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

Abstract

Understanding how new functions evolve has been of long-standing interest. However, the number of mutations needed to evolve a key innovation is rarely known, or whether other sets of mutations would also suffice, whether the intermediate steps are driven by natural selection, or how contingent the outcome is on steps along the way. Meyer et al. (p. 428 ; see the Perspective by Thompson ) answer these questions for a case in which phage lambda evolved the ability to infect its host Escherichia coli through a novel receptor. This shift required four mutations, which accumulated under natural selection in concert with coevolution of the host. However, when Tenaillon et al. (p. 457 ) exposed 115 lines of E. coli to high temperature and sequenced them, adaptation occurred through many different genetic paths, showing parallelism at the level of genes and interacting protein complexes, but only rarely at the nucleotide level. Thus, epistasis—nonadditive genetic interaction—is likely to play an important part in the process of adaptation to this environment.

Document Details

Document Type
Pub Defense Publication
Publication Date
Jan 27, 2012
Source ID
10.1126/science.1214449

Entities

People

  • Devin T. Dobias
  • Jeffrey E Barrick
  • Joshua Weitz
  • Justin R. Meyer
  • Richard E. Lenski
  • Ryan T. Quick

Organizations

  • Defense Advanced Research Projects Agency
  • Georgia Tech
  • Michigan State University
  • National Institutes of Health
  • National Science Foundation
  • University of Texas at Austin
  • Washington University in St. Louis

Tags

Fields of Study

  • Biology

Readers

  • Molecular and Cellular Biochemistry
  • Molecular and genetic basis of cancer.
  • Theoretical Analysis.

Technology Areas

  • Biotechnology