Murine leukemia virus (MLV) P50 protein induces cell transformation via transcriptional regulatory function
BELKHIR, Khalid
Université de Montpellier [UM]
Institut des Sciences de l'Evolution de Montpellier [UMR ISEM]
Université de Montpellier [UM]
Institut des Sciences de l'Evolution de Montpellier [UMR ISEM]
GODEFROY, Nelly
Université de Montpellier [UM]
Institut des Sciences de l'Evolution de Montpellier [UMR ISEM]
Université de Montpellier [UM]
Institut des Sciences de l'Evolution de Montpellier [UMR ISEM]
MOUGEL, Marylene
Université de Montpellier [UM]
Institut de Recherche en Infectiologie de Montpellier [IRIM]
< Réduire
Université de Montpellier [UM]
Institut de Recherche en Infectiologie de Montpellier [IRIM]
Langue
EN
Article de revue
Ce document a été publié dans
Retrovirology. 2023-09-12, vol. 20, n° 1, p. 16
Résumé en anglais
Background The murine leukemia virus (MLV) has been a powerful model of pathogenesis for the discovery of genes involved in cancer. Its splice donor (SD')-associated retroelement (SDARE) is important for infectivity and ...Lire la suite >
Background The murine leukemia virus (MLV) has been a powerful model of pathogenesis for the discovery of genes involved in cancer. Its splice donor (SD')-associated retroelement (SDARE) is important for infectivity and tumorigenesis, but the mechanism remains poorly characterized. Here, we show for the first time that P50 protein, which is produced from SDARE, acts as an accessory protein that transregulates transcription and induces cell transformation. Results By infecting cells with MLV particles containing SDARE transcript alone (lacking genomic RNA), we show that SDARE can spread to neighbouring cells as shown by the presence of P50 in infected cells. Furthermore, a role for P50 in cell transformation was demonstrated by CCK8, TUNEL and anchorage-independent growth assays. We identified the integrase domain of P50 as being responsible for transregulation of the MLV promoter using luciferase assay and RTqPCR with P50 deleted mutants. Transcriptomic analysis furthermore revealed that the expression of hundreds of cellular RNAs involved in cancerogenesis were deregulated in the presence of P50, suggesting that P50 induces carcinogenic processes via its transcriptional regulatory function. Conclusion We propose a novel SDARE-mediated mode of propagation of the P50 accessory protein in surrounding cells. Moreover, due to its transforming properties, P50 expression could lead to a cellular and tissue microenvironment that is conducive to cancer development.< Réduire
Mots clés en anglais
Retrovirus
Murine leukemia virus
SD'
P50
Cancerogenesis
Leukemia
Transcription regulation
Transcriptomic
Unités de recherche