Journal Article DKFZ-2025-02392

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Histone H1.5 binds over splice sites in chromatin and regulates alternative splicing.

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2019
Oxford Univ. Press Oxford

Nucleic acids research 47(12), 6145 - 6159 () [10.1093/nar/gkz338]
 GO

Abstract: Chromatin organization and epigenetic markers influence splicing, though the magnitudes of these effects and the mechanisms are largely unknown. Here, we demonstrate that linker histone H1.5 influences mRNA splicing. We observed that linker histone H1.5 binds DNA over splice sites of short exons in human lung fibroblasts (IMR90 cells). We found that association of H1.5 with these splice sites correlated with the level of inclusion of alternatively spliced exons. Exons marked by H1.5 had more RNA polymerase II (RNAP II) stalling near the 3' splice site than did exons not associated with H1.5. In cells depleted of H1.5, we showed that the inclusion of five exons evaluated decreased and that RNAP II levels over these exons were also reduced. Our findings indicate that H1.5 is involved in regulation of splice site selection and alternative splicing, a function not previously demonstrated for linker histones.

Keyword(s): Alternative Splicing (MeSH) ; Cell Line (MeSH) ; Chromatin: metabolism (MeSH) ; DNA: metabolism (MeSH) ; Exons (MeSH) ; Histones: metabolism (MeSH) ; Humans (MeSH) ; Introns (MeSH) ; RNA Polymerase II: metabolism (MeSH) ; RNA Splice Sites (MeSH) ; Chromatin ; H1-5 protein, human ; Histones ; RNA Splice Sites ; DNA ; RNA Polymerase II

Classification:

Note: #DKFZ-MOST-Ca175#


Database coverage:
Medline ; DOAJ ; Article Processing Charges ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; DOAJ Seal ; Essential Science Indicators ; Fees ; IF >= 10 ; JCR ; NationallizenzNationallizenz ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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External Publications > Coordinated Projects
Institute Collections > W500

 Record created 2025-11-13, last modified 2025-11-13


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