53BP1 recruitment to DSBs

Biomarker

1 paper studies it3 findings

  • Cells1

Interventions

1

Trichostatin A

no changein human cells1

1 study
  1. Trichostatin A has no effect on 53BP1 recruitment to DSBs in human cells.

    “Induced hyperacetylation of late passage (LP) cells using trichostatin A increased H4K16Ac levels but did not ameliorate 53BP1 recruitment.”

    Cellsin late passage cells

    Role of H4K16 acetylation in 53BP1 recruitment to double-strand break sites in in vitro aged cells

    Biogerontology

More on Trichostatin A

Upstream

1

KAT8

is required forin human cells1

1 study
  1. KAT8 is required for 53BP1 recruitment to DSBs in human cells.

    “Instead, deacetylation induced by MOF silencing reduced H4K16Ac levels and compromised 53BP1 recruitment in both EP and LP cells.”

    Cellsshown by silencing in EP and LP cells

    Role of H4K16 acetylation in 53BP1 recruitment to double-strand break sites in in vitro aged cells

    Biogerontology

More on KAT8

Associations

1

H4K16ac

downin human cells1

1 study
  1. H4K16ac is associated with 53BP1 recruitment to DSBs in human cells.

    “In vitro aged Human Dermal Fibroblasts (HDFs) display lower levels of H4K16A that correlate with reduced recruitment of 53BP1 to basal DSBs.”

    Cellsin in vitro aged cells

    Role of H4K16 acetylation in 53BP1 recruitment to double-strand break sites in in vitro aged cells

    Biogerontology

More on H4K16ac

Latest