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RNA helicase EIF4A1-mediated translation is essential for the GC response

Title: RNA helicase EIF4A1-mediated translation is essential for the GC response
Authors: Screen, Michael; Matheson, Louise S.; Howden, Andrew J. M.; Strathdee, Douglas; Willis, Anne E.; Bushell, Martin; Sansom, Owen; Turner, Martin
Source: Screen, M, Matheson, L S, Howden, A J M, Strathdee, D, Willis, A E, Bushell, M, Sansom, O & Turner, M 2024, 'RNA helicase EIF4A1-mediated translation is essential for the GC response', Life Science Alliance, vol. 7, no. 2, e202302301. https://doi.org/10.26508/lsa.202302301
Publication Year: 2024
Collection: Discovery - University of Dundee Online Publications
Subject Terms: Animals; Mice; Eukaryotic Initiation Factor-4A/genetics; RNA Helicases/metabolism; B-Lymphocytes; /dk/atira/pure/subjectarea/asjc/1300/1301; name=Biochemistry; Genetics and Molecular Biology (miscellaneous); /dk/atira/pure/subjectarea/asjc/2300/2307; name=Health; Toxicology and Mutagenesis; /dk/atira/pure/subjectarea/asjc/1100/1110; name=Plant Science; /dk/atira/pure/subjectarea/asjc/2300/2303; name=Ecology
Description: EIF4A1 and cofactors EIF4B and EIF4H have been well characterised in cancers, including B cell malignancies, for their ability to promote the translation of oncogenes with structured 5' untranslated regions. However, very little is known of their roles in nonmalignant cells. Using mouse models to delete Eif4a1, Eif4b or Eif4h in B cells, we show that EIF4A1, but not EIF4B or EIF4H, is essential for B cell development and the germinal centre response. After B cell activation in vitro, EIF4A1 facilitates an increased rate of protein synthesis, MYC expression, and expression of cell cycle regulators. However, EIF4A1-deficient cells remain viable, whereas inhibition of EIF4A1 and EIF4A2 by Hippuristanol treatment induces cell death.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: English
ISSN: 2575-1077
Relation: info:eu-repo/semantics/altIdentifier/pmid/38011999; info:eu-repo/semantics/altIdentifier/pissn/2575-1077
DOI: 10.26508/lsa.202302301
Availability: https://discovery.dundee.ac.uk/en/publications/1085ccc6-a82e-49ff-8af7-a5aecd02d59b; https://doi.org/10.26508/lsa.202302301; https://discovery.dundee.ac.uk/ws/files/114288963/e202302301.full.pdf
Rights: info:eu-repo/semantics/openAccess ; http://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.56E8FD1E
Database: BASE