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A CpG island promoter drives the CXXC5 gene expression
CXXC5 is a member of the zinc-finger CXXC family that binds to unmethylated CpG dinucleotides. CXXC5 modulates gene expressions resulting in diverse cellular events mediated by distinct signaling pathways. However, the mechanism responsible for CXXC5 expression remains largely unknown. We found here...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329181/ https://www.ncbi.nlm.nih.gov/pubmed/34341443 http://dx.doi.org/10.1038/s41598-021-95165-6 |
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author | Yaşar, Pelin Kars, Gizem Yavuz, Kerim Ayaz, Gamze Oğuztüzün, Çerağ Bilgen, Ecenaz Suvacı, Zeynep Çetinkol, Özgül Persil Can, Tolga Muyan, Mesut |
author_facet | Yaşar, Pelin Kars, Gizem Yavuz, Kerim Ayaz, Gamze Oğuztüzün, Çerağ Bilgen, Ecenaz Suvacı, Zeynep Çetinkol, Özgül Persil Can, Tolga Muyan, Mesut |
author_sort | Yaşar, Pelin |
collection | PubMed |
description | CXXC5 is a member of the zinc-finger CXXC family that binds to unmethylated CpG dinucleotides. CXXC5 modulates gene expressions resulting in diverse cellular events mediated by distinct signaling pathways. However, the mechanism responsible for CXXC5 expression remains largely unknown. We found here that of the 14 annotated CXXC5 transcripts with distinct 5′ untranslated regions encoding the same protein, transcript variant 2 with the highest expression level among variants represents the main transcript in cell models. The DNA segment in and at the immediate 5′-sequences of the first exon of variant 2 contains a core promoter within which multiple transcription start sites are present. Residing in a region with high G–C nucleotide content and CpG repeats, the core promoter is unmethylated, deficient in nucleosomes, and associated with active RNA polymerase-II. These findings suggest that a CpG island promoter drives CXXC5 expression. Promoter pull-down revealed the association of various transcription factors (TFs) and transcription co-regulatory proteins, as well as proteins involved in histone/chromatin, DNA, and RNA processing with the core promoter. Of the TFs, we verified that ELF1 and MAZ contribute to CXXC5 expression. Moreover, the first exon of variant 2 may contain a G-quadruplex forming region that could modulate CXXC5 expression. |
format | Online Article Text |
id | pubmed-8329181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83291812021-08-04 A CpG island promoter drives the CXXC5 gene expression Yaşar, Pelin Kars, Gizem Yavuz, Kerim Ayaz, Gamze Oğuztüzün, Çerağ Bilgen, Ecenaz Suvacı, Zeynep Çetinkol, Özgül Persil Can, Tolga Muyan, Mesut Sci Rep Article CXXC5 is a member of the zinc-finger CXXC family that binds to unmethylated CpG dinucleotides. CXXC5 modulates gene expressions resulting in diverse cellular events mediated by distinct signaling pathways. However, the mechanism responsible for CXXC5 expression remains largely unknown. We found here that of the 14 annotated CXXC5 transcripts with distinct 5′ untranslated regions encoding the same protein, transcript variant 2 with the highest expression level among variants represents the main transcript in cell models. The DNA segment in and at the immediate 5′-sequences of the first exon of variant 2 contains a core promoter within which multiple transcription start sites are present. Residing in a region with high G–C nucleotide content and CpG repeats, the core promoter is unmethylated, deficient in nucleosomes, and associated with active RNA polymerase-II. These findings suggest that a CpG island promoter drives CXXC5 expression. Promoter pull-down revealed the association of various transcription factors (TFs) and transcription co-regulatory proteins, as well as proteins involved in histone/chromatin, DNA, and RNA processing with the core promoter. Of the TFs, we verified that ELF1 and MAZ contribute to CXXC5 expression. Moreover, the first exon of variant 2 may contain a G-quadruplex forming region that could modulate CXXC5 expression. Nature Publishing Group UK 2021-08-02 /pmc/articles/PMC8329181/ /pubmed/34341443 http://dx.doi.org/10.1038/s41598-021-95165-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yaşar, Pelin Kars, Gizem Yavuz, Kerim Ayaz, Gamze Oğuztüzün, Çerağ Bilgen, Ecenaz Suvacı, Zeynep Çetinkol, Özgül Persil Can, Tolga Muyan, Mesut A CpG island promoter drives the CXXC5 gene expression |
title | A CpG island promoter drives the CXXC5 gene expression |
title_full | A CpG island promoter drives the CXXC5 gene expression |
title_fullStr | A CpG island promoter drives the CXXC5 gene expression |
title_full_unstemmed | A CpG island promoter drives the CXXC5 gene expression |
title_short | A CpG island promoter drives the CXXC5 gene expression |
title_sort | cpg island promoter drives the cxxc5 gene expression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329181/ https://www.ncbi.nlm.nih.gov/pubmed/34341443 http://dx.doi.org/10.1038/s41598-021-95165-6 |
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