Role of CTCF protein in regulating FMR1 locus transcription.
Fragile X syndrome (FXS), the leading cause of inherited intellectual disability, is caused by epigenetic silencing of the FMR1 gene, through expansion and methylation of a CGG triplet repeat (methylated full mutation). An antisense transcript (FMR1-AS1), starting from both promoter and intron 2 of...
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| Format: | Article |
| Language: | English |
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Public Library of Science (PLoS)
2013-01-01
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| Series: | PLoS Genetics |
| Online Access: | https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1003601&type=printable |
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| author | Stella Lanni Martina Goracci Loredana Borrelli Giorgia Mancano Pietro Chiurazzi Umberto Moscato Fabrizio Ferrè Manuela Helmer-Citterich Elisabetta Tabolacci Giovanni Neri |
| author_facet | Stella Lanni Martina Goracci Loredana Borrelli Giorgia Mancano Pietro Chiurazzi Umberto Moscato Fabrizio Ferrè Manuela Helmer-Citterich Elisabetta Tabolacci Giovanni Neri |
| author_sort | Stella Lanni |
| collection | DOAJ |
| description | Fragile X syndrome (FXS), the leading cause of inherited intellectual disability, is caused by epigenetic silencing of the FMR1 gene, through expansion and methylation of a CGG triplet repeat (methylated full mutation). An antisense transcript (FMR1-AS1), starting from both promoter and intron 2 of the FMR1 gene, was demonstrated in transcriptionally active alleles, but not in silent FXS alleles. Moreover, a DNA methylation boundary, which is lost in FXS, was recently identified upstream of the FMR1 gene. Several nuclear proteins bind to this region, like the insulator protein CTCF. Here we demonstrate for the first time that rare unmethylated full mutation (UFM) alleles present the same boundary described in wild type (WT) alleles and that CTCF binds to this region, as well as to the FMR1 gene promoter, exon 1 and intron 2 binding sites. Contrariwise, DNA methylation prevents CTCF binding to FXS alleles. Drug-induced CpGs demethylation does not restore this binding. CTCF knock-down experiments clearly established that CTCF does not act as insulator at the active FMR1 locus, despite the presence of a CGG expansion. CTCF depletion induces heterochromatinic histone configuration of the FMR1 locus and results in reduction of FMR1 transcription, which however is not accompanied by spreading of DNA methylation towards the FMR1 promoter. CTCF depletion is also associated with FMR1-AS1 mRNA reduction. Antisense RNA, like sense transcript, is upregulated in UFM and absent in FXS cells and its splicing is correlated to that of the FMR1-mRNA. We conclude that CTCF has a complex role in regulating FMR1 expression, probably through the organization of chromatin loops between sense/antisense transcriptional regulatory regions, as suggested by bioinformatics analysis. |
| format | Article |
| id | doaj-art-58b9bd3447b847228d228093a7ec2ba5 |
| institution | Kabale University |
| issn | 1553-7390 1553-7404 |
| language | English |
| publishDate | 2013-01-01 |
| publisher | Public Library of Science (PLoS) |
| record_format | Article |
| series | PLoS Genetics |
| spelling | doaj-art-58b9bd3447b847228d228093a7ec2ba52025-01-16T05:31:15ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042013-01-0197e100360110.1371/journal.pgen.1003601Role of CTCF protein in regulating FMR1 locus transcription.Stella LanniMartina GoracciLoredana BorrelliGiorgia MancanoPietro ChiurazziUmberto MoscatoFabrizio FerrèManuela Helmer-CitterichElisabetta TabolacciGiovanni NeriFragile X syndrome (FXS), the leading cause of inherited intellectual disability, is caused by epigenetic silencing of the FMR1 gene, through expansion and methylation of a CGG triplet repeat (methylated full mutation). An antisense transcript (FMR1-AS1), starting from both promoter and intron 2 of the FMR1 gene, was demonstrated in transcriptionally active alleles, but not in silent FXS alleles. Moreover, a DNA methylation boundary, which is lost in FXS, was recently identified upstream of the FMR1 gene. Several nuclear proteins bind to this region, like the insulator protein CTCF. Here we demonstrate for the first time that rare unmethylated full mutation (UFM) alleles present the same boundary described in wild type (WT) alleles and that CTCF binds to this region, as well as to the FMR1 gene promoter, exon 1 and intron 2 binding sites. Contrariwise, DNA methylation prevents CTCF binding to FXS alleles. Drug-induced CpGs demethylation does not restore this binding. CTCF knock-down experiments clearly established that CTCF does not act as insulator at the active FMR1 locus, despite the presence of a CGG expansion. CTCF depletion induces heterochromatinic histone configuration of the FMR1 locus and results in reduction of FMR1 transcription, which however is not accompanied by spreading of DNA methylation towards the FMR1 promoter. CTCF depletion is also associated with FMR1-AS1 mRNA reduction. Antisense RNA, like sense transcript, is upregulated in UFM and absent in FXS cells and its splicing is correlated to that of the FMR1-mRNA. We conclude that CTCF has a complex role in regulating FMR1 expression, probably through the organization of chromatin loops between sense/antisense transcriptional regulatory regions, as suggested by bioinformatics analysis.https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1003601&type=printable |
| spellingShingle | Stella Lanni Martina Goracci Loredana Borrelli Giorgia Mancano Pietro Chiurazzi Umberto Moscato Fabrizio Ferrè Manuela Helmer-Citterich Elisabetta Tabolacci Giovanni Neri Role of CTCF protein in regulating FMR1 locus transcription. PLoS Genetics |
| title | Role of CTCF protein in regulating FMR1 locus transcription. |
| title_full | Role of CTCF protein in regulating FMR1 locus transcription. |
| title_fullStr | Role of CTCF protein in regulating FMR1 locus transcription. |
| title_full_unstemmed | Role of CTCF protein in regulating FMR1 locus transcription. |
| title_short | Role of CTCF protein in regulating FMR1 locus transcription. |
| title_sort | role of ctcf protein in regulating fmr1 locus transcription |
| url | https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1003601&type=printable |
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