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iChIP-SILAC analysis identifies epigenetic regulators of CpG methylation of the p16INK4A gene.
Fujita, Toshitsugu; Fujii, Hodaka.
Affiliation
  • Fujita T; Department of Biochemistry and Genome Biology, Hirosaki University Graduate School of Medicine, Japan.
  • Fujii H; Department of Biochemistry and Genome Biology, Hirosaki University Graduate School of Medicine, Japan.
FEBS Lett ; 598(9): 1094-1109, 2024 May.
Article in En | MEDLINE | ID: mdl-38627195
ABSTRACT
Allele-specific epigenetic events regulate the expression of specific genes such as tumor suppressor genes. Methods to biochemically identify epigenetic regulators remain limited. Here, we used insertional chromatin immunoprecipitation (iChIP) to address this issue. iChIP combined with quantitative mass spectrometry identified DNA methyltransferase 1 (DNMT1) and epigenetic regulators as proteins that potentially interact with a region of the p16INK4A gene that is CpG-methylated in one allele in HCT116 cells. Some of the identified proteins are involved in the CpG methylation of this region, and of these, DEAD-box helicase 24 (DDX24) contributes to CpG methylation by regulating the protein levels of DNMT1. Thus, iChIP is a useful method to identify proteins which bind to a target locus of interest.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: CpG Islands / DNA Methylation / Cyclin-Dependent Kinase Inhibitor p16 / Epigenesis, Genetic Limits: Humans Language: En Journal: FEBS Lett Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: CpG Islands / DNA Methylation / Cyclin-Dependent Kinase Inhibitor p16 / Epigenesis, Genetic Limits: Humans Language: En Journal: FEBS Lett Year: 2024 Document type: Article Affiliation country: Country of publication: