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ISWI chromatin remodeling complexes recruit NSD2 and H3K36me2 in pericentromeric heterochromatin.
- Source :
-
The Journal of cell biology [J Cell Biol] 2024 Aug 05; Vol. 223 (8). Date of Electronic Publication: 2024 May 06. - Publication Year :
- 2024
-
Abstract
- Histone H3 lysine36 dimethylation (H3K36me2) is generally distributed in the gene body and euchromatic intergenic regions. However, we found that H3K36me2 is enriched in pericentromeric heterochromatin in some mouse cell lines. We here revealed the mechanism of heterochromatin targeting of H3K36me2. Among several H3K36 methyltransferases, NSD2 was responsible for inducing heterochromatic H3K36me2. Depletion and overexpression analyses of NSD2-associating proteins revealed that NSD2 recruitment to heterochromatin was mediated through the imitation switch (ISWI) chromatin remodeling complexes, such as BAZ1B-SMARCA5 (WICH), which directly binds to AT-rich DNA via a BAZ1B domain-containing AT-hook-like motifs. The abundance and stoichiometry of NSD2, SMARCA5, and BAZ1B could determine the localization of H3K36me2 in different cell types. In mouse embryos, H3K36me2 heterochromatin localization was observed at the two- to four-cell stages, suggesting its physiological relevance.<br /> (© 2024 Goto et al.)
- Subjects :
- Animals
Humans
Mice
Adenosine Triphosphatases
Bromodomain Containing Proteins genetics
Bromodomain Containing Proteins metabolism
Centromere metabolism
Centromere genetics
Chromosomal Proteins, Non-Histone metabolism
Chromosomal Proteins, Non-Histone genetics
Methylation
Transcription Factors metabolism
Transcription Factors genetics
Chromatin Assembly and Disassembly
Heterochromatin metabolism
Heterochromatin genetics
Histone-Lysine N-Methyltransferase metabolism
Histone-Lysine N-Methyltransferase genetics
Histones metabolism
Histones genetics
Repressor Proteins metabolism
Repressor Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1540-8140
- Volume :
- 223
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- The Journal of cell biology
- Publication Type :
- Academic Journal
- Accession number :
- 38709169
- Full Text :
- https://doi.org/10.1083/jcb.202310084