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Reduced stability of mRNA secondary structure near the translation-initiation site in dsDNA viruses

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Title: Reduced stability of mRNA secondary structure near the translation-initiation site in dsDNA viruses
Author(s): Zhou, Tong; Wilke, Claus O.
Subject(s): viruses stability
Abstract: Background Recent studies have demonstrated a selection pressure for reduced mRNA secondary-structure stability near the start codon of coding sequences. This selection pressure can be observed in bacteria, archaea, and eukaryotes, and is likely caused by the requirement of efficient translation initiation in cellular organism. Results Here, we surveyed the complete genomes of 650 dsDNA virus strains for signals of reduced stability of mRNA secondary structure near the start codon. Our analysis included viruses infecting eukaryotic, prokaryotic, and archaeic hosts. We found that many viruses showed evidence for reduced mRNA secondary-structure stability near the start codon. The effect was most pronounced in viruses infecting prokaryotes, but was also observed in viruses infecting eukaryotes and archaea. The reduction in stability generally increased with increasing genomic GC content. For bacteriophage, the reduction was correlated with a corresponding reduction of stability in the phage hosts. Conclusions We conclude that reduced stability of the mRNA secondary structure near the start codon is a common feature for dsDNA viruses, likely driven by the same selective pressures that cause it in cellular organisms.
Issue Date: 2011-03-07
Publisher: BioMed Central
Citation Info: Zhou, T. & Wilke, C. O. 2011. Reduced stability of mRNA secondary structure near the translation-initiation site in dsDNA viruses. Bmc Evolutionary Biology, 11. DOI: 10.1186/1471-2148-11-59
Type: Article
Description: © 2011 Zhou and Wilke; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. DOI: 10.1186/1471-2148-11-59
URI: http://hdl.handle.net/10027/7731
ISSN: 1471-2148
Sponsor: This work was supported by NIH grant R01 GM088344.
Date Available in INDIGO: 2011-05-27
 

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