Methyl-CpG binding proteins identify novel sites of epigenetic inactivation in human cancer

被引:247
作者
Ballestar, E
Paz, MF
Valle, L
Wei, S
Fraga, MF
Espada, J
Cigudosa, JC
Huang, THM
Esteller, M
机构
[1] Spanish Natl Canc Ctr, Mol Pathol Programme, Epigenet Lab, Madrid 28029, Spain
[2] Spanish Natl Canc Ctr, Biotechnol Programme, Cytogenet Unit, Madrid, Spain
[3] Univ Missouri, Sch Med, Ellis Fischel Canc Ctr, Dept Pathol & Anat Sci, Columbia, MO 65203 USA
关键词
ChIP on chip; DNA methylation; epigenetic inactivation; MBD; MeCP2;
D O I
10.1093/emboj/cdg604
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
Methyl-CpG binding proteins (MBDs) mediate histone deacetylase-dependent transcriptional silencing at methylated CpG islands. Using chromatin immunoprecitation (ChIP) we have found that gene-specific profiles of MBDs exist for hypermethylated promoters of breast cancer cells, whilst a common pattern of histone modifications is shared. This unique distribution of MBDs is also characterized in chromosomes by comparative genomic hybridization of immunoprecipitated DNA and immunolocalization. Most importantly, we demonstrate that MBD association to methylated DNA serves to identify novel targets of epigenetic inactivation in human cancer. We combined the ChIP assay of MBDs with a CpG island microarray (ChIP on chip). The scenario revealed shows that, while many genes are regulated by multiple MBDs, others are associated with a single MBD. These target genes displayed methylation- associated transcriptional silencing in breast cancer cells and primary tumours. The candidates include the homeobox gene PAX6, the prolactin hormone receptor, and dipeptidylpeptidase IV among others. Our results support an essential role for MBDs in gene silencing and, when combined with genomic strategies, their potential to 'catch' new hypermethylated genes in cancer.
引用
收藏
页码:6335 / 6345
页数:11
相关论文
共 44 条
  • [1] Methyl-CpG binding domain protein 2 represses transcription from hypermethylated π-class glutathione S-transferase gene promoters in hepatocellular carcinoma cells
    Bakker, J
    Lin, XH
    Nelson, WG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (25) : 22573 - 22580
  • [2] Methyl-CpG-binding proteins - Targeting specific gene repression
    Ballestar, E
    Wolffe, AP
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 2001, 268 (01): : 1 - 6
  • [3] Prolactin as an autocrine/paracrine growth factor in human cancer
    Ben-Jonathan, N
    Liby, K
    McFarland, M
    Zinger, M
    [J]. TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2002, 13 (06) : 245 - 250
  • [4] Methylation-induced repression - Belts, braces, and chromatin
    Bird, AP
    Wolffe, AP
    [J]. CELL, 1999, 99 (05) : 451 - 454
  • [5] DNA METHYLATION AND GENE ACTIVITY
    CEDAR, H
    [J]. CELL, 1988, 53 (01) : 3 - 4
  • [6] G-protein-coupled receptor activation induces the membrane translocation and activation of phosphatidylinositol-4-phosphate 5-kinase Iα by a Rac- and Rho-dependent pathway
    Chatah, NEH
    Abrams, CS
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (36) : 34059 - 34065
  • [7] Heterozygous disruption of Hic1 predisposes mice to a gender-dependent spectrum of malignant tumors
    Chen, WY
    Zeng, XB
    Carter, MG
    Morrell, CN
    Yen, RWC
    Esteller, M
    Watkins, DN
    Herman, JG
    Mankowski, JL
    Baylin, SB
    [J]. NATURE GENETICS, 2003, 33 (02) : 197 - 202
  • [8] Characterization of nonrandom chromosomal gains and losses in multiple myeloma by comparative genomic hybridization
    Cigudosa, JC
    Rao, PH
    Calasanz, MJ
    Odero, MD
    Michaeli, J
    Jhanwar, SC
    Chaganti, RSK
    [J]. BLOOD, 1998, 91 (08) : 3007 - 3010
  • [9] DNA methylation analysis in mammalian cells
    Clark, SJ
    Warnecke, P
    [J]. METHODS, 2002, 27 (02) : 99 - 100
  • [10] Precipitous release of methyl-CpG binding protein 2 and histone deacetylase 1 from the methylated human multidrug resistance gene (MDR1) on activation
    El-Osta, A
    Kantharidis, P
    Zalcberg, JR
    Wolffe, AP
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (06) : 1844 - 1857