Global organization of replication time zones of the mouse genome

被引:125
作者
Farkash-Amar, Shlomit [1 ]
Lipson, Doron [2 ]
Polten, Andreas [3 ]
Goren, Alon [4 ]
Helmstetter, Charles [5 ]
Yakhini, Zohar [2 ,6 ]
Simon, Itamar [1 ]
机构
[1] Hebrew Univ Jerusalem, Sch Med, Dept Mol Biol, IL-91120 Jerusalem, Israel
[2] Technion Israel Inst Technol, Dept Comp Sci, IL-32000 Haifa, Israel
[3] Agilent Technol, D-76337 Waldbronn, Germany
[4] Hebrew Univ Jerusalem, Sch Med, Dept Cellular Biochem & Human Genet, IL-91120 Jerusalem, Israel
[5] Florida Inst Technol, Dept Biol Sci, Melbourne, FL 32901 USA
[6] Agilent Technol, IL-49527 Tel Aviv, Israel
基金
以色列科学基金会;
关键词
D O I
10.1101/gr.079566.108
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
The division of genomes into distinct replication time zones has long been established. However, an in-depth understanding of their organization and their relationship to transcription is incomplete. Taking advantage of a novel synchronization method ("baby machine") and of genomic DNA microarrays, we have, for the first time, mapped replication times of the entire mouse genome at a high temporal resolution. Our data revealed that although most of the genome has a distinct time of replication either early, middle, or late S phase, a significant portion of the genome is replicated asynchronously. Analysis of the replication map revealed the genomic scale organization of the replication time zones. We found that the genomic regions between early and late replication time zones often consist of extremely large replicons. Analysis of the relationship between replication and transcription revealed that early replication is frequently correlated with the transcription potential of a gene and not necessarily with its actual transcriptional activity. These findings, along with the strong conservation found between replication timing in human and mouse genomes, emphasize the importance of replication timing in transcription regulation.
引用
收藏
页码:1562 / 1570
页数:9
相关论文
共 56 条
[1]   Chromatin signatures of pluripotent cell lines [J].
Azuara, V ;
Perry, P ;
Sauer, S ;
Spivakov, M ;
Jorgensen, HF ;
John, RM ;
Gouti, M ;
Casanova, M ;
Warnes, G ;
Merkenschlager, M ;
Fisher, AG .
NATURE CELL BIOLOGY, 2006, 8 (05) :532-U189
[2]   Heritable gene silencing in lymphocytes delays chromatid resolution without affecting the timing of DNA replication [J].
Azuara, V ;
Brown, KE ;
Williams, RRE ;
Webb, N ;
Dillon, N ;
Festenstein, R ;
Buckle, V ;
Merkenschlager, M ;
Fisher, AG .
NATURE CELL BIOLOGY, 2003, 5 (07) :668-U49
[3]   Heterogeneity of eukaryotic replicons, replicon clusters, and replication foci [J].
Berezney, R ;
Dubey, DD ;
Huberman, JA .
CHROMOSOMA, 2000, 108 (08) :471-484
[4]   WHEN REPLICATION FORKS STOP [J].
BIERNE, H ;
MICHEL, B .
MOLECULAR MICROBIOLOGY, 1994, 13 (01) :17-23
[5]   THE TEMPORAL-ORDER OF REPLICATION OF MURINE IMMUNOGLOBULIN HEAVY-CHAIN CONSTANT REGION SEQUENCES CORRESPONDS TO THEIR LINEAR ORDER IN THE GENOME [J].
BRAUNSTEIN, JD ;
SCHULZE, D ;
DELGIUDICE, T ;
FURST, A ;
SCHILDKRAUT, CL .
NUCLEIC ACIDS RESEARCH, 1982, 10 (21) :6887-6902
[6]   Initiation of DNA replication at the human β-globin 3′ enhancer [J].
Buzina, A ;
Aladjem, MI ;
Kolman, JL ;
Wahl, GM ;
Ellis, J .
NUCLEIC ACIDS RESEARCH, 2005, 33 (14) :4412-4424
[7]   ALLELIC INACTIVATION REGULATES OLFACTORY RECEPTOR GENE-EXPRESSION [J].
CHESS, A ;
SIMON, I ;
CEDAR, H ;
AXEL, R .
CELL, 1994, 78 (05) :823-834
[8]  
DROUIN R, 1994, ADV HUM GENET, V22, P47
[9]   EUKARYOTIC CHROMOSOME REPLICATION [J].
EDENBERG, HJ ;
HUBERMAN, JA .
ANNUAL REVIEW OF GENETICS, 1975, 9 :245-284
[10]   Evidence that a single replication fork proceeds from early to late replicating domains in the IgH locus in a non-B cell line [J].
Ermakova, OV ;
Nguyen, LH ;
Little, RD ;
Chevillard, C ;
Riblet, R ;
Ashouian, N ;
Birshtein, BK ;
Schildkraut, CL .
MOLECULAR CELL, 1999, 3 (03) :321-330