BRPF3-HBO1 regulates replication origin activation and histone H3K14 acetylation
Research output: Contribution to journal › Journal article › Research › peer-review
Standard
BRPF3-HBO1 regulates replication origin activation and histone H3K14 acetylation. / Feng, Yunpeng; Vlassis, Arsenios; Roques, Céline; Lalonde, Marie Eve; Gonzalez Aguilera, Cristina; Lambert, Jean Philippe; Lee, Sung-Bau; Zhao, Xiaobei; Alabert, Constance; Johansen, Jens Vilstrup; Paquet, Eric; Yang, Xiang Jiao; Gingras, Anne Claude; Côté, Jacques; Groth, Anja.
In: EMBO Journal, Vol. 35, No. 2, 2016, p. 176-192.Research output: Contribution to journal › Journal article › Research › peer-review
Harvard
APA
Vancouver
Author
Bibtex
}
RIS
TY - JOUR
T1 - BRPF3-HBO1 regulates replication origin activation and histone H3K14 acetylation
AU - Feng, Yunpeng
AU - Vlassis, Arsenios
AU - Roques, Céline
AU - Lalonde, Marie Eve
AU - Gonzalez Aguilera, Cristina
AU - Lambert, Jean Philippe
AU - Lee, Sung-Bau
AU - Zhao, Xiaobei
AU - Alabert, Constance
AU - Johansen, Jens Vilstrup
AU - Paquet, Eric
AU - Yang, Xiang Jiao
AU - Gingras, Anne Claude
AU - Côté, Jacques
AU - Groth, Anja
PY - 2016
Y1 - 2016
N2 - During DNA replication, thousands of replication origins are activated across the genome. Chromatin architecture contributes to origin specification and usage, yet it remains unclear which chromatin features impact on DNA replication. Here, we perform a RNAi screen for chromatin regulators implicated in replication control by measuring RPA accumulation upon replication stress. We identify six factors required for normal rates of DNA replication and characterize a function of the bromodomain and PHD finger-containing protein 3 (BRPF3) in replication initiation. BRPF3 forms a complex with HBO1 that specifically acetylates histone H3K14, and genomewide analysis shows high enrichment of BRPF3, HBO1 and H3K14ac at ORC1-binding sites and replication origins found in the vicinity of TSSs. Consistent with this, BRPF3 is necessary for H3K14ac at selected origins and efficient origin activation. CDC45 recruitment, but not MCM2-7 loading, is impaired in BRPF3-depleted cells, identifying a BRPF3-dependent function of HBO1 in origin activation that is complementary to its role in licencing. We thus propose that BRPF3-HBO1 acetylation of histone H3K14 around TSS facilitates efficient activation of nearby replication origins.
AB - During DNA replication, thousands of replication origins are activated across the genome. Chromatin architecture contributes to origin specification and usage, yet it remains unclear which chromatin features impact on DNA replication. Here, we perform a RNAi screen for chromatin regulators implicated in replication control by measuring RPA accumulation upon replication stress. We identify six factors required for normal rates of DNA replication and characterize a function of the bromodomain and PHD finger-containing protein 3 (BRPF3) in replication initiation. BRPF3 forms a complex with HBO1 that specifically acetylates histone H3K14, and genomewide analysis shows high enrichment of BRPF3, HBO1 and H3K14ac at ORC1-binding sites and replication origins found in the vicinity of TSSs. Consistent with this, BRPF3 is necessary for H3K14ac at selected origins and efficient origin activation. CDC45 recruitment, but not MCM2-7 loading, is impaired in BRPF3-depleted cells, identifying a BRPF3-dependent function of HBO1 in origin activation that is complementary to its role in licencing. We thus propose that BRPF3-HBO1 acetylation of histone H3K14 around TSS facilitates efficient activation of nearby replication origins.
KW - BRPF
KW - DNA replication
KW - H3K14ac
KW - HBO1
KW - Origin activation
U2 - 10.15252/embj.201591293
DO - 10.15252/embj.201591293
M3 - Journal article
C2 - 26620551
VL - 35
SP - 176
EP - 192
JO - E M B O Journal
JF - E M B O Journal
SN - 0261-4189
IS - 2
ER -
ID: 153413621