Number of the records: 1  

Human eIF3b and eIF3a serve as the nucleation core for the assembly of eIF3 into two interconnected modules: the yeast-like core and the octamer

  1. 1.
    0468862 - MBÚ 2017 RIV GB eng J - Journal Article
    Wagner, Susan - Herrmannová, Anna - Šikrová, Darina - Valášek, Leoš Shivaya
    Human eIF3b and eIF3a serve as the nucleation core for the assembly of eIF3 into two interconnected modules: the yeast-like core and the octamer.
    Nucleic Acids Research. Roč. 44, č. 22 (2016), s. 10772-10788. ISSN 0305-1048. E-ISSN 1362-4962
    R&D Projects: GA ČR(CZ) GA14-05394S
    EU Projects: Wellcome Trust(GB) 090812/B/09/A
    Institutional support: RVO:61388971
    Keywords : Human eIF3b * nucleation core * yeast-like core
    Subject RIV: EE - Microbiology, Virology
    Impact factor: 10.162, year: 2016

    The 12-subunit mammalian eIF3 is the largest and most complex translation initiation factor and has been implicated in numerous steps of translation initiation, termination and ribosomal recycling. Imbalanced eIF3 expression levels are observed in various types of cancer and developmental disorders, but the consequences of altered eIF3 subunit expression on its overall structure and composition, and on translation in general, remain unclear. We present the first complete in vivo study monitoring the effects of RNAi knockdown of each subunit of human eIF3 on its function, subunit balance and integrity. We show that the eIF3b and octameric eIF3a subunits serve as the nucleation core around which other subunits assemble in an ordered way into two interconnected modules: the yeast-like core and the octamer, respectively. In the absence of eIF3b neither module forms in vivo, whereas eIF3d knock-down results in severe proliferation defects with no impact on eIF3 integrity. Disrupting the octamer produces an array of subcomplexes with potential roles in translational regulation. This study, outlining the mechanism of eIF3 assembly and illustrating how imbalanced expression of eIF3 subunits impacts the factor's overall expression profile, thus provides a comprehensive guide to the human eIF3 complex and to the relationship between eIF3 misregulation and cancer.
    Permanent Link: http://hdl.handle.net/11104/0267384

     
    FileDownloadSizeCommentaryVersionAccess
    128_Human eIF3b and eIF3a serve as.pdf67.7 MBPublisher’s postprintrequire
     
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.