Genome-wide localization of pre-RC sites and identification of replication origins in fission yeast

被引:134
作者
Hayashi, Makoto
Katou, Yuki
Itoh, Takehiko
Tazumi, Mitsutoshi
Yamada, Yoshiki
Takahashi, Tatsuro
Nakagawa, Takuro
Shirahige, Katsuhiko
Masukata, Hisao
机构
[1] Osaka Univ, Dept Biol, Grad Sch Sci, Toyonaka, Osaka 5600043, Japan
[2] Riken Genom Sci Ctr, Human Genome Res Grp, Genome Informat Team, Tsurumi Ku, Yokohama, Kanagawa, Japan
[3] Mitsubishi Res Inst Inc, Res Ctr Adv Sci & Technol, Chiyoda Ku, Tokyo, Japan
[4] Tokyo Inst Technol, Ctr Biol Resources & Informat, Div Gene Res, Midori Ku, Yokohama, Kanagawa 227, Japan
[5] Tokyo Inst Technol, Grad Sch Biosci & Biotechnol, Midori Ku, Yokohama, Kanagawa 227, Japan
关键词
centromere; DNA microarray; fission yeast; replication origin; subtelomere;
D O I
10.1038/sj.emboj.7601585
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA replication of eukaryotic chromosomes initiates at a number of discrete loci, called replication origins. Distribution and regulation of origins are important for complete duplication of the genome. Here, we determined locations of Orc1 and Mcm6, components of pre-replicative complex (pre-RC), on the whole genome of Schizosaccharomyces pombe using a high-resolution tiling array. Pre-RC sites were identified in 460 intergenic regions, where Orc1 and Mcm6 colocalized. By mapping of 5-bromo-2'-deoxyuridine (BrdU)-incorporated DNA in the presence of hydroxyurea (HU), 307 pre-RC sites were identified as earlyfiring origins. In contrast, 153 pre-RC sites without BrdU incorporation were considered to be late and/or inefficient origins. Inactivation of replication checkpoint by Cds1 deletion resulted in BrdU incorporation with HU specifically at the late origins. Early and late origins tend to distribute separately in large chromosome regions. Interestingly, pericentromeric heterochromatin and the silent mating-type locus replicated in the presence of HU, whereas the inner centromere or subtelomeric heterochromatin did not. Notably, MCM did not bind to inner centromeres where origin recognition complex was located. Thus, replication is differentially regulated in chromosome domains.
引用
收藏
页码:1327 / 1339
页数:13
相关论文
共 53 条
[1]   The Rpd3-Sin3 histone deacetylase regulates replication timing and enables intra-S origin control in Saccharomyces cerevisiae [J].
Aparicio, JG ;
Viggiani, CJ ;
Gibson, DG ;
Aparicio, OM .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (11) :4769-4780
[2]   A site- and strand-specific DNA break confers asymmetric switching potential in fission yeast [J].
Arcangioli, B .
EMBO JOURNAL, 1998, 17 (15) :4503-4510
[3]   DNA replication in eukaryotic cells [J].
Bell, SP ;
Dutta, A .
ANNUAL REVIEW OF BIOCHEMISTRY, 2002, 71 :333-374
[4]  
BICKMORE WA, 1995, J CELL SCI, V108, P2801
[5]   THE LOCALIZATION OF REPLICATION ORIGINS ON ARS PLASMIDS IN SACCHAROMYCES-CEREVISIAE [J].
BREWER, BJ ;
FANGMAN, WL .
CELL, 1987, 51 (03) :463-471
[6]   Comprehensive analysis of heterochromatin- and RNAi-mediated epigenetic control of the fission yeast genome [J].
Cam, HP ;
Sugiyama, T ;
Chen, ES ;
Chen, X ;
FitzGerald, PC ;
Grewal, SIS .
NATURE GENETICS, 2005, 37 (08) :809-819
[7]  
Chang YC, 2000, STAT MED, V19, P1277, DOI 10.1002/(SICI)1097-0258(20000530)19:10<1277::AID-SIM494>3.3.CO
[8]  
2-J
[9]   The fission yeast homologue of Orc4p binds to replication origin DNA via multiple AT-hooks [J].
Chuang, RY ;
Kelly, TJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) :2656-2661
[10]   Genetic analysis of an ARS element from the fission yeast Schizosaccharomyces pombe [J].
Clyne, RK ;
Kelly, TJ .
EMBO JOURNAL, 1995, 14 (24) :6348-6357