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Phase separation of BuGZ regulates gut regeneration and aging through interaction with m 6 A regulators.

Qiaoqiao ZhangKai DengMengyou LiuShengye YangWei XuTong FengMinwen JieZhiming LiuXiao ShengHaiyang ChenHao Jiang
Published in: Nature communications (2023)
Exploring the role of phase separation in intracellular compartment formation is an active area of research. However, the associations of phase separation with intestinal stem cell (ISC)-dependent regeneration and aging remain unclear. Here, we demonstrate that BuGZ, a coacervating mitotic effector, shows age- and injury-associated condensation in Drosophila ISC nuclei during interphase. BuGZ condensation promotes ISC proliferation, affecting Drosophila gut repair and longevity. Moreover, m 6 A reader YT521-B acts as the transcriptional and functional downstream of BuGZ. The binding of YT521-B promotor or m 6 A writer Ime4/ Mettl14 to BuGZ controls its coacervation, indicating that the promotor may accelerate the phase transition of its binding transcription factor. Hence, we propose that phase separation and m 6 A regulators may be critical for ameliorating ISC-dependent gut regeneration and aging and requires further study.
Keyphrases
  • stem cells
  • transcription factor
  • dna binding
  • gene expression
  • wound healing
  • dendritic cells
  • binding protein
  • regulatory t cells
  • mesenchymal stem cells
  • reactive oxygen species
  • heat stress