Coordinate Regulation of the Gel-forming Mucin Genes at Chromosome 11p15.5

被引:14
作者
Gosalia, Nehal [1 ,2 ]
Leir, Shih-Hsing [1 ,2 ]
Harris, Ann [1 ,2 ,3 ]
机构
[1] Northwestern Univ, Human Mol Genet Program, Childrens Mem Res Ctr, Feinberg Sch Med, Chicago, IL 60614 USA
[2] Northwestern Univ, Dept Pediat, Feinberg Sch Med, Chicago, IL 60614 USA
[3] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Feinberg Sch Med, Chicago, IL 60614 USA
基金
美国国家卫生研究院;
关键词
INSULATOR PROTEIN CTCF; DEVELOPMENTAL EXPRESSION; DNA METHYLATION; UP-REGULATION; CELL LINE; MUC5AC; IDENTIFICATION; ORGANIZATION; CARCINOMA; SEQUENCE;
D O I
10.1074/jbc.M112.437400
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
Four of the genes that encode gel-forming mucins, which are major components of the mucus layer protecting many epithelial surfaces, are clustered at chromosome 11p15.5 and show both cell-and tissue-specific expression patterns. We aimed to determine whether the individual genes were coordinately regulated by mechanisms involving higher order chromatin structure. CCCTC-binding factor (CTCF) sites were predicted in silico and CTCF occupancy then evaluated by chromatin immunoprecipitation. CTCF was found at many sites across the gene cluster, and its binding was correlated with mucin gene expression. Next, siRNA-mediated depletion of CTCF was shown to increase MUC2 expression in A549 lung carcinoma cells and both MUC6 and MUC5AC expression in LS180 colon carcinoma cells. These changes correlated with loss of CTCF binding at multiple sites, although others retained occupancy. In cells actively expressing the mucins, the gene cluster was shown by chromosome conformation capture to form looped three-dimensional structures with direct interactions between the MUC2 promoter region, regions 30 kb 5' to it, close to the MUC6 promoter and others near the 3' end of MUC5AC, >170 kb away. Finally, to demonstrate the importance of CTCF binding to mucin gene expression, Calu-3 lung carcinoma cells were exposed to lipopolysaccharide (LPS). LPS increased the expression of MUC2 and MUC5AC and reduced MUC5B. CTCF occupancy was concurrently depleted at specific binding sites close to these genes. These data suggest that CTCF binding and cell type-specific long-range interactions across the 11p15.5 gene cluster are critical mechanisms for coordinating gel-forming mucin gene expression.
引用
收藏
页码:6717 / 6725
页数:9
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