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The RNA-binding protein HuR (Elavl1) is essential for the B cell antibody response

Post-transcriptional regulation of mRNA by the RNA binding protein HuR (Elavl1) is required in B cells for the germinal centre reaction and for the production of class-switched antibodies in response to T-independent antigens. Transcriptome-wide examination of RNA isoforms, abundance and translation...

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Detalles Bibliográficos
Autores principales: Diaz-Muñoz, Manuel D., Bell, Sarah E., Fairfax, Kirsten, Monzon-Casanova, Elisa, Cunningham, Adam F., Gonzalez-Porta, Mar, Andrews, Simon R., Bunik, Victoria I., Zarnack, Kathi, Curk, Tomaž, Heggermont, Ward A., Heymans, Stephane, Gibson, Gary E., Kontoyiannis, Dimitris L., Ule, Jernej, Turner, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4479220/
https://www.ncbi.nlm.nih.gov/pubmed/25706746
http://dx.doi.org/10.1038/ni.3115
Descripción
Sumario:Post-transcriptional regulation of mRNA by the RNA binding protein HuR (Elavl1) is required in B cells for the germinal centre reaction and for the production of class-switched antibodies in response to T-independent antigens. Transcriptome-wide examination of RNA isoforms, abundance and translation in HuR-deficient B cells, together with direct measurements of HuR-RNA interaction, revealed that HuR-dependent mRNA splicing affects hundreds of transcripts including the dihydrolipoamide S-succinyltransferase (Dlst), a subunit of the 2-oxoglutarate dehydrogenase complex (αKGDH). In the absence of HuR, defective mitochondrial metabolism results in high amounts of reactive oxygen species and B cell death. Our study shows how post-transcriptional processes control the balance of energy metabolism required for B cell proliferation and differentiation.