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PMID:22574148

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Citation

Austin, D, Baer, A, Lundberg, L, Shafagati, N, Schoonmaker, A, Narayanan, A, Popova, T, Panthier, JJ, Kashanchi, F, Bailey, C and Kehn-Hall, K (2012) p53 Activation following Rift Valley fever virus infection contributes to cell death and viral production. PLoS ONE 7:e36327

Abstract

Rift Valley fever virus (RVFV) is an emerging viral zoonosis that is responsible for devastating outbreaks among livestock and is capable of causing potentially fatal disease in humans. Studies have shown that upon infection, certain viruses have the capability of utilizing particular cellular signaling pathways to propagate viral infection. Activation of p53 is important for the DNA damage signaling cascade, initiation of apoptosis, cell cycle arrest and transcriptional regulation of multiple genes. The current study focuses on the role of p53 signaling in RVFV infection and viral replication. These results show an up-regulation of p53 phosphorylation at several serine sites after RVFV MP-12 infection that is highly dependent on the viral protein NSs. qRT-PCR data showed a transcriptional up-regulation of several p53 targeted genes involved in cell cycle and apoptosis regulation following RVFV infection. Cell viability assays demonstrate that loss of p53 results in less RVFV induced cell death. Furthermore, decreased viral titers in p53 null cells indicate that RVFV utilizes p53 to enhance viral production. Collectively, these experiments indicate that the p53 signaling pathway is utilized during RVFV infection to induce cell death and increase viral production.

Links

PubMed PMC3344861 Online version:10.1371/journal.pone.0036327

Keywords

Active Transport, Cell Nucleus; Apoptosis; Cell Line; Cell Nucleus/metabolism; Humans; Phosphorylation; Rift Valley fever virus/physiology; Signal Transduction; Transcription, Genetic; Tumor Suppressor Protein p53/chemistry; Tumor Suppressor Protein p53/deficiency; Tumor Suppressor Protein p53/genetics; Tumor Suppressor Protein p53/metabolism; Up-Regulation; Viral Nonstructural Proteins/metabolism; Virus Replication

Significance

Annotations

Gene product Qualifier GO Term Evidence Code with/from Aspect Extension Notes Status

HUMAN:P53

GO:0016032: viral reproduction

ECO:0000315:

P

Figure 7

complete
CACAO 6713

HUMAN:P53

involved_in

GO:0016032: viral process

ECO:0000315: mutant phenotype evidence used in manual assertion

P

Seeded From UniProt

complete


See also

References

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