<scp>CTCF</scp> ‐Binding Sites Demarcate Chromatin Domains Enriched With Histone <scp>H3K9me2</scp> or <scp>H3K9me3</scp> and Restrict the Spreading of These Modifications in Human Cells

CTCF-binding sites are frequently found at the boundaries of chromatin domains enriched with specific histone modifications in vertebrate genomes, where they function as barriers that limit the spreading of these modifications. However, their role in domains marked by H3K9me2 or H3K9me3 remains poorly understood. In this study, we analyzed CTCF-binding sites and the distribution of H3K9me2 and H3K9me3 around them in human K562 cells, and investigated the spreading of these modifications following CTCF depletion. Genome-wide analysis revealed that certain CTCF-binding sites are located at the boundaries of chromatin domains enriched with H3K9me2 or H3K9me3. Upon loss of CTCF binding, both modifications spread to neighboring chromatin at over half of the boundaries delimiting highly and distinctly enriched domains. Boundaries where such spreading did not occur were flanked by chromatin in a more active state compared to those where spreading occurred. Gene transcription was significantly reduced in neighboring regions where H3K9me2 or H3K9me3 had spread. Further comprehensive analysis revealed that this transcriptional reduction was specifically associated with the spread of H3K9me2. These findings suggest that CTCF-binding sites demarcate chromatin domains enriched with H3K9me2 or H3K9me3 and act as barriers to restrict the spread of these modifications in mammalian cells. Notably, the spread of H3K9me2 appears to play a primary role in transcriptional repression.

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Publication Details

Journal
The FASEB Journal
Published
2026-01-03
DOI
https://doi.org/10.1096/fj.202502813r
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
0.00

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article

CTCF ‐Binding Sites Demarcate Chromatin Domains Enriched With Histone H3K9me2 or H3K9me3 and Restrict the Spreading of These Modifications in Human Cells

Jin Joo Kang, AeRi Kim, Kyung‐Ju Shin
The FASEB Journal
Genomics and Chromatin Dynamics
article

CTCF ‐Binding Sites Demarcate Chromatin Domains Enriched With Histone H3K9me2 or H3K9me3 and Restrict the Spreading of These Modifications in Human Cells

Jin Joo Kang, AeRi Kim, Kyung‐Ju Shin
article en

Abstract

CTCF-binding sites are frequently found at the boundaries of chromatin domains enriched with specific histone modifications in vertebrate genomes, where they function as barriers that limit the spreading of these modifications. However, their role in domains marked by H3K9me2 or H3K9me3 remains poorly understood. In this study, we analyzed CTCF-binding sites and the distribution of H3K9me2 and H3K9me3 around them in human K562 cells, and investigated the spreading of these modifications following CTCF depletion. Genome-wide analysis revealed that certain CTCF-binding sites are located at the boundaries of chromatin domains enriched with H3K9me2 or H3K9me3. Upon loss of CTCF binding, both modifications spread to neighboring chromatin at over half of the boundaries delimiting highly and distinctly enriched domains. Boundaries where such spreading did not occur were flanked by chromatin in a more active state compared to those where spreading occurred. Gene transcription was significantly reduced in neighboring regions where H3K9me2 or H3K9me3 had spread. Further comprehensive analysis revealed that this transcriptional reduction was specifically associated with the spread of H3K9me2. These findings suggest that CTCF-binding sites demarcate chromatin domains enriched with H3K9me2 or H3K9me3 and act as barriers to restrict the spread of these modifications in mammalian cells. Notably, the spread of H3K9me2 appears to play a primary role in transcriptional repression.

The FASEB JournalVol. 40(1)
Pusan National University (KR)
National Research Foundation, National Research Foundation of Korea, Ministry of Science and ICT, South Korea
Openalex Percentile: Top 98%
Genomics and Chromatin Dynamics
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