Linker histones consolidate heterogenous nucleosome fiber contacts by linking together multiple nucleosomes

The consensus mode for linker histone (H1) association coincides with 'on-dyad' binding to an individual nucleosome, making it challenging to rationalize the chromatin dynamics and compacting activities of H1 in the context of a highly heterogeneous structural scaffold. Here, we investigate the activity of the somatic H1 variants by conducting crystallographic analysis of nucleosomal assemblies and characterization of nucleosome array condensates, which recapitulate long-range nucleosome fiber interactions in chromatin. H1 is observed to associate variant-dependently with nucleosomes through a diversity of binding modes that include linking multiple nucleosomes/fibers together. Binding versatility is facilitated by the proclivity of the H1 globular domain to recognize DNA structural motifs, which are similar between an individual nucleosome and specific niches within clusters of nucleosomes. We propose that linker histones support a structurally and functionally complex repertoire for chromatin regulation by assuming a variety of context-and variant-dependent DNA binding modes.

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Journal
Nature Communications
Published
2026-03-05
DOI
https://doi.org/10.1038/s41467-026-69842-x
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
0.00

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article

Linker histones consolidate heterogenous nucleosome fiber contacts by linking together multiple nucleosomes

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Genomics and Chromatin Dynamics
article

Linker histones consolidate heterogenous nucleosome fiber contacts by linking together multiple nucleosomes

Zenita Adhireksan, Sivaraman Padavattan, Phoi Leng Lee, Qiuye Bao, Gabriela E. Davey, Jeffrey C. Hansen, Deepti Sharma, Curtis A. Davey
article en

Abstract

The consensus mode for linker histone (H1) association coincides with 'on-dyad' binding to an individual nucleosome, making it challenging to rationalize the chromatin dynamics and compacting activities of H1 in the context of a highly heterogeneous structural scaffold. Here, we investigate the activity of the somatic H1 variants by conducting crystallographic analysis of nucleosomal assemblies and characterization of nucleosome array condensates, which recapitulate long-range nucleosome fiber interactions in chromatin. H1 is observed to associate variant-dependently with nucleosomes through a diversity of binding modes that include linking multiple nucleosomes/fibers together. Binding versatility is facilitated by the proclivity of the H1 globular domain to recognize DNA structural motifs, which are similar between an individual nucleosome and specific niches within clusters of nucleosomes. We propose that linker histones support a structurally and functionally complex repertoire for chromatin regulation by assuming a variety of context-and variant-dependent DNA binding modes.

Nature Communications
Jagiellonian University (PL), Nanyang Technological University (SG), National Institute of Mental Health and Neurosciences (IN), Colorado State University (US)
Paul Scherrer Institut, Ministry of Education, India
Openalex Percentile: Top 33%
Genomics and Chromatin Dynamics
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