Artículos de revistas
Musashi mediates translational repression of the Drosophila hypoxia inducible factor.
Fecha
2016-05Registro en:
Bertolin, Agustina Paola; Katz, Maximiliano Javier; Yano, Masato; Pozzi, María Berta; Acevedo, Julieta María; et al.; Musashi mediates translational repression of the Drosophila hypoxia inducible factor.; Oxford University Press; Nucleic Acids Research; 44; 16; 5-2016; 7555-7567
0305-1048
1362-4962
CONICET Digital
CONICET
Autor
Bertolin, Agustina Paola
Katz, Maximiliano Javier
Yano, Masato
Pozzi, María Berta
Acevedo, Julieta María
Blanco Obregón, Dalmiro Manuel
Gándara, Lautaro
Sorianello, Eleonora Mariana
Kanda, Hiroshi
Okano, Hideyuki
Srebrow, Anabella
Wappner, Pablo
Resumen
Adaptation to hypoxia depends on a conserved α/β heterodimeric transcription factor called Hypoxia Inducible Factor (HIF), whose α-subunit is regulated by oxygen through different concurrent mechanisms. In this study, we have identified the RNA binding protein dMusashi, as a negative regulator of the fly HIF homologue Sima. Genetic interaction assays suggested that dMusashi participates of the HIF pathway, and molecular studies carried out in Drosophila cell cultures showed that dMusashi recognizes a Musashi Binding Element in the 3' UTR of the HIFα transcript, thereby mediating its translational repression in normoxia. In hypoxic conditions dMusashi is downregulated, lifting HIFα repression and contributing to trigger HIF-dependent gene expression. Analysis performed in mouse brains revealed that murine Msi1 protein physically interacts with HIF-1α transcript, suggesting that the regulation of HIF by Msi might be conserved in mammalian systems. Thus, Musashi is a novel regulator of HIF that inhibits responses to hypoxia specifically when oxygen is available.