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Downregulation of IRF4 induces lytic reactivation of KSHV in primary effusion lymphoma cells.


ABSTRACT: Primary effusion lymphoma (PEL), associated with the latent infection by KSHV, constitutively expresses interferon-regulatory factor 4 (IRF4). We recently showed that IRF4 differentially regulates expression of cellular interferon-stimulated genes (ISGs) and viral genes (Forero et al., 2013). Here, using inducible IRF4 knockdown, we demonstrate that IRF4 silencing results in enhanced transcription of KSHV replication transactivator RTA. As a result viral transcription is increased leading to virus reactivation. Taken together, our results show that IRF4 helps maintain the balance between latency and KSHV reactivation in PEL cells.

SUBMITTER: Forero A 

PROVIDER: S-EPMC4058074 | biostudies-literature | 2014 Jun

REPOSITORIES: biostudies-literature

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Downregulation of IRF4 induces lytic reactivation of KSHV in primary effusion lymphoma cells.

Forero Adriana A   McCormick Kevin D KD   Jenkins Frank J FJ   Sarkar Saumendra N SN  

Virology 20140505


Primary effusion lymphoma (PEL), associated with the latent infection by KSHV, constitutively expresses interferon-regulatory factor 4 (IRF4). We recently showed that IRF4 differentially regulates expression of cellular interferon-stimulated genes (ISGs) and viral genes (Forero et al., 2013). Here, using inducible IRF4 knockdown, we demonstrate that IRF4 silencing results in enhanced transcription of KSHV replication transactivator RTA. As a result viral transcription is increased leading to vir  ...[more]

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