TY - JOUR
T1 - The replication timing program in the hands of two HDACs
AU - Yoshida, Kazumasa
AU - Lengronne, Armelle
AU - Pasero, Philippe
N1 - Funding Information:
Work in the Pasero laboratory is supported by the ‘Agence Nationale pour la Recherche’ (ANR), the ‘Institut National du Cancer’ (INCa) and the ‘Ligue contre le Cancer (équipe labellisée)’. KY was a fellow of the ‘Ligue contre le Cancer’.
Publisher Copyright:
© 2014 Yoshida et al.
PY - 2014/8
Y1 - 2014/8
N2 - In eukaryotes, duplication of genomic information depends on the sequential activation of multiple replication origins distributed along the chromosomes. Replication origins differ in initiation time, chromatin structure and three-dimensional position in the nucleus. Recently, we have performed a systematic analysis of the role of histone deacetylases (HDACs) in the regulation of origin activity in budding yeast. We have found that the epigenetic regulation of repetitive sequences is a key determinant of the DNA replication program. Indeed, our study revealed that two histone deacetylases, Rpd3 and Sir2, have opposite effects on the replication timing program. Rpd3 delays initiation at late origins, whereas Sir2 promotes efficient activation of early origins. Remarkably, we also found that Rpd3 and Sir2 regulate initiation at ~200 replication origins located within the ribosomal DNA (rDNA) array. We propose that this epigenetic regulation of repetitive origins controls the replication timing program by modulating the availability of limiting initiation factors.
AB - In eukaryotes, duplication of genomic information depends on the sequential activation of multiple replication origins distributed along the chromosomes. Replication origins differ in initiation time, chromatin structure and three-dimensional position in the nucleus. Recently, we have performed a systematic analysis of the role of histone deacetylases (HDACs) in the regulation of origin activity in budding yeast. We have found that the epigenetic regulation of repetitive sequences is a key determinant of the DNA replication program. Indeed, our study revealed that two histone deacetylases, Rpd3 and Sir2, have opposite effects on the replication timing program. Rpd3 delays initiation at late origins, whereas Sir2 promotes efficient activation of early origins. Remarkably, we also found that Rpd3 and Sir2 regulate initiation at ~200 replication origins located within the ribosomal DNA (rDNA) array. We propose that this epigenetic regulation of repetitive origins controls the replication timing program by modulating the availability of limiting initiation factors.
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U2 - 10.15698/mic2014.08.163
DO - 10.15698/mic2014.08.163
M3 - Review article
AN - SCOPUS:85013419644
SN - 2311-2638
VL - 1
SP - 273
EP - 275
JO - Microbial Cell
JF - Microbial Cell
IS - 8
ER -