Asxl1 exerts an antiproliferative effect on mouse lung maturation via epigenetic repression of the E2f1-Nmyc axis

Seungtae Moon, Sun Kyoung Im, Nackhyoung Kim, Hyesook Youn, Ui Hyun Park, Joo Yeon Kim, A. Reum Kim, So Jung An, Ji Hoon Kim, Woong Sun, Jin Taek Hwang, Eun Joo Kim, Soo Jong Um

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)


Although additional sex combs-like 1 (ASXL1) has been extensively described in hematologic malignancies, little is known about the molecular role of ASXL1 in organ development. Here, we show that Asxl1 ablation in mice results in postnatal lethality due to cyanosis, a respiratory failure. This lung defect is likely caused by higher proliferative potential and reduced expression of surfactant proteins, leading to reduced air space and defective lung maturation. By microarray analysis, we identified E2F1-responsive genes, including Nmyc, as targets repressed by Asxl1. Nmyc and Asxl1 are reciprocally expressed during the fetal development of normal mouse lungs, whereas Nmyc downregulation is impaired in Asxl1-deficient lungs. Together with E2F1 and ASXL1, host cell factor 1 (HCF-1), purified as an Asxl1-bound protein, is recruited to the E2F1-binding site of the Nmyc promoter. The interaction occurs between the C-terminal region of Asxl1 and the N-terminal Kelch domain of HCF-1. Trimethylation (me3) of histone H3 lysine 27 (H3K27) is enriched in the Nmyc promoter upon Asxl1 overexpression, whereas it is downregulated in Asxl1-deleted lung and -depleted A549 cells, similar to H3K9me3, another repressive histone marker. Overall, these findings suggest that Asxl1 modulates proliferation of lung epithelial cells via the epigenetic repression of Nmyc expression, deficiency of which may cause hyperplasia, leading to dyspnea.

Original languageEnglish
Article number1118
JournalCell Death and Disease
Issue number11
Publication statusPublished - 2018 Nov 1

Bibliographical note

Funding Information:
We thank Center for NeuroGenomics in Korea University for technical support for In Situ Hybridization and In-Hee Yang for assisting graphic summary. This study was supported in part by a grant from the Korea Food Research Institute funded by the Ministry of Science, ICT & Future Planning (E0150301-04) and a grant of the Bio & Medical Technology Development Program of the NRF funded by the Korean government, MSIT (2018M3A9H1023139).

Publisher Copyright:
© 2018, The Author(s).

ASJC Scopus subject areas

  • Immunology
  • Cellular and Molecular Neuroscience
  • Cell Biology
  • Cancer Research


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