| Literature DB >> 33594776 |
Jin Sun1,2, Xia Wang1,3, Rong-Gang Xu1, Decai Mao1,4, Da Shen1, Xin Wang5, Yuhao Qiu1,6, Yuting Han1, Xinyi Lu1, Yutong Li1, Qinyun Che1, Li Zheng1, Ping Peng1,6, Xuan Kang7, Ruibao Zhu1,6, Yu Jia1,6, Yinyin Wang8, Lu-Ping Liu1, Zhijie Chang8, Jun-Yuan Ji9, Zhao Wang10, Qingfei Liu10, Shao Li5, Fang-Lin Sun7, Jian-Quan Ni1,11.
Abstract
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.Entities:
Keywords: Drosophila development; HP1c; Notch signaling pathway; Su(H); gut homeostasis
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Year: 2021 PMID: 33594776 PMCID: PMC8024896 DOI: 10.15252/embr.202051298
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807