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The tumour suppressor APC promotes HIV-1 assembly via interaction with Gag precursor protein

Diverse cellular proteins and RNAs are tightly regulated in their subcellular localization to exert their local function. Here we report that the tumour suppressor adenomatous polyposis coli protein (APC) directs the localization and assembly of human immunodeficiency virus (HIV)-1 Gag polyprotein a...

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Detalles Bibliográficos
Autores principales: Miyakawa, Kei, Nishi, Mayuko, Matsunaga, Satoko, Okayama, Akiko, Anraku, Masaki, Kudoh, Ayumi, Hirano, Hisashi, Kimura, Hirokazu, Morikawa, Yuko, Yamamoto, Naoki, Ono, Akira, Ryo, Akihide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5290283/
https://www.ncbi.nlm.nih.gov/pubmed/28134256
http://dx.doi.org/10.1038/ncomms14259
Descripción
Sumario:Diverse cellular proteins and RNAs are tightly regulated in their subcellular localization to exert their local function. Here we report that the tumour suppressor adenomatous polyposis coli protein (APC) directs the localization and assembly of human immunodeficiency virus (HIV)-1 Gag polyprotein at distinct membrane components to enable the efficient production and spread of infectious viral particles. A proteomic analysis and subsequent biomolecular interaction assay reveals that the carboxyl terminus of APC interacts with the matrix region of Gag. Ectopic expression of APC, but not its familial adenomatous polyposis-related truncation mutant, prominently enhances HIV-1 production. Conversely, the depletion of APC leads to a significant decrease in membrane targeting of viral components, resulting in the severe loss of production of infectious virions. Furthermore, APC promotes the directional assembly of viral components at virological synapses, thereby facilitating cell-to-cell viral transmission. These findings reveal an unexpected role of APC in the directional spread of HIV-1.