Nature Communications (Sep 2022)

WRN promotes bone development and growth by unwinding SHOX-G-quadruplexes via its helicase activity in Werner Syndrome

  • Yuyao Tian,
  • Wuming Wang,
  • Sofie Lautrup,
  • Hui Zhao,
  • Xiang Li,
  • Patrick Wai Nok Law,
  • Ngoc-Duy Dinh,
  • Evandro Fei Fang,
  • Hoi Hung Cheung,
  • Wai-Yee Chan

DOI
https://doi.org/10.1038/s41467-022-33012-6
Journal volume & issue
Vol. 13, no. 1
pp. 1 – 20

Abstract

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Short stature is a hallmark of Werner Syndrome, but the underlying mechanisms are not well studied. Here they report that WRN regulates bone development and growth by opening SHOX-G-quadruplexes via its helicase activity both in vitro and in vivo.