Predicting evolution from genomics: experimental evolution of bacteriophage T7

被引:45
作者
Bull, J. J. [1 ]
Molineux, I. J. [1 ]
机构
[1] Univ Texas Austin, Inst Mol & Cellular Biol, Austin, TX 78712 USA
关键词
experimental evolution; bacteriophage; genomics; sequence; adaptation;
D O I
10.1038/sj.hdy.6801087
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
A wealth of molecular biology has been exploited in designing and interpreting experimental evolution studies with bacteriophage T7. The modest size of its genome (40 kb dsDNA) and the ease of making genetic constructs, combined with the many genetic resources for its host (Escherichia coli), have enabled comprehensive and detailed studies of experimental adaptations. In several studies, the genome was specifically altered (gene knockouts, gene replacements, reordering of genetic elements) such that a priori knowledge of genetics and biochemistry of the phage could be used to predict the pathways of compensatory evolution when the modified phage is adapted to recover fitness. In other work, the phage has been adapted to specific environmental conditions chosen to select phenotypic outcomes with a quantitative basis, and the molecular bases of that evolution have been explored. Predicting the outcomes of these adaptations has been challenging. In hindsight, one-third to one-half of the compensatory nucleotide changes observed during the adaptation can be rationalized based on T7 biology. This rationalization usually only applies at the genetic level - a gene product may be known to be involved in the affected pathway, but it usually remains unknown how the observed change affects activity. The progress is encouraging, but the prediction of experimental evolution pathways remains far from complete, and is still sometimes confounded by observation when an adaptation yields a completely unexpected outcome.
引用
收藏
页码:453 / 463
页数:11
相关论文
共 58 条
[1]   Rapid evolution of diminished transformability in Acinetobacter baylyi [J].
Bacher, Jamie M. ;
Metzgar, David ;
de Crecy-Lagard, Valrie .
JOURNAL OF BACTERIOLOGY, 2006, 188 (24) :8534-8542
[2]   Compensatory evolution in response to a novel RNA polymerase: Orthologous replacement of a central network gene [J].
Bull, J. J. ;
Springman, R. ;
Molineux, I. J. .
MOLECULAR BIOLOGY AND EVOLUTION, 2007, 24 (04) :900-908
[3]   Optimality models of phage life history and parallels in disease evolution [J].
Bull, J. J. .
JOURNAL OF THEORETICAL BIOLOGY, 2006, 241 (04) :928-938
[4]   A general mechanism for viral resistance to suicide gene expression [J].
Bull, JJ ;
Badgett, MR ;
Molineux, IJ .
JOURNAL OF MOLECULAR EVOLUTION, 2001, 53 (01) :47-54
[5]   Evolvability of an RNA virus is determined by its mutational neighbourhood [J].
Burch, CL ;
Chao, L .
NATURE, 2000, 406 (6796) :625-628
[6]  
Chao L, 1997, GENETICS, V147, P953
[7]   Recombination speeds adaptation by reducing competition between beneficial mutations in populations of Escherichia coli [J].
Cooper, Tim F. .
PLOS BIOLOGY, 2007, 5 (09) :1899-1905
[8]   FITNESS AS A FUNCTION OF BETA-GALACTOSIDASE ACTIVITY IN ESCHERICHIA-COLI [J].
DEAN, AM ;
DYKHUIZEN, DE ;
HARTL, DL .
GENETICAL RESEARCH, 1986, 48 (01) :1-8
[9]   Optimality and evolutionary tuning of the expression level of a protein [J].
Dekel, E ;
Alon, U .
NATURE, 2005, 436 (7050) :588-592
[10]   Bacteriophage-triggered defense systems: Phage adaptation and design improvements [J].
Djordjevic, GM ;
Klaenhammer, TR .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (11) :4370-4376