The c-myc insulator element and matrix attachment regions define the c-myc chromosomal domain

被引:67
作者
Gombert, WM
Farris, SD
Rubio, ED
Morey-Rosler, KM
Schubach, WH
Krumm, A
机构
[1] Univ Washington, Sch Med, Dept Radiat Oncol, Seattle, WA 98104 USA
[2] Vet Adm Puget Sound Hlth Care Syst, Dept Med, Div Med Oncol, Seattle Div, Seattle, WA 98108 USA
关键词
D O I
10.1128/MCB.23.24.9338-9348.2003
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
Insulator elements and matrix attachment regions are essential for the organization of genetic information within the nucleus. By comparing the pattern of histone modifications at the mouse and human c-myc alleles, we identified an evolutionarily conserved boundary at which the c-myc transcription unit is separated from the flanking condensed chromatin enriched in lysine 9-methylated histone H3. This region harbors the c-myc insulator element (MINE), which contains at least two physically separable, functional activities: enhancer-blocking activity and barrier activity. The enhancer-blocking activity is mediated by CTCF. Chromatin immunoprecipitation assays demonstrate that CTCF is constitutively bound at the insulator and at the promoter region independent of the transcriptional status of c-myc. This result supports an architectural role of CTCF rather than a regulatory role in transcription. An additional higher-order nuclear organization of the c-myc locus is provided by matrix attachment regions (MARs) that define a domain larger than 160 kb. The MARs of the c-myc domain do not act to prevent the association of flanking regions with lysine 9-methylated histones, suggesting that they do not function as barrier elements.
引用
收藏
页码:9338 / 9348
页数:11
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