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RETRACTED: Identification of programmed translational-1 frameshifting sites in the genome of Saccharomyces cerevisiae (Retracted Article. See vol 16, pg 1074, 2006)
被引:5
|作者:
Bekaert, M
Richard, H
Prum, B
Rousset, JP
[1
]
机构:
[1] Univ Paris 11, CNRS, UMR 8621, Inst Genet & Microbiol, F-91405 Orsay, France
[2] Univ Evry, INRA, CNRS, Lab Stat & Genome, F-91000 Evry, France
关键词:
D O I:
10.1101/gr.4258005
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Frameshifting is a recoding event that allows the expression of two polypeptides from the same mRNA molecule. Most recoding events described so far are used by viruses and transposons to express their replicase protein. The very few number of cellular proteins known to be expressed by a -1 ribosomal frameshifting has been identified by chance. The goal of the present work was to set Lip a systematic strategy, based oil complementary bioinformatics, molecular biology, and functional approaches, Without a priori knowledge of the mechanism involved. Two independent methods were devised. The first looks for genomic regions in which two ORFs, each carrying a protein pattern, are in a frameshifted arrangement. The second uses Hidden Markov Models and likelihood in a two-step approach. When this strategy was applied to the Saccharomyces cerevisiae genome, 189 candidate regions were found, of which 58 were further functionally investigated. Twenty-eight of them expressed a full-length mRNA covering the two ORFs, and II showed a -1 frameshift efficiency varying from 5% to 13% (50-fold higher than background), some of which corresponds to genes with known functions. From other ascomycetes, four frameshifted ORFs are found fully conserved. Strikingly, most of the candidates do not display a classical viral-like frameshift signal and would have escaped a search based oil current models of frameshifting. These results strongly suggest that -1 frameshifting might be more widely distributed than previously thought.
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页码:1411 / 1420
页数:10
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