TY - JOUR
T1 - Differential sensitivity of zinc finger transcription factors MTF-1, Sp1 and krox-20 to CpG methylation of their binding sites
AU - Radtke, Freddy
AU - Hug, Martin
AU - Georgiev, Oleg
AU - Matsuo, Koichi
AU - Schaffner, Walter
PY - 1996
Y1 - 1996
N2 - Cytosine methylation at CpG sites is often negatively correlated with mammalian gene activity. Many transcription factors whose DNA binding site contains one or more CpG dinucleotides are no longer able to efficiently bind DNA when the site is methylated. A notable exception is the zinc finger factor Sp1 which binds DNA and activates transcription even when its binding site is methylated. Here we show that two other zinc finger factors, MTF-1 and Krox-20, can also bind to CPG methylated sites. MTF-1 regulates metallothionein gene transcription by binding to a number of metal responsive elements (MREs), and Krox-20 regulates Hox genes during hindbrain segmentation. However, a refined analysis of MTF-1/MRE binding shows that methylation is not tolerated at every binding site: the highest affinity site in the mouse metallothionein I gene, MREd, is unaffected by methylation, while two other MRE sites with CpGs at different positions are rendered partially or completely nonfunctional by methylation. Both methylation sensitive and insensitive factors/binding sites are likely to determine the developmental expression pattern of a gene.
AB - Cytosine methylation at CpG sites is often negatively correlated with mammalian gene activity. Many transcription factors whose DNA binding site contains one or more CpG dinucleotides are no longer able to efficiently bind DNA when the site is methylated. A notable exception is the zinc finger factor Sp1 which binds DNA and activates transcription even when its binding site is methylated. Here we show that two other zinc finger factors, MTF-1 and Krox-20, can also bind to CPG methylated sites. MTF-1 regulates metallothionein gene transcription by binding to a number of metal responsive elements (MREs), and Krox-20 regulates Hox genes during hindbrain segmentation. However, a refined analysis of MTF-1/MRE binding shows that methylation is not tolerated at every binding site: the highest affinity site in the mouse metallothionein I gene, MREd, is unaffected by methylation, while two other MRE sites with CpGs at different positions are rendered partially or completely nonfunctional by methylation. Both methylation sensitive and insensitive factors/binding sites are likely to determine the developmental expression pattern of a gene.
KW - DNA methylation
KW - Krox-20
KW - MTF-1
KW - Metal-responsive element (MRE)
KW - Zinc finger transcription factors
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U2 - 10.1515/bchm3.1996.377.1.47
DO - 10.1515/bchm3.1996.377.1.47
M3 - Article
C2 - 8929813
AN - SCOPUS:0030044251
SN - 0177-3593
VL - 377
SP - 47
EP - 56
JO - Biological chemistry Hoppe-Seyler
JF - Biological chemistry Hoppe-Seyler
IS - 1
ER -