Functional equivalence of translation factor eIF5B from Candida albicans and Saccharomyces cerevisiae

Eukaryotic translation initiation factor 513 (eIF5B) plays a role in recognition of the AUG codon in conjunction with translation factor eIF2, and promotes joining of the 60S ribosomal subunit. To see whether the eIF5B proteins of other organisms function in Saccharomyces cerevisiae, we cloned the c...

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Veröffentlicht in:Molecules and cells 2008, 25(2), , pp.172-177
Hauptverfasser: Jun, K.O. (Sunchon National University, Sunchon, Republic of Korea), Yang, E.J. (Sunchon National University, Sunchon, Republic of Korea), Lee, B.J. (Sunchon National University, Sunchon, Republic of Korea), Park, J.R. (Sunchon National University, Sunchon, Republic of Korea), Lee, J.H. (Konyang University College of Medicine, Nonsan, Republic of Korea), Choi, S.K. (Sunchon National University, Sunchon, Republic of Korea), E-mail: sangkic@sunchon.ac.kr
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Sprache:eng
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Zusammenfassung:Eukaryotic translation initiation factor 513 (eIF5B) plays a role in recognition of the AUG codon in conjunction with translation factor eIF2, and promotes joining of the 60S ribosomal subunit. To see whether the eIF5B proteins of other organisms function in Saccharomyces cerevisiae, we cloned the corresponding genes from Oryza sativa, Arabidopsis thaliana, Aspergillus nidulans and Candida albican and expressed them under the control of the galactose-inducible GAL promoter in the fun12Δ strain of Saccharomyces cerevisiae. Expression of Candida albicans eIF5B complemented the slow-growth phenotype of the fun12Δ strain, but that of Aspergillus nidulance did not, despite the fact that its protein was expressed better than that of Candida albicans. The Arabidopsis thaliana protein was also not functional in Saccharomyces. These results reveal that the eIF5B in Candida albicans has a close functional relationship with that of Sacharomyces cerevisiae, as also shown by a phylogenetic analysis based on the amino acid sequences of the eIF5Bs.
ISSN:1016-8478
0219-1032
DOI:10.1016/S1016-8478(23)17567-4