RBPJ binds to consensus and methylated cis elements within phased nucleosomes and controls gene expression in human aortic smooth muscle cells in cooperation with SRF

التفاصيل البيبلوغرافية
العنوان: RBPJ binds to consensus and methylated cis elements within phased nucleosomes and controls gene expression in human aortic smooth muscle cells in cooperation with SRF
المؤلفون: Joan M. Taylor, Julian M. Rozenberg, Christopher P. Mack
المصدر: Nucleic acids research. 46(16)
سنة النشر: 2018
مصطلحات موضوعية: 0301 basic medicine, Serum Response Factor, Myocytes, Smooth Muscle, Repressor, Biology, Cell Line, 03 medical and health sciences, 0302 clinical medicine, Serum response factor, Gene expression, Genetics, Nucleosome, Humans, Aorta, Regulation of gene expression, Binding Sites, Base Sequence, RBPJ, Cell Differentiation, DNA Methylation, Chromatin, Cell biology, Nucleosomes, 030104 developmental biology, Enhancer Elements, Genetic, Gene Expression Regulation, Immunoglobulin J Recombination Signal Sequence-Binding Protein, Hypersensitive site, 030217 neurology & neurosurgery, Protein Binding
الوصف: Given our previous demonstration that RBPJ binds a methylated repressor element and regulates smooth muscle cell (SMC)-specific gene expression, we used genome-wide approaches to identify RBPJ binding regions in human aortic SMC and to assess RBPJ's effects on chromatin structure and gene expression. RBPJ bound to consensus cis elements, but also to TCmGGGA sequences within Alu repeats that were less transcriptionally active as assessed by DNAse hypersensitivity, H3K9 acetylation, and Notch3 and RNA Pol II binding. Interestingly, RBPJ binding was frequently detected at the borders of open chromatin, and a large fraction of genes induced or repressed by RBPJ depletion were associated with this cluster of RBPJ binding sites. RBPJ binding dramatically co-localized with serum response factor (SRF) and RNA seq experiments in RBPJ- and SRF-depleted SMC demonstrated that these factors interact functionally to regulate the contraction and inflammatory gene programs that help define SMC phenotype. Finally, we showed that RBPJ bound preferentially to phased nucleosomes independent of active chromatin marks and to cis elements positioned at the beginning and middle of the nucleosome dyad. These novel findings add important insight into RBPJ's role in chromatin structure and gene expression in SMC.
تدمد: 1362-4962
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd61f693d133cbf9851d92e96fa0e6ba
https://pubmed.ncbi.nlm.nih.gov/29931229
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....fd61f693d133cbf9851d92e96fa0e6ba
قاعدة البيانات: OpenAIRE