/resource
GSE79030_RAW.tar 830.0 Kb (http)(custom) TAR (of BEDGRAPH)
GSE79030_hg19-mat-hyp-vs-norm-statsSLK.csv.gz 36.4 Kb (ftp)(http) CSV
GSE79030_hg19-mat-hyp-vs-norm-statsSLKK.csv.gz 31.1 Kb (ftp)(http) CSV
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Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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