Thyroid hormone-regulated enhancer blocking: cooperation of CTCF and thyroid hormone receptor

被引:72
作者
Lutz, M
Burke, LJ
LeFevre, P
Myers, FA
Thorne, AW
Crane-Robinson, C
Bonifer, C
Filippova, GN
Lobanenkov, V
Renkawitz, R
机构
[1] Univ Giessen, Inst Genet, D-35392 Giessen, Germany
[2] Univ Leeds, St Jamess Univ Hosp, Mol Med Unit, Leeds LS9 7TF, W Yorkshire, England
[3] Univ Portsmouth, Fac Sci, Inst Biomed & Biomol Sci, Biophys Lab, Portsmouth PO1 2DT, Hants, England
[4] Fred Hutchinson Canc Res Ctr, Div Human Biol, Seattle, WA 98109 USA
[5] NIAID, Immunopathol Lab, NIH, Bethesda, MD 20892 USA
关键词
chromatin; CTCF; enhancer blocking; histone acetylation; thyroid hormone;
D O I
10.1093/emboj/cdg147
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
The highly conserved, ubiquitously expressed, zinc finger protein CTCF is involved in enhancer blocking, a mechanism crucial for shielding genes from illegitimate enhancer effects. Interestingly, CTCF-binding sites are often flanked by thyroid hormone response elements (TREs), as at the chicken lysozyme upstream silencer. Here we identify a similar composite site positioned upstream of the human c-myc gene. For both elements, we demonstrate that thyroid hormone abrogates enhancer blocking. Relief of enhancer blocking occurs even though CTCF remains bound to the lysozyme chromatin. Furthermore, chromatin immuno-precipitation analysis of the lysozyme upstream region revealed that histone H4 is acetylated at the CTCF-binding site. Loss of enhancer blocking by the addition of T3 led to increased histone acetylation, not only at the CTCF site, but also at the enhancer and the promoter. Thus, when TREs are adjacent to CTCF-binding sites, thyroid hormone can regulate enhancer blocking, thereby providing a new property for what was previously thought to be constitutive enhancer shielding by CTCF.
引用
收藏
页码:1579 / 1587
页数:9
相关论文
共 52 条
[1]   Nuclear hormone receptors and gene expression [J].
Aranda, A ;
Pascual, A .
PHYSIOLOGICAL REVIEWS, 2001, 81 (03) :1269-1304
[2]   DNA bending by the silencer protein NeP1 is modULATED BY TR and RXR [J].
Arnold, R ;
Burcin, M ;
Kaiser, B ;
Muller, M ;
Renkawitz, R ;
Rudiger, A .
NUCLEIC ACIDS RESEARCH, 1996, 24 (14) :2640-2647
[3]   Negative transcriptional regulation mediated by thyroid hormone response element 144 requires binding of the multivalent factor CTCF to a novel target DNA sequence [J].
Awad, TA ;
Bigler, J ;
Ulmer, JE ;
Hu, YJ ;
Moore, JM ;
Lutz, M ;
Neiman, PE ;
Collins, SJ ;
Renkawitz, R ;
Lobanenkov, VV ;
Filippova, GN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (38) :27092-27098
[4]   MODULAR STRUCTURE OF A CHICKEN LYSOZYME SILENCER - INVOLVEMENT OF AN UNUSUAL THYROID-HORMONE RECEPTOR-BINDING SITE [J].
BANIAHMAD, A ;
STEINER, C ;
KOHNE, AC ;
RENKAWITZ, R .
CELL, 1990, 61 (03) :505-514
[5]   Thyroid hormone negatively regulates the transcriptional activity of the β-amyloid precursor protein gene [J].
Belandia, B ;
Latasa, MJ ;
Villa, A ;
Pascual, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (46) :30366-30371
[6]   The protein CTCF is required for the enhancer blocking activity of vertebrate insulators [J].
Bell, AC ;
West, AG ;
Felsenfeld, G .
CELL, 1999, 98 (03) :387-396
[7]   Gene regulation - Insulators and boundaries: Versatile regulatory elements in the eukaryotic genome [J].
Bell, AC ;
West, AG ;
Felsenfeld, G .
SCIENCE, 2001, 291 (5503) :447-450
[8]   Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene [J].
Bell, AC ;
Felsenfeld, G .
NATURE, 2000, 405 (6785) :482-485
[9]   CHICKEN HEMATOPOIETIC-CELLS TRANSFORMED BY 7 STRAINS OF DEFECTIVE AVIAN LEUKEMIA VIRUSES DISPLAY 3 DISTINCT PHENOTYPES OF DIFFERENTIATION [J].
BEUG, H ;
VONKIRCHBACH, A ;
DODERLEIN, G ;
CONSCIENCE, JF ;
GRAF, T .
CELL, 1979, 18 (02) :375-390
[10]   NOVEL LOCATION AND FUNCTION OF A THYROID-HORMONE RESPONSE ELEMENT [J].
BIGLER, J ;
EISENMAN, RN .
EMBO JOURNAL, 1995, 14 (22) :5710-5723