Repeatability and Contingency in the Evolution of a Key Innovation in Phage Lambda

被引:330
作者
Meyer, Justin R. [1 ,2 ]
Dobias, Devin T. [3 ]
Weitz, Joshua S. [4 ,5 ]
Barrick, Jeffrey E. [2 ,6 ]
Quick, Ryan T. [7 ]
Lenski, Richard E. [1 ,2 ,7 ]
机构
[1] Michigan State Univ, Dept Zool, E Lansing, MI 48824 USA
[2] Michigan State Univ, BEACON Ctr Study Evolut Act, E Lansing, MI 48824 USA
[3] Washington Univ, Dept Biol, St Louis, MO 63130 USA
[4] Georgia Inst Technol, Sch Biol, Atlanta, GA 30332 USA
[5] Georgia Inst Technol, Sch Phys, Atlanta, GA 30332 USA
[6] Univ Texas Austin, Dept Chem & Biochem, Inst Cellular & Mol Biol, Austin, TX 78712 USA
[7] Michigan State Univ, Dept Microbiol & Mol Genet, E Lansing, MI 48824 USA
关键词
BACTERIOPHAGE-LAMBDA; MEMBRANE-PROTEINS; RECEPTOR; ADAPTATION; MECHANISMS; MALTOPORIN; DYNAMICS; CONSISTS; BINDING; SURFACE;
D O I
10.1126/science.1214449
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The processes responsible for the evolution of key innovations, whereby lineages acquire qualitatively new functions that expand their ecological opportunities, remain poorly understood. We examined how a virus, bacteriophage l, evolved to infect its host, Escherichia coli, through a novel pathway. Natural selection promoted the fixation of mutations in the virus's host-recognition protein, J, that improved fitness on the original receptor, LamB, and set the stage for other mutations that allowed infection through a new receptor, OmpF. These viral mutations arose after the host evolved reduced expression of LamB, whereas certain other host mutations prevented the phage from evolving the new function. This study shows the complex interplay between genomic processes and ecological conditions that favor the emergence of evolutionary innovations.
引用
收藏
页码:428 / 432
页数:5
相关论文
共 47 条
  • [1] [Anonymous], 2004, Adaptive speciation
  • [2] [Anonymous], 1872, The origin of species
  • [3] [Anonymous], 1999, The genetical theory of natural selection: a complete variorum edition
  • [4] Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants:: the Keio collection
    Baba, Tomoya
    Ara, Takeshi
    Hasegawa, Miki
    Takai, Yuki
    Okumura, Yoshiko
    Baba, Miki
    Datsenko, Kirill A.
    Tomita, Masaru
    Wanner, Barry L.
    Mori, Hirotada
    [J]. MOLECULAR SYSTEMS BIOLOGY, 2006, 2 (1) : 2006.0008
  • [5] Interaction of bacteriophage Lambda with its cell surface receptor: An in vitro study of binding of the viral tail protein gpJ to LamB (Maltoporin)
    Berkane, E
    Orlik, F
    Stegmeier, JF
    Charbit, A
    Winterhalter, M
    Benz, R
    [J]. BIOCHEMISTRY, 2006, 45 (08) : 2708 - 2720
  • [6] Historical contingency and the evolution of a key innovation in an experimental population of Escherichia coli
    Blount, Zachary D.
    Borland, Christina Z.
    Lenski, Richard E.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (23) : 7899 - 7906
  • [7] Linking genetic change to community evolution: insights from studies of bacteria and bacteriophage
    Bohannan, BJM
    Lenski, RE
    [J]. ECOLOGY LETTERS, 2000, 3 (04) : 362 - 377
  • [8] EXPLANATIONS ACCOUNTING FOR TRANSDUCTION BY BACTERIOPHAGE-GAMMA IN MALTOSE NEGATIVE BACTERIOPHAGE GAMMA-RESISTANT MUTANTS OF ESCHERICHIA-COLI K-12
    BRAUNBRETON, C
    HOFNUNG, M
    [J]. MOLECULAR & GENERAL GENETICS, 1978, 159 (02): : 143 - 149
  • [9] Cairns J., 2007, Phage and the Origins of Molecular Biology
  • [10] Mechanisms causing rapid and parallel losses of ribose catabolism in evolving populations of Escherichia coli B
    Cooper, VS
    Schneider, D
    Blot, M
    Lenski, RE
    [J]. JOURNAL OF BACTERIOLOGY, 2001, 183 (09) : 2834 - 2841