Identification and characterization of novel proteins associated with CHD4

Chihiro Sakaguchi, Kazuya Ichihara, Akihiro Nita, Yuta Katayama, Keiichi I. Nakayama

Research output: Contribution to journalArticlepeer-review

Abstract

The CHD (chromodomain helicase DNA binding protein) family consists of nine chromatin remodeling factors that alter chromatin structure in an ATP-dependent manner. CHD4 contributes to the regulation of various cellular activities and processes including development through interaction with multiple proteins including formation of the NuRD (nucleosome remodeling and deacetylase activity) complex. Functions of CHD4 that appear not to be mediated by the NuRD complex or other known interactors have also been identified, however, suggesting the existence of unrecognized proteins that also associate with CHD4. We here generated HeLa-S3 and HEK293T cells with a knock-in allele for FLAG epitope-tagged CHD4 and used these cells to identify proteins that bind to CHD4 with the use of immunoprecipitation followed by liquid chromatography and tandem mass spectrometry. LCORL (ligand-dependent nuclear receptor corepressor like) and NOL4L (nucleolar protein 4 like) were reproducibly identified as novel CHD4 interactors. Furthermore, RNA-sequencing analysis of HEK293T cells depleted of CHD4, LCORL, or NOL4L revealed consistent up-regulation of genes related to the Notch signaling pathway. Our results thus suggest that both LCORL and NOL4L may cooperate with CHD4 to suppress the Notch pathway in mammalian cells.

Original languageEnglish
Pages (from-to)61-71
Number of pages11
JournalGenes to Cells
Volume27
Issue number1
DOIs
Publication statusPublished - Jan 2022

All Science Journal Classification (ASJC) codes

  • Genetics
  • Cell Biology

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