Nature Communications (Oct 2021)

Rett syndrome linked to defects in forming the MeCP2/Rbfox/LASR complex in mouse models

  • Yan Jiang,
  • Xing Fu,
  • Yuhan Zhang,
  • Shen-Fei Wang,
  • Hong Zhu,
  • Wei-Kang Wang,
  • Lin Zhang,
  • Ping Wu,
  • Catherine C. L. Wong,
  • Jinsong Li,
  • Jinbiao Ma,
  • Ji-Song Guan,
  • Ying Huang,
  • Jingyi Hui

DOI
https://doi.org/10.1038/s41467-021-26084-3
Journal volume & issue
Vol. 12, no. 1
pp. 1 – 16

Abstract

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MeCP2 mutations can cause Rett syndrome, a severe childhood neurological disorder. Here the authors show that MeCP2 mediates the higher-order assembly of a large splicing complex Rbfox/LASR, which is disrupted in the mouse models of Rett syndrome.