Nature Communications (Sep 2021)

Structure of a Ty1 restriction factor reveals the molecular basis of transposition copy number control

  • Matthew A. Cottee,
  • Sean L. Beckwith,
  • Suzanne C. Letham,
  • Sarah J. Kim,
  • George R. Young,
  • Jonathan P. Stoye,
  • David J. Garfinkel,
  • Ian A. Taylor

DOI
https://doi.org/10.1038/s41467-021-25849-0
Journal volume & issue
Vol. 12, no. 1
pp. 1 – 17

Abstract

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In Saccharomyces cerevisiae, unchecked proliferation of Ty1 retrotransposons is controlled by the process of copy number control (CNC), which requires the p22/p18 protein, translated from an internal transcript within the Ty1 GAG gene. Here, the authors present the 2.8 Å crystal structure of a minimal p18 from Ty1-Gag that is able to restrict Ty1 transposition and identify two dimer interfaces in p18, whose roles were probed by mutagenesis both in vitro and in vivo. As p22/p18 contains only one of two conserved domains required for retroelement Gag assembly, they propose that p22/p18-Gag interactions block the Ty1 virus-like particle assembly pathway, resulting in defective particles incapable of supporting retrotransposition.