A 330 kb CENP-A binding domain and altered replication timing at a human neocentromere

被引:109
作者
Lo, AWI [1 ]
Craig, JM [1 ]
Saffery, R [1 ]
Kalitsis, P [1 ]
Irvine, DV [1 ]
Earle, E [1 ]
Magliano, DJ [1 ]
Choo, KHA [1 ]
机构
[1] Royal Childrens Hosp, Murdoch Childrens Res Inst, Melbourne, Vic 3052, Australia
关键词
CENP-A; centromere; chromatin; neocentromere; replication timing;
D O I
10.1093/emboj/20.8.2087
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
Centromere protein A (CENP-A) is an essential centromere-specific histone H3 homologue, Using combined chromatin immunoprecipitation and DNA array analysis, we have defined a 330 kb CENP-A binding domain of a 10q25.3 neocentromere found on the human marker chromosome mardel (10), This domain is situated adjacent to the 80 kb region identified previously as the neocentromere site through lower-resolution immunofluorescence/FISH analysis of metaphase chromosomes. The 330 kb CENP-A binding domain shows a depletion of histone H3, providing evidence for the replacement of histone H3 by CENP-A within centromere-specific nucleosomes. The DNA within this domain has a high AT-content comparable to that of alpha -satellite, a high prevalence of LINEs and tandem repeats, and fewer SINEs and potential genes than the surrounding region. FISH analysis indicates that the normal 10q25.3 genomic region replicates around mid-S phase, Neoceutromere formation is accompanied by a replication time lag around but not within the CENP-A binding region, with this lag being significantly more prominent to one side. The availability of fully sequenced genomic markers makes human neocentromeres a powerful model for dissecting the functional domains of complex higher eukaryotic centromeres.
引用
收藏
页码:2087 / 2096
页数:10
相关论文
共 59 条
  • [1] Aagaard L, 2000, J CELL SCI, V113, P817
  • [2] The 10q25 neocentromere and its inactive progenitor have identical primary nucleotide sequence: Further evidence for epigenetic modification
    Barry, AE
    Bateman, M
    Howman, EV
    Cancilla, MR
    Tainton, KM
    Irvine, DV
    Saffery, R
    Choo, KHA
    [J]. GENOME RESEARCH, 2000, 10 (06) : 832 - 838
  • [3] Sequence analysis of an 80 kb human neocentromere
    Barry, AE
    Howman, EV
    Cancilla, MR
    Saffery, R
    Choo, KHA
    [J]. HUMAN MOLECULAR GENETICS, 1999, 8 (02) : 217 - 227
  • [4] The human genome: Organization and evolutionary history
    Bernardi, G
    [J]. ANNUAL REVIEW OF GENETICS, 1995, 29 : 445 - 476
  • [5] BICKMORE WA, 1995, J CELL SCI, V108, P2801
  • [6] Analysis of DNA replication by fluorescence in situ hybridization
    Boggs, BA
    Chinault, AC
    [J]. METHODS-A COMPANION TO METHODS IN ENZYMOLOGY, 1997, 13 (03): : 259 - 270
  • [7] CAMARGO M, 1982, AM J HUM GENET, V34, P757
  • [8] Direct cloning of human 10q25 neocentromere DNA using transformation-associated recombination (TAR) in yeast
    Cancilla, MR
    Tainton, KM
    Barry, AE
    Larionov, V
    Kouprina, N
    Resnick, MA
    Du Sart, D
    Choo, KHA
    [J]. GENOMICS, 1998, 47 (03) : 399 - 404
  • [9] The N terminus of the centromere H3-like protein Cse4p performs an essential function distinct from that of the histone fold domain
    Chen, YH
    Baker, RE
    Keith, KC
    Harris, K
    Stoler, S
    Fitzgerald-Hayes, M
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (18) : 7037 - 7048
  • [10] Centromerization
    Choo, KHA
    [J]. TRENDS IN CELL BIOLOGY, 2000, 10 (05) : 182 - 188