Transcriptional activation by bidirectional RNA polymerase II elongation over a silent promoter

被引:12
作者
Leupin, O
Attanasio, C
Marguerat, S
Tapernoux, M
Antonarakis, SE
Conrad, B
机构
[1] Univ Geneva, Sch Med, CMU, Dept Genet Med & Dev, CH-1211 Geneva, Switzerland
[2] Univ Geneva, Sch Med, CMU, Dept Genet & Microbiol, CH-1211 Geneva, Switzerland
关键词
transcriptional interference; human LTR transposons; RNA polymerase II; Pol II-regulated transcription; transcriptome diversity;
D O I
10.1038/sj.embor.7400502
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
Transcriptional interference denotes negative cis effects between promoters. Here, we show that promoters can also interact positively. Bidirectional RNA polymerase II (Pol II) elongation over the silent human endogenous retrovirus ( HERV)-K18 promoter ( representative of 2.5 +/- 10(3) similar promoters genome-wide) activates transcription. In tandem constructs, an upstream promoter activates HERV-K18 transcription. This is abolished by inversion of the upstream promoter, or by insertion of a poly( A) signal between the promoters; transcription is restored by poly( A) signal mutants. TATA-box mutants in the upstream promoter reduce HERV-K18 transcription. Experiments with the same promoters in a convergent orientation produce similar effects. A small promoter deletion partially restores HERV-K18 activity, consistent with activation resulting from repressor repulsion by the elongating Pol II. Transcriptional elongation over this class of intragenic promoters will generate co-regulated sense - antisense transcripts, or, alternatively initiating transcripts, thus expanding the diversity and complexity of the human transcriptome.
引用
收藏
页码:956 / 960
页数:5
相关论文
共 30 条
  • [1] PROMOTER OCCLUSION - TRANSCRIPTION THROUGH A PROMOTER MAY INHIBIT ITS ACTIVITY
    ADHYA, S
    GOTTESMAN, M
    [J]. CELL, 1982, 29 (03) : 939 - 944
  • [2] Many human endogenous retrovirus K (HERV-K) proviruses are unique to humans
    Barbulescu, M
    Turner, G
    Seaman, MI
    Deinard, AS
    Kidd, KK
    Lenz, J
    [J]. CURRENT BIOLOGY, 1999, 9 (16) : 861 - 868
  • [3] COMPLEX REGULATION OF SIMIAN VIRUS-40 EARLY-REGION TRANSCRIPTION FROM DIFFERENT OVERLAPPING PROMOTERS
    BUCHMAN, AR
    FROMM, M
    BERG, P
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1984, 4 (09) : 1900 - 1914
  • [4] Transcriptional interference between convergent promoters caused by elongation over the promoter
    Callen, BP
    Shearwin, KE
    Egan, JB
    [J]. MOLECULAR CELL, 2004, 14 (05) : 647 - 656
  • [5] Coding defect and a TATA box mutation at the bilirubin UDP-glucuronosyltransferase gene cause Crigler-Najjar type I disease
    Ciotti, M
    Chen, F
    Rubaltelli, FF
    Owens, IS
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1998, 1407 (01): : 40 - 50
  • [6] Solitary HERV-K LTRs possess bi-directional promoter activity and contain a negative regulatory element in the U5 region
    Domansky, AN
    Kopantzev, EP
    Snezhkov, EV
    Lebedev, YB
    Leib-Mosch, C
    Sverdlov, ED
    [J]. FEBS LETTERS, 2000, 472 (2-3) : 191 - 195
  • [7] POSITION AND DENSITY EFFECTS ON REPRESSION BY STATIONARY AND MOBILE DNA-BINDING PROTEINS
    ELLEDGE, SJ
    DAVIS, RW
    [J]. GENES & DEVELOPMENT, 1989, 3 (02) : 185 - 197
  • [8] Transcription through the roadblocks:: the role of RNA polymerase cooperation
    Epshtein, V
    Toulmé, F
    Rahmouni, AR
    Borukhov, S
    Nudler, E
    [J]. EMBO JOURNAL, 2003, 22 (18) : 4719 - 4727
  • [9] Transcriptional interference perturbs the binding of Sp1 to the HIV-1 promoter
    Greger, IH
    Demarchi, F
    Giacca, M
    Proudfoot, NJ
    [J]. NUCLEIC ACIDS RESEARCH, 1998, 26 (05) : 1294 - 1300
  • [10] Novel RNAs identified from an in-depth analysis of the transcriptome of human chromosomes 21 and 22
    Kampa, D
    Cheng, J
    Kapranov, P
    Yamanaka, M
    Brubaker, S
    Cawley, S
    Drenkow, J
    Piccolboni, A
    Bekiranov, S
    Helt, G
    Tammana, H
    Gingeras, TR
    [J]. GENOME RESEARCH, 2004, 14 (03) : 331 - 342