Variant histone H2A.Z is globally localized to the promoters of inactive yeast genes and regulates nucleosome positioning

被引:334
作者
Guillemette, B
Bataille, AR
Gévry, N
Adam, M
Blanchette, M
Robert, F [1 ]
Gaudreau, L
机构
[1] Inst Rech Clin Montreal, Lab Chromatine & Express Genome, Montreal, PQ H2W 1R7, Canada
[2] Univ Sherbrooke, Fac Sci, Ctr Rech Mecanismes Fonctionnement Cellulaire, Dept Biol, Sherbrooke, PQ J1K 2R1, Canada
[3] McGill Ctr Bioinformat, Montreal, PQ, Canada
关键词
D O I
10.1371/journal.pbio.0030384
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
H2A.Z is an evolutionary conserved histone variant involved in transcriptional regulation, antisilencing, silencing, and genome stability. The mechanism(s) by which H2A.Z regulates these various biological functions remains poorly defined, in part due to the lack of knowledge regarding its physical location along chromosomes and the bearing it has in regulating chromatin structure. Here we mapped H2A.Z across the yeast genome at an approximately 300-bp resolution, using chromatin immunoprecipitation combined with tiling microarrays. We have identified 4,862 small regions-typically one or two nucleosomes wide-decorated with H2A.Z. Those "Z loci'' are predominantly found within specific nucleosomes in the promoter of inactive genes all across the genome. Furthermore, we have shown that H2A.Z can regulate nucleosome positioning at the GAL1 promoter. Within HZAD domains, the regions where H2A.Z shows an antisilencing function, H2A.Z is localized in a wider pattern, suggesting that the variant histone regulates a silencing and transcriptional activation via different mechanisms. Our data suggest that the incorporation of H2A.Z into specific promoter-bound nucleosomes configures chromatin structure to poise genes for transcriptional activation. The relevance of these findings to higher eukaryotes is discussed.
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收藏
页码:2100 / 2110
页数:11
相关论文
共 63 条
  • [1] Characterization of the stability and folding of H2A.Z chromatin particles -: Implications for transcriptional activation
    Abbott, DW
    Ivanova, VS
    Wang, XY
    Bonner, WM
    Ausió, J
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (45) : 41945 - 41949
  • [2] H2A.Z is required for global chromatin integrity and for recruitment of RNA polymerase II under specific conditions
    Adam, M
    Robert, F
    Larochelle, M
    Gaudreau, L
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (18) : 6270 - 6279
  • [3] HISTONE VARIANTS SPECIFIC TO THE TRANSCRIPTIONALLY ACTIVE, AMITOTICALLY DIVIDING MACRONUCLEUS OF THE UNICELLULAR EUCARYOTE, TETRAHYMENA-THERMOPHILA
    ALLIS, CD
    GLOVER, CVC
    BOWEN, JK
    GOROVSKY, MA
    [J]. CELL, 1980, 20 (03) : 609 - 617
  • [4] GAL4 DISRUPTS A REPRESSING NUCLEOSOME DURING ACTIVATION OF GAL1 TRANSCRIPTION INVIVO
    AXELROD, JD
    REAGAN, MS
    MAJORS, J
    [J]. GENES & DEVELOPMENT, 1993, 7 (05) : 857 - 869
  • [5] Removal of promoter nucleosomes by disassembly rather than sliding in vivo
    Boeger, H
    Griesenbeck, J
    Strattan, JS
    Kornberg, RD
    [J]. MOLECULAR CELL, 2004, 14 (05) : 667 - 673
  • [6] Nucleosomes unfold completely at a transcriptionally active promoter
    Boeger, H
    Griesenbeck, J
    Strattan, JS
    Kornberg, RD
    [J]. MOLECULAR CELL, 2003, 11 (06) : 1587 - 1598
  • [7] Regions of variant histone His2AvD required for Drosophila development
    Clarkson, MJ
    Wells, JRE
    Gibson, F
    Saint, R
    Tremethick, DJ
    [J]. NATURE, 1999, 399 (6737) : 694 - 697
  • [8] A histone variant, Htz1p, and a Sir1p-like protein, Esc2p, mediate silencing at HMR
    Dhillon, N
    Kamakaka, RT
    [J]. MOLECULAR CELL, 2000, 6 (04) : 769 - 780
  • [9] DROUIN S, 2005, IN PRESS METHODS
  • [10] Histone variant H2A.Z is required for early mammalian development
    Faast, R
    Thonglairoam, V
    Schulz, TC
    Beall, J
    Wells, JRE
    Taylor, H
    Matthaei, K
    Rathjen, PD
    Tremethick, DJ
    Lyons, I
    [J]. CURRENT BIOLOGY, 2001, 11 (15) : 1183 - 1187