Sp1 and AP2 transcription factors are required for the human fragile mental retardation promoter activity in SK-N-SH neuronal cells

被引:14
作者
Carrillo, C [1 ]
Cisneros, B [1 ]
Montañez, C [1 ]
机构
[1] Inst Politecn Nacl, Ctr Invest & Estudios Avanzados, Dept Genet & Biol Mol, Mexico City 07000, DF, Mexico
关键词
fragile mental retardation promoter; promoter activity; Sp1; AP2;
D O I
10.1016/S0304-3940(99)00798-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The promoter of the human fragile mental retardation gene:(FMR1) was functionally analyzed in order to identify elements responsible for its regulation, Plasmids carrying the wild type or different deleted-promoter sequences driving the chloramphenicol acetyl transferase gene (CAT) were transiently transfected into the SK-N-SH cells and the CAT activity was assessed. Deletion studies suggested that major regulatory elements are present in a DNA region between positions -123 and -51. Gel mobility shift and footprinting assays using a DNA fragment encompassing that promoter region showed that SP1 and AP2 transcription factors could be involved in the functioning of the FMR1 promoter. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:149 / 152
页数:4
相关论文
共 22 条
  • [1] FMR1 PROTEIN - CONSERVED RNP FAMILY DOMAINS AND SELECTIVE RNA-BINDING
    ASHLEY, CT
    WILKINSON, KD
    REINES, D
    WARREN, ST
    [J]. SCIENCE, 1993, 262 (5133) : 563 - 566
  • [2] ENHANCED FMR-1 EXPRESSION IN TESTIS
    BACHNER, D
    STEINBACH, P
    WOHRLE, D
    JUST, W
    VOGEL, W
    HAMEISTER, H
    MANCA, A
    POUSTKA, A
    [J]. NATURE GENETICS, 1993, 4 (02) : 115 - 116
  • [3] REPORTER CONSTRUCTS WITH LOW BACKGROUND ACTIVITY UTILIZING THE CAT GENE
    BOSHART, M
    KLUPPEL, M
    SCHMIDT, A
    SCHUTZ, G
    LUCKOW, B
    [J]. GENE, 1992, 110 (01) : 129 - 130
  • [4] In vitro reactivation of the FMR1 gene involved in fragile X syndrome
    Chiurazzi, P
    Pomponi, MG
    Willemsen, R
    Oostra, BA
    Neri, G
    [J]. HUMAN MOLECULAR GENETICS, 1998, 7 (01) : 109 - 113
  • [5] THE FMR-1 PROTEIN IS CYTOPLASMIC, MOST ABUNDANT IN NEURONS AND APPEARS NORMAL IN CARRIERS OF A FRAGILE X PREMUTATION
    DEVYS, D
    LUTZ, Y
    ROUYER, N
    BELLOCQ, JP
    MANDEL, JL
    [J]. NATURE GENETICS, 1993, 4 (04) : 335 - 340
  • [6] Structural and functional characterization of the human FMR1 promoter reveals similarities with the hnRNP-A2 promoter region
    Drouin, R
    Angers, M
    Dallaire, N
    Rose, TM
    Khandjian, EW
    Rousseau, F
    [J]. HUMAN MOLECULAR GENETICS, 1997, 6 (12) : 2051 - 2060
  • [7] FINE-STRUCTURE OF THE HUMAN FMR1 GENE
    EICHLER, EE
    RICHARDS, S
    GIBBS, RA
    NELSON, DL
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (08) : 1147 - 1153
  • [8] VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX
    FU, YH
    KUHL, DPA
    PIZZUTI, A
    PIERETTI, M
    SUTCLIFFE, JS
    RICHARDS, S
    VERKERK, AJMH
    HOLDEN, JJA
    FENWICK, RG
    WARREN, ST
    OOSTRA, BA
    NELSON, DL
    CASKEY, CT
    [J]. CELL, 1991, 67 (06) : 1047 - 1058
  • [9] TISSUE SPECIFIC EXPRESSION OF FMR-1 PROVIDES EVIDENCE FOR A FUNCTIONAL-ROLE IN FRAGILE-X SYNDROME
    HINDS, HL
    ASHLEY, CT
    SUTCLIFFE, JS
    NELSON, DL
    WARREN, ST
    HOUSMAN, DE
    SCHALLING, M
    [J]. NATURE GENETICS, 1993, 3 (01) : 36 - 43
  • [10] INVITRO DNA METHYLATION INHIBITS FMR-1 PROMOTER
    HWU, WL
    LEE, YM
    LEE, SC
    WANG, TR
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 193 (01) : 324 - 329