Chromatin inheritance upon Zeste-mediated Brahma recruitment at a minimal cellular memory module

被引:72
作者
Déjardin, J [1 ]
Cavalli, G [1 ]
机构
[1] CNRS, Inst Human Genet, F-34396 Montpellier 5, France
关键词
cellular memory; chromatin; Polycomb group; trithorax group; Zeste;
D O I
10.1038/sj.emboj.7600108
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
Polycomb group and trithorax group proteins maintain the memory of repressed and active chromatin states by regulating chromatin of their target genes via DNA sequences termed Polycomb- and trithorax. response elements. Since these elements often overlap and are able to convey the memory of both silent and active chromatin through cell division, they were also defined as cellular memory modules (CMMs). We identify here a minimal CMM of 219 bp from the Drosophila Fab-7 region that regulates the homeotic gene Abdominal-B. This CMM conveys the inheritance of active chromatin states induced by an embryonic pulse of transcriptional activation via recruitment of the trithorax group proteins Trithorax (TRX) and Brahma (BRM) the Drosophila homologue of the SW12/SNF2 ATPase involved in chromatin remodelling. Within this CMM, DNA-binding sites for the Zeste protein are necessary for the inheritance of active chromatin through Zeste-dependent recruitment of BRM, while TRX can bind the CMM even in their absence. Thus, epigenetic inheritance of active chromatin states involves the recruitment of multiple cooperative chromatin-modifying complexes at closely spaced but distinct sites within a CMM.
引用
收藏
页码:857 / 868
页数:12
相关论文
共 58 条
  • [1] Americo J, 2002, GENETICS, V160, P1561
  • [2] The Drosophila BRM complex facilitates global transcription by RNA polymerase II
    Armstrong, JA
    Papoulas, O
    Daubresse, G
    Sperling, AS
    Lis, JT
    Scott, MP
    Tamkun, JW
    [J]. EMBO JOURNAL, 2002, 21 (19) : 5245 - 5254
  • [3] Inheritance of Polycomb-dependent chromosomal interactions in Drosophila
    Bantignies, F
    Grimaud, C
    Lavrov, S
    Gabut, M
    Cavalli, G
    [J]. GENES & DEVELOPMENT, 2003, 17 (19) : 2406 - 2420
  • [4] Functional interaction between the coactivator Drosophila CREB-binding protein and ASH1, a member of the trithorax group of chromatin modifiers
    Bantignies, F
    Goodman, RH
    Smolik, SM
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (24) : 9317 - 9330
  • [5] RETRACTED: Histone methylation by the Drosophila epigenetic transcriptional regulator Ash1 (Retracted article. See vol. 521, pg. 110, 2015)
    Beisel, C
    Imhof, A
    Greene, J
    Kremmer, E
    Sauer, F
    [J]. NATURE, 2002, 419 (6909) : 857 - 862
  • [6] THE DROSOPHILA-ZESTE PROTEIN BINDS COOPERATIVELY TO SITES IN MANY GENE REGULATORY REGIONS - IMPLICATIONS FOR TRANSVECTION AND GENE-REGULATION
    BENSON, M
    PIRROTTA, V
    [J]. EMBO JOURNAL, 1988, 7 (12) : 3907 - 3915
  • [7] ZESTE ENCODES A SEQUENCE-SPECIFIC TRANSCRIPTION FACTOR THAT ACTIVATES THE ULTRABITHORAX PROMOTER INVITRO
    BIGGIN, MD
    BICKEL, S
    BENSON, M
    PIRROTTA, V
    TJIAN, R
    [J]. CELL, 1988, 53 (05) : 713 - 722
  • [8] TRANSCRIPTION FACTORS THAT ACTIVATE THE ULTRABITHORAX PROMOTER IN DEVELOPMENTALLY STAGED EXTRACTS
    BIGGIN, MD
    TJIAN, R
    [J]. CELL, 1988, 53 (05) : 699 - 711
  • [9] Identification and characterization of polyhomeotic PREs and TREs
    Bloyer, S
    Cavalli, G
    Brock, HW
    Dura, JM
    [J]. DEVELOPMENTAL BIOLOGY, 2003, 261 (02) : 426 - 442
  • [10] ECTOPIC EXPRESSION IN DROSOPHILA
    BRAND, AH
    MANOUKIAN, AS
    PERRIMON, N
    [J]. METHODS IN CELL BIOLOGY, VOL 44, 1994, 44 : 635 - 654