The multi-KH protein vigilin associates with free and membrane-bound ribosomes

C. Kruse*, D. Willkomm, J. Gebken, A. Schuh, H. Stossberg, T. Vollbrandt, P. K. Müller

*Corresponding author for this work
14 Citations (Scopus)


The-multi-KH domain protein vigilin has been identified by ex vivo experiments as both a tRNA-and/or mRNA-binding protein. We show here that in vitro under conditions previously shown to allow tRNA binding, recombinant vigilin also binds to selected mRNA species and ribosomal RNA. An in vivo link of vigilin to mRNA and rRNA was elucidated by several approaches. (i) Coexpression/costimulation of vigilin was found with many other proteins independently of whether their mRNA was translated on free or membrane-bound ribosomes. (ii) A close codistribution of vigilin with free ribosomes was seen in the cytoplasm while nucleoli were a major organelle of vigilin accumulation in the nucleus. (iii) Furthermore, free and membrane-bound ribosomes can be enriched for vigilin which suggests that this binding does not depend on the class of mRNA translated. Therefore, we suggest that vigilin does not distinguish between free or membrane-bound ribosomes but is generally necessary for the localization of mRNAs to actively translating ribosomes.

Original languageEnglish
JournalCellular and Molecular Life Sciences
Issue number10
Pages (from-to)2219-2227
Number of pages9
Publication statusPublished - 01.10.2003

Research Areas and Centers

  • Academic Focus: Center for Infection and Inflammation Research (ZIEL)


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