Display Settings:

Format

Send to:

Choose Destination
    Cell. 2007 Oct 19;131(2):286-99.

    Recycling of eukaryotic posttermination ribosomal complexes.

    Source

    Department of Microbiology and Immunology, SUNY Downstate Medical Center, Brooklyn, NY 11203, USA.

    Abstract

    After translational termination, mRNA and P site deacylated tRNA remain associated with ribosomes in posttermination complexes (post-TCs), which must therefore be recycled by releasing mRNA and deacylated tRNA and by dissociating ribosomes into subunits. Recycling of bacterial post-TCs requires elongation factor EF-G and a ribosome recycling factor RRF. Eukaryotes do not encode a RRF homolog, and their mechanism of ribosomal recycling is unknown. We investigated eukaryotic recycling using post-TCs assembled on a model mRNA encoding a tetrapeptide followed by a UAA stop codon and report that initiation factors eIF3, eIF1, eIF1A, and eIF3j, a loosely associated subunit of eIF3, can promote recycling of eukaryotic post-TCs. eIF3 is the principal factor that promotes splitting of posttermination ribosomes into 60S subunits and tRNA- and mRNA-bound 40S subunits. Its activity is enhanced by eIFs 3j, 1, and 1A. eIF1 also mediates release of P site tRNA, whereas eIF3j ensures subsequent dissociation of mRNA.

    PMID:
    17956730
    [PubMed - indexed for MEDLINE]
    PMCID: PMC2651563
    Free PMC Article

    Images from this publication.See all images (7) Free text

    Figure 7
    Figure 4
    Figure 2
    Figure 5
    Figure 3
    Figure 1
    Figure 6

      Supplemental Content

      Click here to read Click here to read

      Recent activity

      Your browsing activity is empty.

      Activity recording is turned off.

      Turn recording back on

      See more...
      Write to the Help Desk