Gene order constrains adaptation in bacteriophage T7

被引:22
作者
Springman, R
Badgett, MR
Molineux, IJ
Bull, JJ
机构
[1] Univ Texas, Sect Mol Genet & Microbiol, Austin, TX 78712 USA
[2] Univ Texas, Sect Integrat Biol, Austin, TX 78712 USA
[3] Univ Texas, Inst Mol & Cellular Biol, Austin, TX 78712 USA
关键词
experimental evolution; genome evolution; microbial evolution; molecular evolution; bacteriophage;
D O I
10.1016/j.virol.2005.07.008
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The order of genes in the genome is commonly thought to have functional significance for gene regulation and fitness but has not heretofore been tested experimentally. We adapted a bacteriophage T7 variant harboring an ectopically positioned RNA polymerase gene to determine whether it could regain the fitness of the wild type. Two replicate lines maintained the starting gene order and showed only modest recovery of fitness, despite the accumulation of over a dozen mutations. In both lines, a mutation in the early terminator signal is responsible for the majority of the fitness recovery. In a third line, the phage evolved a new gene order, restoring the wild-type position of the RNA polymerase gene but also displacing several other genes to ectopic locations. Due to the recombination, the fitness of this replicate was the highest obtained but it falls short of the wild type adapted to the same growth conditions. The large benefits afforded by the terminator mutation and the recombination are explicable in terms of T7 biology, whereas several mutations with lesser benefits are not easily accounted for. These results support the premise that gene order is important to fitness and that wild-type fitness is not rapidly re-evolved in reorganized genomes. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:141 / 152
页数:12
相关论文
共 59 条
[1]   Development of genetic circuitry exhibiting toggle switch or oscillatory behavior in Escherichia coli [J].
Atkinson, MR ;
Savageau, MA ;
Myers, JT ;
Ninfa, AJ .
CELL, 2003, 113 (05) :597-607
[2]   Regulatory circuit design and evolution using phage λ [J].
Atsumi, S ;
Little, JW .
GENES & DEVELOPMENT, 2004, 18 (17) :2086-2094
[3]   Phenotypic consequences of rearranging the P, M, and G genes of vesicular stomatitis virus [J].
Ball, LA ;
Pringle, CR ;
Flanagan, B ;
Perepelitsa, VP ;
Wertz, GW .
JOURNAL OF VIROLOGY, 1999, 73 (06) :4705-4712
[4]   Phages and the evolution of bacterial pathogens:: From genomic rearrangements to lysogenic conversion [J].
Brüssow, H ;
Canchaya, C ;
Hardt, WD .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2004, 68 (03) :560-+
[5]   Phages of dairy bacteria [J].
Brüssow, H .
ANNUAL REVIEW OF MICROBIOLOGY, 2001, 55 :283-303
[6]  
Bull JJ, 2004, EVOLUTION, V58, P692
[7]   Prophages and bacterial genomics: what have we learned so far? [J].
Casjens, S .
MOLECULAR MICROBIOLOGY, 2003, 49 (02) :277-300
[8]  
Chamberlin M., 1982, ENZYMES, V15, P87
[9]  
Chamberlin M.J., 1982, ENZYMES, VXV, P61
[10]   FUNCTIONAL IMPORTANCE OF SEQUENCE IN THE STEM-LOOP OF A TRANSCRIPTION TERMINATOR [J].
CHENG, SWC ;
LYNCH, EC ;
LEASON, KR ;
COURT, DL ;
SHAPIRO, BA ;
FRIEDMAN, DI .
SCIENCE, 1991, 254 (5035) :1205-1207