53BP1 recruitment to DSBs
1 paper studies it3 findings
- Cells1
Interventions
1Trichostatin A
no changein human cells1
1 study
Trichostatin A
no changein human cells1
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
Upstream
1KAT8
is required forin human cells1
1 study
KAT8
is required forin human cells1
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
Associations
1H4K16ac
downin human cells1
1 study
H4K16ac
downin human cells1
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