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Molecular and Cellular Biology, May 2002, p. 3301-3315, Vol. 22, No. 10
0270-7306/02/$04.00+0     DOI: 10.1128/MCB.22.10.3301-3315.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Poly(A)-Binding Protein Acts in Translation Termination via Eukaryotic Release Factor 3 Interaction and Does Not Influence [PSI+] Propagation

Bertrand Cosson,1 Anne Couturier,1 Svetlana Chabelskaya,2 Denis Kiktev,2 Sergey Inge-Vechtomov,2 Michel Philippe,1* and Galina Zhouravleva1,2

Universite de Rennes 1, CNRS UMR 6061, 35043 Rennes Cedex, France,1 Department of Genetics, St. Petersburg State University, 199034 St. Petersburg, Russia2

Received 11 July 2001/ Returned for modification 18 September 2001/ Accepted 20 February 2002

Recent studies of translational control suggest that translation termination may not be simply the end of synthesizing a protein but rather be involved in modulating both the translation efficiency and stability of a given transcript. Using recombinant eukaryotic release factor 3 (eRF3) and cellular extracts, we have shown for Saccharomyces cerevisiae that yeast eRF3 and Pab1p can interact. This interaction, mediated by the N+M domain of eRF3 and amino acids 473 to 577 of Pab1p, was demonstrated to be direct by the two-hybrid approach. We confirmed that a genetic interaction exists between eRF3 and Pab1p and showed that Pab1p overexpression enhances the efficiency of termination in SUP35 (eRF3) mutant and [PSI+] cells. This effect requires the interaction of Pab1p with eRF3. These data further strengthen the possibility that Pab1p has a role in coupling translation termination events with initiation of translation. Several lines of evidence indicate that Pab1p does not influence [PSI+] propagation. First, "[PSI+]-no-more" mutations do not affect eRF3-Pab1p two-hybrid interaction. Second, overexpression of PAB1 does not cure the [PSI+] phenotype or solubilize detectable amounts of eRF3. Third, prion-curing properties of overexpressed HSP104p, which is required for formation and maintenance of [PSI+], were not modified by excess Pab1p.

* Corresponding author. Mailing address: Universite de Rennes 1, CNRS UMR 6061, 2 av. Pr. Léon Bernard, 35043 Rennes Cedex, France. Phone: 33 (0) 2 23 23 44 70. Fax: 33 (0) 2 23 23 44 78. E-mail: michel.philippe{at}univ-rennes1.fr.

Molecular and Cellular Biology, May 2002, p. 3301-3315, Vol. 22, No. 10
0022-538X/02/$04.00+0     DOI: 10.1128/MCB.22.10.3301-3315.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.



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