Skip to main content

Advertisement

Log in

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

  • Research Article
  • Published:
Cellular and Molecular Life Sciences CMLS Aims and scope Submit manuscript

Abstract

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.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to C. Kruse.

Additional information

Received 20 June 2003; received after revision 25 July 2003; accepted 29 July 2003

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kruse, C., Willkomm, D., Gebken, J. et al. The multi-KH protein vigilin associates with free and membrane-bound ribosomes. CMLS, Cell. Mol. Life Sci. 60, 2219–2227 (2003). https://doi.org/10.1007/s00018-003-3235-0

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00018-003-3235-0

Navigation