Experimental genomic evolution: Extensive compensation for loss of DNA ligase activity in a virus

被引:56
作者
Rokyta, D
Badgett, MR
Molineux, IJ
Bull, JJ [1 ]
机构
[1] Univ Texas, Sect Integrat Biol, Austin, TX 78712 USA
[2] Univ Texas, Sect Mol Genet & Microbiol, Austin, TX 78712 USA
[3] Univ Texas, Inst Cellular & Mol Biol, Austin, TX 78712 USA
关键词
microbe; evolution; bacteriophage; genomics; compensatory evolution; resistance;
D O I
10.1093/oxfordjournals.molbev.a004076
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Deletion of the viral lipase gene drastically reduced the fitness of bacteriophage T7 on a ligase-deficient host. Viral evolution recovered much of this fitness during long-term passage, but the final fitness remained below that of the intact virus. Compensatory changes occurred chiefly in genes involved in DNA metabolism: the viral endonuclease, helicase, and DNA polymerase. Two other compensatory changes of unknown function also Occurred. Using a method to distinguish compensatory mutations from other beneficial mutations, five additional substitutions from the recovery were shown to enhance adaptation to culture conditions and were not compensatory for thee deletion. In contrast to the few previous studies of viral recovery from deletions, the compensatory changes in T7 did not restore the deletion or duplicate major regions of the genome. The ability of this deleted genome to recover much of the lost fitness via mutations in its remaining genes reveals a considerable evolutionary potential to modify the interactions of its elements in maintaining all essential set of functions.
引用
收藏
页码:230 / 238
页数:9
相关论文
共 37 条
[1]   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
[2]   A UNIQUE DEOXYGUANOSINE TRIPHOSPHATASE IS RESPONSIBLE FOR THE OPTA1 PHENOTYPE OF ESCHERICHIA-COLI [J].
BEAUCHAMP, BB ;
RICHARDSON, CC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (08) :2563-2567
[3]   Genetic instability of live, attenuated human immunodeficiency virus type 1 vaccine strains [J].
Berkhout, B ;
Verhoef, K ;
van Wamel, JLB ;
Back, NKT .
JOURNAL OF VIROLOGY, 1999, 73 (02) :1138-1145
[4]   Effects of environment on compensatory mutations to ameliorate costs of antibiotic resistance [J].
Björkman, J ;
Nagaev, I ;
Berg, OG ;
Hughes, D ;
Andersson, DI .
SCIENCE, 2000, 287 (5457) :1479-1482
[5]   Exploring the new world of the genome with DNA microarrays [J].
Brown, PO ;
Botstein, D .
NATURE GENETICS, 1999, 21 (Suppl 1) :33-37
[6]   Big-benefit mutations in a bacteriophage inhibited with heat [J].
Bull, JJ ;
Badgett, MR ;
Wichman, HA .
MOLECULAR BIOLOGY AND EVOLUTION, 2000, 17 (06) :942-950
[7]  
Burch CL, 1999, GENETICS, V151, P921
[8]   THE 2-HYBRID SYSTEM - A METHOD TO IDENTIFY AND CLONE GENES FOR PROTEINS THAT INTERACT WITH A PROTEIN OF INTEREST [J].
CHIEN, CT ;
BARTEL, PL ;
STERNGLANZ, R ;
FIELDS, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (21) :9578-9582
[9]   Statistical modeling and analysis of the LAGLIDADG family of site-specific endonucleases and identification of an intein that encodes a site-specific endonuclease of the HNH family [J].
Dalgaard, JZ ;
Klar, AJ ;
Moser, MJ ;
Holley, WR ;
Chatterjee, A ;
Mian, IS .
NUCLEIC ACIDS RESEARCH, 1997, 25 (22) :4626-4638
[10]  
Drake JW, 1998, GENETICS, V148, P1667