ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Publication Date: 2008-03-07
    Description: Methylation of CpG dinucleotides is generally associated with epigenetic silencing of transcription and is maintained through cellular division. Multiple CpG sequences are rare in mammalian genomes, but frequently occur at the transcriptional start site of active genes, with most clusters of CpGs being hypomethylated. We reported previously that the proximal region of the trefoil factor 1 (TFF1, also known as pS2) and oestrogen receptor alpha (ERalpha) promoters could be partially methylated by treatment with deacetylase inhibitors, suggesting the possibility of dynamic changes in DNA methylation. Here we show that cyclical methylation and demethylation of CpG dinucleotides, with a periodicity of around 100 min, is characteristic for five selected promoters, including the oestrogen (E2)-responsive pS2 gene, in human cells. When the pS2 gene is actively transcribed, DNA methylation occurs after the cyclical occupancy of ERalpha and RNA polymerase II (polII). Moreover, we report conditions that provoke methylation cycling of the pS2 promoter in cell lines in which pS2 expression is quiescent and the proximal promoter is methylated. This coincides with a low-level re-expression of ERalpha and of pS2 transcripts.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kangaspeska, Sara -- Stride, Brenda -- Metivier, Raphael -- Polycarpou-Schwarz, Maria -- Ibberson, David -- Carmouche, Richard Paul -- Benes, Vladimir -- Gannon, Frank -- Reid, George -- England -- Nature. 2008 Mar 6;452(7183):112-5. doi: 10.1038/nature06640.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉European Molecular Biology Laboratory, Meyerhofstrasse 1, D-69117 Heidelberg, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18322535" target="_blank"〉PubMed〈/a〉
    Keywords: Cell Line, Tumor ; CpG Islands/genetics ; DNA/genetics/*metabolism ; *DNA Methylation/drug effects ; Doxorubicin/pharmacology ; Estrogen Receptor alpha/genetics/metabolism ; *Gene Expression Regulation/drug effects ; Humans ; Promoter Regions, Genetic/*genetics ; RNA Polymerase II/metabolism ; RNA, Messenger/genetics/metabolism ; Time Factors ; Transcription, Genetic/drug effects ; Tumor Suppressor Proteins/genetics
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Publication Date: 2008-03-07
    Description: Processes that regulate gene transcription are directly under the influence of the genome organization. The epigenome contains additional information that is not brought by DNA sequence, and generates spatial and functional constraints that complement genetic instructions. DNA methylation on CpGs constitutes an epigenetic mark generally correlated with transcriptionally silent condensed chromatin. Replication of methylation patterns by DNA methyltransferases maintains genome stability through cell division. Here we present evidence of an unanticipated dynamic role for DNA methylation in gene regulation in human cells. Periodic, strand-specific methylation/demethylation occurs during transcriptional cycling of the pS2/TFF1 gene promoter on activation by oestrogens. DNA methyltransferases exhibit dual actions during these cycles, being involved in CpG methylation and active demethylation of 5mCpGs through deamination. Inhibition of this process precludes demethylation of the pS2 gene promoter and its subsequent transcriptional activation. Cyclical changes in the methylation status of promoter CpGs may thus represent a critical event in transcriptional achievement.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Metivier, Raphael -- Gallais, Rozenn -- Tiffoche, Christophe -- Le Peron, Christine -- Jurkowska, Renata Z -- Carmouche, Richard P -- Ibberson, David -- Barath, Peter -- Demay, Florence -- Reid, George -- Benes, Vladimir -- Jeltsch, Albert -- Gannon, Frank -- Salbert, Gilles -- England -- Nature. 2008 Mar 6;452(7183):45-50. doi: 10.1038/nature06544.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Universite de Rennes I, CNRS, UMR 6026 Equipe SPARTE, IFR 140 GFAS, Campus de Beaulieu, 35042 Rennes cedex, France. Raphael.Metivier@univ-rennes1.fr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18322525" target="_blank"〉PubMed〈/a〉
    Keywords: Cell Line ; Chromatin Immunoprecipitation ; CpG Islands/genetics ; DNA (Cytosine-5-)-Methyltransferase/antagonists & inhibitors/metabolism ; *DNA Methylation/drug effects ; DNA Repair ; Deamination ; Estrogens/pharmacology ; *Gene Expression Regulation/drug effects ; Humans ; Kinetics ; Promoter Regions, Genetic/*genetics ; Thymine DNA Glycosylase/metabolism ; Transcription, Genetic/drug effects/*genetics ; Transcriptional Activation/drug effects/*genetics ; Tumor Suppressor Proteins/*genetics
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    facet.materialart.
    Unknown
    Kingston, Jamaica : Periodicals Archive Online (PAO)
    Social and economic studies. 5:1 (1956:Mar.) 93 
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Publication Date: 2018-07-30
    Print ISSN: 0003-6951
    Electronic ISSN: 1077-3118
    Topics: Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...