Base Composition and Translational Selection are Insufficient to Explain Codon Usage Bias in Plant Viruses

被引:30
作者
Cardinale, Daniel J. [1 ]
DeRosa, Kate [1 ]
Duffy, Siobain [1 ]
机构
[1] Rutgers State Univ, Sch Environm & Biol Sci, Dept Ecol Evolut & Nat Resources, New Brunswick, NJ 08901 USA
来源
VIRUSES-BASEL | 2013年 / 5卷 / 01期
关键词
synonymous codon usage; translational selection; genomic content; mutational bias; SINGLE-STRANDED-DNA; ESCHERICHIA-COLI; RAMAN-SPECTROSCOPY; MOLECULAR CHARACTERIZATION; PHYLOGENETIC EVIDENCE; RESPECTIVE CODONS; GENE-EXPRESSION; PROTEIN GENES; TRANSFER-RNAS; RATES;
D O I
10.3390/v5010162
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Viral codon usage bias may be the product of a number of synergistic or antagonistic factors, including genomic nucleotide composition, translational selection, genomic architecture, and mutational or repair biases. Most studies of viral codon bias evaluate only the relative importance of genomic base composition and translational selection, ignoring other possible factors. We analyzed the codon preferences of ssRNA (luteoviruses and potyviruses) and ssDNA (geminiviruses) plant viruses that infect translationally distinct monocot and dicot hosts. We found that neither genomic base composition nor translational selection satisfactorily explains their codon usage biases. Furthermore, we observed a strong relationship between the codon preferences of viruses in the same family or genus, regardless of host or genomic nucleotide content. Our results suggest that analyzing codon bias as either due to base composition or translational selection is a false dichotomy that obscures the role of other factors. Constraints such as genomic architecture and secondary structure can and do influence codon usage in plant viruses, and likely in viruses of other hosts.
引用
收藏
页码:162 / 181
页数:20
相关论文
共 66 条
[1]   Codon usage bias amongst plant viruses [J].
Adams, MJ ;
Antoniw, JF .
ARCHIVES OF VIROLOGY, 2004, 149 (01) :113-135
[2]  
Andret-Link P, 2005, J PLANT PATHOL, V87, P153
[3]   DIVERSITY IN G+C CONTENT AT THE 3RD POSITION OF CODONS IN VERTEBRATE GENES AND ITS CAUSE [J].
AOTA, S ;
IKEMURA, T .
NUCLEIC ACIDS RESEARCH, 1986, 14 (16) :6345-6355
[4]  
AU KG, 1992, J BIOL CHEM, V267, P12142
[5]   Codon usage domains over bacterial chromosomes [J].
Bailly-Bechet, Marc ;
Danchin, Antoine ;
Iqbal, Mudassar ;
Marsili, Matteo ;
Vergassola, Massimo .
PLOS COMPUTATIONAL BIOLOGY, 2006, 2 (04) :263-275
[6]   DIFFERENCES IN SECONDARY STRUCTURE BETWEEN PACKAGED AND UNPACKAGED SINGLE-STRANDED-DNA OF BACTERIOPHAGE PHI-X174 DETERMINED BY RAMAN-SPECTROSCOPY - A MODEL FOR PHI-X174 DNA PACKAGING [J].
BENEVIDES, JM ;
STOW, PL ;
ILAG, LL ;
INCARDONA, NL ;
THOMAS, GJ .
BIOCHEMISTRY, 1991, 30 (20) :4855-4863
[7]  
BENNETZEN JL, 1982, J BIOL CHEM, V257, P3026
[8]   Cytidine deamination of retroviral DNA by diverse APOBEC proteins [J].
Bishop, KN ;
Holmes, RK ;
Sheehy, AM ;
Davidson, NO ;
Cho, SJ ;
Malim, MH .
CURRENT BIOLOGY, 2004, 14 (15) :1392-1396
[9]   Slow Fitness Recovery in a Codon-Modified Viral Genome [J].
Bull, J. J. ;
Molineux, I. J. ;
Wilke, C. O. .
MOLECULAR BIOLOGY AND EVOLUTION, 2012, 29 (10) :2997-3004
[10]   Characterization of Synonymous Codon Usage Bias in the Duck Plague Virus UL35 Gene [J].
Cai, Ming-Sheng ;
Cheng, An-Chun ;
Wang, Ming-Shu ;
Zhao, Li-Chan ;
Zhu, De-Kang ;
Luo, Qi-Hui ;
Liu, Fei ;
Chen, Xiao-Yue .
INTERVIROLOGY, 2009, 52 (05) :266-278