Nature Communications (Aug 2016)

Novel gene function revealed by mouse mutagenesis screens for models of age-related disease

  • Paul K. Potter,
  • Michael R. Bowl,
  • Prashanthini Jeyarajan,
  • Laura Wisby,
  • Andrew Blease,
  • Michelle E. Goldsworthy,
  • Michelle M. Simon,
  • Simon Greenaway,
  • Vincent Michel,
  • Alun Barnard,
  • Carlos Aguilar,
  • Thomas Agnew,
  • Gareth Banks,
  • Andrew Blake,
  • Lauren Chessum,
  • Joanne Dorning,
  • Sara Falcone,
  • Laurence Goosey,
  • Shelley Harris,
  • Andy Haynes,
  • Ines Heise,
  • Rosie Hillier,
  • Tertius Hough,
  • Angela Hoslin,
  • Marie Hutchison,
  • Ruairidh King,
  • Saumya Kumar,
  • Heena V. Lad,
  • Gemma Law,
  • Robert E. MacLaren,
  • Susan Morse,
  • Thomas Nicol,
  • Andrew Parker,
  • Karen Pickford,
  • Siddharth Sethi,
  • Becky Starbuck,
  • Femke Stelma,
  • Michael Cheeseman,
  • Sally H. Cross,
  • Russell G. Foster,
  • Ian J. Jackson,
  • Stuart N. Peirson,
  • Rajesh V. Thakker,
  • Tonia Vincent,
  • Cheryl Scudamore,
  • Sara Wells,
  • Aziz El-Amraoui,
  • Christine Petit,
  • Abraham Acevedo-Arozena,
  • Patrick M. Nolan,
  • Roger Cox,
  • Anne-Marie Mallon,
  • Steve D. M. Brown

DOI
https://doi.org/10.1038/ncomms12444
Journal volume & issue
Vol. 7, no. 1
pp. 1 – 13

Abstract

Read online

Random mutagenesis can uncover novel genes involved in phenotypic traits. Here the authors perform a large-scale phenotypic screen on over 100 mouse strains generated by ENU mutagenesis to identify mice with age-related diseases, which they attribute to specific mutations revealed by whole-genome sequencing.