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  1. Artikel ; Online: Lysine-36 of Drosophila histone H3.3 supports adult longevity.

    Brown, John C / McMichael, Benjamin D / Vandadi, Vasudha / Mukherjee, Aadit / Salzler, Harmony R / Matera, A Gregory

    G3 (Bethesda, Md.)

    2024  Band 14, Heft 4

    Abstract: Aging is a multifactorial process that disturbs homeostasis, increases disease susceptibility, and ultimately results in death. Although the definitive set of molecular mechanisms responsible for aging remain to be discovered, epigenetic change over time ...

    Abstract Aging is a multifactorial process that disturbs homeostasis, increases disease susceptibility, and ultimately results in death. Although the definitive set of molecular mechanisms responsible for aging remain to be discovered, epigenetic change over time is proving to be a promising piece of the puzzle. Several post-translational histone modifications have been linked to the maintenance of longevity. Here, we focus on lysine-36 of the replication-independent histone protein, H3.3 (H3.3K36). To interrogate the role of this residue in Drosophila developmental gene regulation, we generated a lysine-to-arginine mutant that blocks the activity of its cognate-modifying enzymes. We found that an H3.3BK36R mutation causes a significant reduction in adult lifespan, accompanied by dysregulation of the genomic and transcriptomic architecture. Transgenic co-expression of wild-type H3.3B completely rescues the longevity defect. Because H3.3 is known to accumulate in nondividing tissues, we carried out transcriptome profiling of young vs aged adult fly heads. The data show that loss of H3.3K36 results in age-dependent misexpression of NF-κB and other innate immune target genes, as well as defects in silencing of heterochromatin. We propose H3.3K36 maintains the postmitotic epigenomic landscape, supporting longevity by regulating both pericentric and telomeric retrotransposons and by suppressing aberrant immune signaling.
    Mesh-Begriff(e) Animals ; Drosophila/genetics ; Drosophila/metabolism ; Heterochromatin ; Histones/genetics ; Histones/metabolism ; Longevity/genetics ; Lysine/metabolism
    Chemische Substanzen Heterochromatin ; Histones ; Lysine (K3Z4F929H6)
    Sprache Englisch
    Erscheinungsdatum 2024-02-17
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2629978-1
    ISSN 2160-1836 ; 2160-1836
    ISSN (online) 2160-1836
    ISSN 2160-1836
    DOI 10.1093/g3journal/jkae030
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel: Lysine-36 of

    Brown, John C / McMichael, Benjamin D / Vandadi, Vasudha / Mukherjee, Aadit / Salzler, Harmony R / Matera, A Gregory

    bioRxiv : the preprint server for biology

    2023  

    Abstract: Aging is a multifactorial process that disturbs homeostasis, increases disease susceptibility, and ultimately results in death. Although the definitive set of molecular mechanisms responsible for aging remain to be discovered, epigenetic change over time ...

    Abstract Aging is a multifactorial process that disturbs homeostasis, increases disease susceptibility, and ultimately results in death. Although the definitive set of molecular mechanisms responsible for aging remain to be discovered, epigenetic change over time is proving to be a promising piece of the puzzle. Several posttranslational histone modifications (PTMs) have been linked to the maintenance of longevity. Here, we focus on lysine-36 of the replication-independent histone protein, H3.3 (H3.3K36). To interrogate the role of this residue in
    Sprache Englisch
    Erscheinungsdatum 2023-12-13
    Erscheinungsland United States
    Dokumenttyp Preprint
    DOI 10.1101/2023.09.28.559962
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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