Heterochromatin on the inactive X chromosome delays replication timing without affecting origin usage

被引:57
作者
Gómez, M [1 ]
Brockdorff, N [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Fac Med, MRC,Hammersmith Hosp, Ctr Clin Sci,X Inactivat Grp, London W12 0NN, England
关键词
D O I
10.1073/pnas.0401854101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
DNA replication origins (ORIs) map close to promoter regions in many organisms, including mammals. However, the relationship between initiation of replication and transcription is not well understood. To address this issue, we have analyzed replication timing and activity of several CpG island-associated ORIs on the transcriptionally active and silent X chromosomes. We find equivalent ORI usage and efficiency of both alleles at sites that are replicated late on the inactive X chromosome. Thus, in contrast to its repressive effect on transcription, heterochromatin does not influence ORI activity. These findings suggest that the relationship between sites of transcription and replication initiation at CpG island regions is restricted to early development, and that subsequent gene silencing and heterochromatin formation influence only the timing of ORI activation.
引用
收藏
页码:6923 / 6928
页数:6
相关论文
共 66 条
[1]   PARTICIPATION OF THE HUMAN BETA-GLOBIN LOCUS-CONTROL REGION IN INITIATION OF DNA-REPLICATION [J].
ALADJEM, MI ;
GROUDINE, M ;
BRODY, LL ;
DIEKEN, ES ;
FOURNIER, REK ;
WAHL, GM ;
EPNER, EM .
SCIENCE, 1995, 270 (5237) :815-819
[2]   NUMBER OF CPG ISLANDS AND GENES IN HUMAN AND MOUSE [J].
ANTEQUERA, F ;
BIRD, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11995-11999
[3]   CpG islands as genomic footprints of promoters that are associated with replication origins [J].
Antequera, F ;
Bird, A .
CURRENT BIOLOGY, 1999, 9 (17) :R661-R667
[4]   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
[5]   RNA polymerase II and III transcription factors can stimulate DNA replication by modifying origin chromatin structures [J].
Bodmer-Glavas, M ;
Edler, K ;
Barberis, A .
NUCLEIC ACIDS RESEARCH, 2001, 29 (22) :4570-4580
[6]   Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomes [J].
Boggs, BA ;
Cheung, P ;
Heard, E ;
Spector, DL ;
Chinault, AC ;
Allis, CD .
NATURE GENETICS, 2002, 30 (01) :73-76
[7]   DNA replication control through interaction of E2F-RB and the origin recognition complex [J].
Bosco, G ;
Du, W ;
Orr-Weaver, TL .
NATURE CELL BIOLOGY, 2001, 3 (03) :289-295
[8]   CONSERVATION OF POSITION AND EXCLUSIVE EXPRESSION OF MOUSE XIST FROM THE INACTIVE X-CHROMOSOME [J].
BROCKDORFF, N ;
ASHWORTH, A ;
KAY, GF ;
COOPER, P ;
SMITH, S ;
MCCABE, VM ;
NORRIS, DP ;
PENNY, GD ;
PATEL, D ;
RASTAN, S .
NATURE, 1991, 351 (6324) :329-331
[9]   Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene [J].
Carrel, L ;
Hunt, PA ;
Willard, HF .
HUMAN MOLECULAR GENETICS, 1996, 5 (09) :1361-1366
[10]   Long-distance control of origin choice and replication timing in the human β-globin locus are independent of the locus control region [J].
Cimbora, DM ;
Schübeler, D ;
Reik, A ;
Hamilton, J ;
Francastel, C ;
Epner, EM ;
Groudine, M .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (15) :5581-5591