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Zika virus disrupts molecular fingerprinting of human neurospheres

Zika virus (ZIKV) has been associated with microcephaly and other brain abnormalities; however, the molecular consequences of ZIKV to human brain development are still not fully understood. Here we describe alterations in human neurospheres derived from induced pluripotent stem (iPS) cells infected...

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Detalles Bibliográficos
Autores principales: Garcez, Patricia P., Nascimento, Juliana Minardi, de Vasconcelos, Janaina Mota, Madeiro da Costa, Rodrigo, Delvecchio, Rodrigo, Trindade, Pablo, Loiola, Erick Correia, Higa, Luiza M., Cassoli, Juliana S., Vitória, Gabriela, Sequeira, Patricia C., Sochacki, Jaroslaw, Aguiar, Renato S., Fuzii, Hellen Thais, de Filippis, Ana M. Bispo, da Silva Gonçalves Vianez Júnior, João Lídio, Tanuri, Amilcar, Martins-de-Souza, Daniel, Rehen, Stevens K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5256095/
https://www.ncbi.nlm.nih.gov/pubmed/28112162
http://dx.doi.org/10.1038/srep40780
Descripción
Sumario:Zika virus (ZIKV) has been associated with microcephaly and other brain abnormalities; however, the molecular consequences of ZIKV to human brain development are still not fully understood. Here we describe alterations in human neurospheres derived from induced pluripotent stem (iPS) cells infected with the strain of Zika virus that is circulating in Brazil. Combining proteomics and mRNA transcriptional profiling, over 500 proteins and genes associated with the Brazilian ZIKV infection were found to be differentially expressed. These genes and proteins provide an interactome map, which indicates that ZIKV controls the expression of RNA processing bodies, miRNA biogenesis and splicing factors required for self-replication. It also suggests that impairments in the molecular pathways underpinning cell cycle and neuronal differentiation are caused by ZIKV. These results point to biological mechanisms implicated in brain malformations, which are important to further the understanding of ZIKV infection and can be exploited as therapeutic potential targets to mitigate it.