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.
The c-myc insulator element and matrix attachment regions define the c-myc chromosomal domain.
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作者:Gombert Wendy M, Farris Stephen D, Rubio Eric D, Morey-Rosler Kristin M, Schubach William H, Krumm Anton
| 期刊: | Molecular and Cellular Biology | 影响因子: | 2.700 |
| 时间: | 2003 | 起止号: | 2003 Dec;23(24):9338-48 |
| doi: | 10.1128/MCB.23.24.9338-9348.2003 | ||
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