Long-term experimental evolution in Escherichia coli.: XII.: DNA topology as a key target of selection

被引:105
作者
Crozat, E
Philippe, N
Lenski, RE
Geiselmann, J
Schneider, D
机构
[1] Univ Grenoble 1, Inst Jean Roget, Lab Adapt & Pathogenie Microorganismes, CNRS,UMR 5163, F-38041 Grenoble, France
[2] Michigan State Univ, Dept Microbiol & Mol Genet, E Lansing, MI 48824 USA
关键词
D O I
10.1534/genetics.104.035717
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The genetic bases of adaptation are being investigated in 12 populations of Escherichia coli, founded from a common ancestor and serially propagated for 20,000 generations, during which time they achieved substantial fitness gains. Each day, populations alternated between active growth and nutrient exhaustion. DNA supercoiling in bacteria is influenced by nutritional state, and DNA topology helps coordinate the overall pattern of gene expression in response to environmental changes. We therefore examined whether the genetic controls over supercoiling might have changed during the evolution experiment. Parallel changes in topology occurred in most populations, with the level of DNA supercoiling increasing, usually in the first 2000 generations. Two mutations in the topA and fis genes that control supercoiling were discovered in a population that served as the focus for further investigation. Moving the mutations, alone and in combination, into the ancestral background had an additive effect on supercoiling, and together they reproduced the net change in DNA topology observed in this population. Moreover, both mutations were beneficial in competition experiments. Clonal interference involving other beneficial DNA topology mutations was also detected. These findings define a new class of fitness-enhancing mutations and indicate that the control of DNA supercoiling can be a key target of selection in evolving bacterial populations.
引用
收藏
页码:523 / 532
页数:10
相关论文
共 56 条
[1]   Mechanism of transcriptional activation by FIS: Role of core promoter structure and DNA topology [J].
Auner, H ;
Buckle, M ;
Deufel, A ;
Kutateladze, T ;
Lazarus, L ;
Mavathur, R ;
Muskhelishvili, G ;
Pemberton, I ;
Schneider, R ;
Travers, A .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 331 (02) :331-344
[2]   CHANGES IN THE LINKING NUMBER OF SUPERCOILED DNA ACCOMPANY GROWTH TRANSITIONS IN ESCHERICHIA-COLI [J].
BALKE, VL ;
GRALLA, JD .
JOURNAL OF BACTERIOLOGY, 1987, 169 (10) :4499-4506
[3]   AN OVERLAP BETWEEN OSMOTIC AND ANAEROBIC STRESS RESPONSES - A POTENTIAL ROLE FOR DNA SUPERCOILING IN THE COORDINATE REGULATION OF GENE-EXPRESSION [J].
BHRIAIN, NN ;
DORMAN, CJ ;
HIGGINS, CF .
MOLECULAR MICROBIOLOGY, 1989, 3 (07) :933-942
[4]   USE OF SITE-SPECIFIC RECOMBINATION AS A PROBE OF DNA-STRUCTURE AND METABOLISM INVIVO [J].
BLISKA, JB ;
COZZARELLI, NR .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 194 (02) :205-218
[5]   ALLELIC EXCHANGE IN ESCHERICHIA-COLI USING THE BACILLUS-SUBTILIS SACB GENE AND A TEMPERATURE-SENSITIVE PSC101 REPLICON [J].
BLOMFIELD, IC ;
VAUGHN, V ;
REST, RF ;
EISENSTEIN, BI .
MOLECULAR MICROBIOLOGY, 1991, 5 (06) :1447-1457
[6]   STRUCTURE OF PLECTONEMICALLY SUPERCOILED DNA [J].
BOLES, TC ;
WHITE, JH ;
COZZARELLI, NR .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 213 (04) :931-951
[7]  
Bull JJ, 1997, GENETICS, V147, P1497
[8]   DNA topoisomerases: Structure, function, and mechanism [J].
Champoux, JJ .
ANNUAL REVIEW OF BIOCHEMISTRY, 2001, 70 :369-413
[9]   Identification of active site residues in Escherichia coli DNA topoisomerase I [J].
Chen, SJ ;
Wang, JC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (11) :6050-6056
[10]   Parallel changes in qene expression after 20,000 generations of evolution in Escherichia coli [J].
Cooper, TF ;
Rozen, DE ;
Lenski, RE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (03) :1072-1077