The temporal program of DNA replication: new insights into old questions

被引:52
作者
Zink, Daniele [1 ]
机构
[1] Univ Munich, Dept Biol 2, Biozentrum, D-82152 Martinsried, Germany
关键词
D O I
10.1007/s00412-006-0062-8
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
During the last decades it has been shown that the replication timing program in metazoans is related to chromosome structure, the nuclear positioning and AT/GC content of chromosomal loci, their patterns of histone modifications, and their transcriptional regulation. Here, the current state of knowledge concerning these relationships is reviewed. An integrated view on structure-function relationships in the nucleus is provided and the determination and functional role of the replication timing program is discussed in this context. A corresponding comprehensive model is developed and a key aspect of this model is the suggestion that mammalian chromosomes are organized into stable units equivalent to replicon clusters. It is proposed that the nuclear positions of these units would depend on their histone modifications and determine the replication timing of the whole unit. It is furthermore predicted that replication timing is only indirectly linked to transcriptional regulation and contributes to the maintenance of gene expression patterns. These clear predictions, and the fact that the tools are at hand now to further test them, open an avenue towards solving the long standing problem on how replication timing is determined in metazoan cells.
引用
收藏
页码:273 / 287
页数:15
相关论文
共 95 条
[1]   Replication labeling patterns and chromosome territories typical of mammalian nuclei are conserved in the early metazoan Hydra [J].
Alexandrova, O ;
Solovei, I ;
Cremer, T ;
David, CN .
CHROMOSOMA, 2003, 112 (04) :190-200
[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]  
Berezney R, 1995, INT REV CYTOL, V162A, P1
[5]  
BRANCO MR, 2006, IN PRESS PLOS BIOL
[6]   Expression of α- and β-globin genes occurs within different nuclear domains in haemopoietic cells [J].
Brown, KE ;
Amoils, S ;
Horn, JM ;
Buckle, VJ ;
Higgs, DR ;
Merkenschlager, M ;
Fisher, AG .
NATURE CELL BIOLOGY, 2001, 3 (06) :602-606
[7]  
CAMARGO M, 1982, AM J HUM GENET, V34, P757
[8]   The human transcriptome map:: Clustering of highly expressed genes in chromosomal domains [J].
Caron, H ;
van Schaik, B ;
van der Mee, M ;
Baas, F ;
Riggins, G ;
van Sluis, P ;
Hermus, MC ;
van Asperen, R ;
Boon, K ;
Voûte, PA ;
Heisterkamp, S ;
van Kampen, A ;
Versteeg, R .
SCIENCE, 2001, 291 (5507) :1289-+
[9]   Nuclear re-organisation of the Hoxb complex during mouse embryonic development [J].
Chambeyron, S ;
Da Silva, NR ;
Lawson, KA ;
Bickmore, WA .
DEVELOPMENT, 2005, 132 (09) :2215-2223
[10]   Chromatin decondensation and nuclear reorganization of the HoxB locus upon induction of transcription [J].
Chambeyron, S ;
Bickmore, WA .
GENES & DEVELOPMENT, 2004, 18 (10) :1119-1130