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RNA-Sequencing Analysis of 5' Capped RNAs Identifies Many New Differentially Expressed Genes in Acute Hepatitis C Virus Infection (CROSBI ID 184449)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Papic, Neven ; Maxwell, Christopher ; Delker, Don ; Liu, Shuanghu ; Heale, Bret ; Hagedorn, Curt RNA-Sequencing Analysis of 5' Capped RNAs Identifies Many New Differentially Expressed Genes in Acute Hepatitis C Virus Infection // Viruses, 4 (2012), 4; 581-612. doi: 10.3390/v4040581

Podaci o odgovornosti

Papic, Neven ; Maxwell, Christopher ; Delker, Don ; Liu, Shuanghu ; Heale, Bret ; Hagedorn, Curt

engleski

RNA-Sequencing Analysis of 5' Capped RNAs Identifies Many New Differentially Expressed Genes in Acute Hepatitis C Virus Infection

We describe the first report of RNA sequencing of 5' capped (Pol II) RNAs isolated from acutely hepatitis C virus (HCV) infected Huh 7.5 cells that provides a general approach to identifying differentially expressed annotated and unannotated genes that participate in viral-host interactions. We identified 100, 684, and 1, 844 significantly differentially expressed annotated genes in acutely infected proliferative Huh 7.5 cells at 6, 48, and 72 hours, respectively (fold change ≥ 1.5 and Bonferroni adjusted p-values < 0.05). Most of the differentially expressed genes (>80%) and biological pathways (such as adipocytokine, Notch, Hedgehog and NOD-like receptor signaling) were not identified by previous gene array studies. These genes are critical components of host immune, inflammatory and oncogenic pathways and provide new information regarding changes that may benefit the virus or mediate HCV induced pathology. RNAi knockdown studies of newly identified highly upregulated FUT1 and KLHDC7B genes provide evidence that their gene products regulate and facilitate HCV replication in hepatocytes. Our approach also identified novel Pol II unannotated transcripts that were upregulated. Results further identify new pathways that regulate HCV replication in hepatocytes and suggest that our approach will have general applications in studying viral-host interactions in model systems and clinical biospecimens.

HCV; JFH-1; RNA-seq; gene expression; next generation sequencing; 5' cap; Huh 7.5; FUT1; KLHDC7B

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Podaci o izdanju

4 (4)

2012.

581-612

objavljeno

1999-4915

10.3390/v4040581

Povezanost rada

Temeljne medicinske znanosti, Kliničke medicinske znanosti, Biologija

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