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Ambiguous decoding of the CUG codon alters the functionality of the Candida albicans translation initiation factor 4E
Z. Feketová, T. Masek, V. Vopálenský, M. Pospísek,
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
ProQuest Central
from 2003-03-01 to 1 year ago
Medline Complete (EBSCOhost)
from 2006-01-01 to 2014-12-31
Health & Medicine (ProQuest)
from 2003-03-01 to 1 year ago
Wiley Online Library (archiv)
from 2001-01-01 to 2012-12-31
Oxford Journals Open Access Collection
from 2001-04-01
- MeSH
- Candida albicans genetics growth & development metabolism radiation effects MeSH
- Genes, Essential MeSH
- Eukaryotic Initiation Factor-4E metabolism MeSH
- Fungal Proteins metabolism MeSH
- Genes, Fungal MeSH
- Codon MeSH
- Models, Molecular MeSH
- Molecular Sequence Data MeSH
- Protein Biosynthesis MeSH
- Amino Acid Sequence MeSH
- Sequence Homology MeSH
- Sequence Alignment MeSH
- Amino Acid Substitution genetics MeSH
- Temperature MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
The eukaryotic translation initiation factor 4E is an essential and highly conserved protein. As a part of the translational machinery, it plays a key role in the recruitment of mRNA via binding to its m(7)GpppN 5' terminal cap structure. The opportunistic human pathogen Candida albicans is the only known eukaryotic organism with the ability to survive defects in mRNA capping, which suggests unique features of its eIF4E protein. Here, we provide the first experimental evidence of the function of the C. albicans putative gene orf19.7626 as an eIF4E protein. We also show that Ca4E(Leu116) and Ca4E(Ser116) protein variants, both of which occur naturally in C. albicans due to the ambiguous decoding of the CUG(116) codon, display different sensitivities to elevated temperature. Our results clearly point to the importance of the S4-H4 loop for the function of the Ca4E translation initiation factor, and suggest the possible regulatory role of the codon-reading ambiguity within this loop in C. albicans. We proved Saccharomyces cerevisiae as a useful tool organism for studies of C. albicans translation initiation apparatus.
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