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Evidence for core exosome independent function of the nuclear exoribonuclease Rrp6p.

Nucleic acids research | Dec 28, 2008

The RNA exosome processes and degrades RNAs in archaeal and eukaryotic cells. Exosomes from yeast and humans contain two active exoribonuclease components, Rrp6p and Dis3p/Rrp44p. Rrp6p is concentrated in the nucleus and the dependence of its function on the nine-subunit core exosome and Dis3p remains unclear. We found that cells lacking Rrp6p accumulate poly(A)+ rRNA degradation intermediates distinct from those found in cells depleted of Dis3p, or the core exosome component Rrp43p. Depletion of Dis3p in the absence of Rrp6p causes a synergistic increase in the levels of degradation substrates common to the core exosome and Rrp6p, but has no effect on Rrp6p-specific substrates. Rrp6p lacking a portion of its C-terminal domain no longer co-purifies with the core exosome, but continues to carry out RNA 3'-end processing of 5.8S rRNA and snoRNAs, as well as the degradation of certain truncated Rrp6-specific rRNA intermediates. However, disruption of Rrp6p-core exosome interaction results in the inability of the cell to efficiently degrade certain poly(A)+ rRNA processing products that require the combined activities of Dis3p and Rrp6p. These findings indicate that Rrp6p may carry out some of its critical functions without physical association with the core exosome.

Pubmed ID: 18940861 RIS Download

Mesh terms: Cell Nucleus | Exoribonucleases | Exosome Multienzyme Ribonuclease Complex | Gene Deletion | Nuclear Proteins | Protein Structure, Tertiary | Protein Subunits | RNA 3' End Processing | RNA, Ribosomal | Saccharomyces cerevisiae Proteins | Sequence Deletion

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Associated grants

  • Agency: NIGMS NIH HHS, Id: R01 GM059898

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