TTF-I determines the chromatin architecture of the active rDNA promoter

被引:75
作者
Längst, G
Becker, PB
Grummt, I
机构
[1] Deutsch Krebsforschungszentrum, Div Mol Biol Cell 2, D-69120 Heidelberg, Germany
[2] European Mol Biol Lab, D-69117 Heidelberg, Germany
关键词
chromatin; nucleosome remodeling; RNA polymerase I; transcription activation; TTF-I;
D O I
10.1093/emboj/17.11.3135
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
Transcription of ribosomal genes assembled into chromatin requires binding of the transcription termination factor TTF-I to the promoter-proximal terminator To, To analyze the mechanism of TTF-I-mediated transcriptional activation, we have used mutant templates with altered sequence, polarity and distance of To with respect to the transcription start site, Transcription activation by TTF-I is chromatin specific and requires the precise positioning of the terminator relative to the promoter, Whereas termination by TTF-I depends on the correct orientation of a terminator, TTF-I-mediated transcriptional activation is orientation independent. TTF-I can bind to nucleosomal DNA in the absence of enzymatic activities that destabilize nucleosome structure. Chromatin-bound TTF-I synergizes with ATP-dependent cofactors present in extracts of Drosophila embryos and mouse cells to position a nucleosome over the rDNA promoter and the transcription start site. Nucleosome positioning correlates tightly with the activation of rDNA transcription. We suggest that transcriptional activation by TTF-I is a stepwise process involving the creation of a defined promoter architecture and that the positioning of a nucleosome is compatible with, if not a prerequisite for, transcription initiation from rDNA chromatin.
引用
收藏
页码:3135 / 3145
页数:11
相关论文
共 59 条
  • [11] A YEAST PROTEIN THAT INFLUENCES THE CHROMATIN STRUCTURE OF UASG AND FUNCTIONS AS A POWERFUL AUXILIARY GENE ACTIVATOR
    CHASMAN, DI
    LUE, NF
    BUCHMAN, AR
    LAPOINTE, JW
    LORCH, Y
    KORNBERG, RD
    [J]. GENES & DEVELOPMENT, 1990, 4 (04) : 503 - 514
  • [12] SUPERHELICAL STRESS AND NUCLEOSOME-MEDIATED REPRESSION OF 5S RNA GENE-TRANSCRIPTION INVITRO
    CLARK, DJ
    WOLFFE, AP
    [J]. EMBO JOURNAL, 1991, 10 (11) : 3419 - 3428
  • [13] LOCATION OF THE PRIMARY SITES OF MICROCOCCAL NUCLEASE CLEAVAGE ON THE NUCLEOSOME CORE
    COCKELL, M
    RHODES, D
    KLUG, A
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1983, 170 (02) : 423 - 446
  • [14] DIFFERENT DOMAINS OF THE MURINE RNA-POLYMERASE I-SPECIFIC TERMINATION FACTOR MTTF-I SERVE DISTINCT FUNCTIONS IN TRANSCRIPTION TERMINATION
    EVERS, R
    SMID, A
    RUDLOFF, U
    LOTTSPEICH, F
    GRUMMT, I
    [J]. EMBO JOURNAL, 1995, 14 (06) : 1248 - 1256
  • [15] Chromatin unfolds
    Felsenfeld, G
    [J]. CELL, 1996, 86 (01) : 13 - 19
  • [16] TRANSCRIPTION FACTOR REQUIREMENTS FOR INVITRO FORMATION OF TRANSCRIPTIONALLY COMPETENT 5S RIBOSOMAL-RNA GENE CHROMATIN
    FELTS, SJ
    WEIL, PA
    CHALKLEY, R
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (05) : 2390 - 2401
  • [17] NUCLEOSOME POSITIONING ON THE MMTV LTR RESULTS FROM THE FREQUENCY-BIASED OCCUPANCY OF MULTIPLE FRAMES
    FRAGOSO, G
    JOHN, S
    ROBERTS, MS
    HAGER, GL
    [J]. GENES & DEVELOPMENT, 1995, 9 (15) : 1933 - 1947
  • [18] Termination of mammalian rDNA replication: Polar arrest of replication fork movement by transcription termination factor TTF-I
    Gerber, JK
    Gogel, E
    Berger, C
    Wallisch, M
    Muller, F
    Grummt, I
    Grummt, F
    [J]. CELL, 1997, 90 (03) : 559 - 567
  • [19] TRANSCRIPTION OF MOUSE RDNA TERMINATES DOWNSTREAM OF THE 3' END OF 28S RNA AND INVOLVES INTERACTION OF FACTORS WITH REPEATED SEQUENCES IN THE 3' SPACER
    GRUMMT, I
    MAIER, U
    OHRLEIN, A
    HASSOUNA, N
    BACHELLERIE, JP
    [J]. CELL, 1985, 43 (03) : 801 - 810
  • [20] A REPEATED 18-BP SEQUENCE MOTIF IN THE MOUSE RDNA SPACER MEDIATES BINDING OF A NUCLEAR FACTOR AND TRANSCRIPTION TERMINATION
    GRUMMT, I
    ROSENBAUER, H
    NIEDERMEYER, I
    MAIER, U
    OHRLEIN, A
    [J]. CELL, 1986, 45 (06) : 837 - 846