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HP1c regulates development and gut homeostasis by suppressing Notch signaling through Su(H).

Jin SunXia WangRong-Gang XuDecai MaoDa ShenXin WangYuhao QiuYuting HanXinyi LuYutong LiQinyun CheLi ZhengPing PengXuan KangRuibao ZhuYu JiaYinyin WangLu-Ping LiuZhijie ChangJun-Yuan JiZhao WangQingfei LiuShao LiFang-Lin SunJian-Quan Ni
Published in: EMBO reports (2021)
Notch signaling and epigenetic factors are known to play critical roles in regulating tissue homeostasis in most multicellular organisms, but how Notch signaling coordinates with epigenetic modulators to control differentiation remains poorly understood. Here, we identify heterochromatin protein 1c (HP1c) as an essential epigenetic regulator of gut homeostasis in Drosophila. Specifically, we observe that HP1c loss-of-function phenotypes resemble those observed after Notch signaling perturbation and that HP1c interacts genetically with components of the Notch pathway. HP1c represses the transcription of Notch target genes by directly interacting with Suppressor of Hairless (Su(H)), the key transcription factor of Notch signaling. Moreover, phenotypes caused by depletion of HP1c in Drosophila can be rescued by expressing human HP1γ, suggesting that HP1γ functions similar to HP1c in Drosophila. Taken together, our findings reveal an essential role of HP1c in normal development and gut homeostasis by suppressing Notch signaling.
Keyphrases
  • transcription factor
  • dna methylation
  • gene expression
  • genome wide
  • endothelial cells
  • cell proliferation
  • single cell
  • multidrug resistant
  • dna binding
  • protein kinase
  • wild type