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Dual function of PHF16 in reinstating homeostasis of murine intestinal epithelium after crypt regeneration.
Ahn, Jun-Yeong; Kim, Somi; Rok Kim, Chang; Lee, Ji-Hyun; Kim, Jong Min; Klompstra, Thomas M; Ha Choi, Yoon; Jeon, Yoon; Na, Yongwoo; Kim, Jong-Seo; Okada, Yuki; Lee, Ho; Kim, Ik Soo; Kim, Jong Kyoung; Koo, Bon-Kyoung; Baek, Sung Hee.
Afiliação
  • Ahn JY; Creative Research Initiatives Center for Epigenetic Code and Diseases, Seoul National University, Seoul 08826, South Korea; School of Biological Sciences, Seoul National University, Seoul 08826, South Korea.
  • Kim S; Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang 37673, South Korea.
  • Rok Kim C; Creative Research Initiatives Center for Epigenetic Code and Diseases, Seoul National University, Seoul 08826, South Korea; School of Biological Sciences, Seoul National University, Seoul 08826, South Korea.
  • Lee JH; Center for Genome Engineering, Institute for Basic Science, 55, Expo-ro, Yuseong-gu, Daejeon 34126, South Korea.
  • Kim JM; Creative Research Initiatives Center for Epigenetic Code and Diseases, Seoul National University, Seoul 08826, South Korea; School of Biological Sciences, Seoul National University, Seoul 08826, South Korea.
  • Klompstra TM; Center for Genome Engineering, Institute for Basic Science, 55, Expo-ro, Yuseong-gu, Daejeon 34126, South Korea.
  • Ha Choi Y; Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang 37673, South Korea.
  • Jeon Y; Department of Cancer Biomedical Science, Graduate School of Cancer Science and Policy, National Cancer Center, Goyang 10408, South Korea.
  • Na Y; School of Biological Sciences, Seoul National University, Seoul 08826, South Korea.
  • Kim JS; School of Biological Sciences, Seoul National University, Seoul 08826, South Korea; Center for RNA Research, Institute for Basic Science, School of Biological Sciences, Seoul National University, Seoul 08826, South Korea.
  • Okada Y; Laboratory of Pathology and Development, Institute for Quantitative Biosciences, The University of Tokyo, Tokyo 113-0032, Japan.
  • Lee H; Department of Cancer Biomedical Science, Graduate School of Cancer Science and Policy, National Cancer Center, Goyang 10408, South Korea.
  • Kim IS; Department of Microbiology, Gachon University College of Medicine, Incheon 21999, South Korea. Electronic address: iksookim@gachon.ac.kr.
  • Kim JK; Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang 37673, South Korea; Institute for Convergence Research and Education in Advanced Technology, Yonsei University, Seoul 03722, South Korea. Electronic address: blkimjk@postech.ac.kr.
  • Koo BK; Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang 37673, South Korea; Center for Genome Engineering, Institute for Basic Science, 55, Expo-ro, Yuseong-gu, Daejeon 34126, South Korea. Electronic address: koobk@ibs.re.kr.
  • Baek SH; Creative Research Initiatives Center for Epigenetic Code and Diseases, Seoul National University, Seoul 08826, South Korea; School of Biological Sciences, Seoul National University, Seoul 08826, South Korea. Electronic address: sbaek@snu.ac.kr.
Dev Cell ; 2024 Aug 27.
Article em En | MEDLINE | ID: mdl-39232563
ABSTRACT
Intestinal stem cells (ISCs) are highly vulnerable to damage, being in a constant state of proliferation. Reserve stem cells repair the intestinal epithelium following damage-induced ablation of ISCs. Here, we report that the epigenetic regulator plant homology domain (PHD) finger protein 16 (PHF16) restores homeostasis of the intestinal epithelium after initial damage-induced repair. In Phf16-/Y mice, revival stem cells (revSCs) showed defects in exiting the regenerative state, and intestinal crypt regeneration failed even though revSCs were still induced in response to tissue damage, as observed by single-cell RNA sequencing (scRNA-seq). Analysis of Phf16-/Y intestinal organoids by RNA sequencing (RNA-seq) and ATAC sequencing identified that PHF16 restores homeostasis of the intestinal epithelium by inducing retinoic acid receptor (RAR)/retinoic X receptor (RXR) target genes through HBO1-mediated histone H3K14 acetylation, while at the same time counteracting YAP/TAZ activity by ubiquitination of CDC73. Together, our findings demonstrate the importance of timely suppression of regenerative activity by PHF16 for the restoration of gut homeostasis after acute tissue injury.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article