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A transcriptional factor B paralog functions as an activator to DNA damage-responsive expression in archaea
Previously it was shown that UV irradiation induces a strong upregulation of tfb3 coding for a paralog of the archaeal transcriptional factor B (TFB) in Sulfolobus solfataricus, a crenarchaea. To investigate the function of this gene in DNA damage response (DDR), tfb3 was inactivated by gene deletio...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6101594/ https://www.ncbi.nlm.nih.gov/pubmed/29618058 http://dx.doi.org/10.1093/nar/gky236 |
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author | Feng, Xu Sun, Mengmeng Han, Wenyuan Liang, Yun Xiang She, Qunxin |
author_facet | Feng, Xu Sun, Mengmeng Han, Wenyuan Liang, Yun Xiang She, Qunxin |
author_sort | Feng, Xu |
collection | PubMed |
description | Previously it was shown that UV irradiation induces a strong upregulation of tfb3 coding for a paralog of the archaeal transcriptional factor B (TFB) in Sulfolobus solfataricus, a crenarchaea. To investigate the function of this gene in DNA damage response (DDR), tfb3 was inactivated by gene deletion in Sulfolobus islandicus and the resulting Δtfb3 was more sensitive to DNA damage agents than the original strain. Transcriptome analysis revealed that a large set of genes show TFB3-dependent activation, including genes of the ups operon and ced system. Furthermore, the TFB3 protein was found to be associated with DDR gene promoters and functional dissection of TFB3 showed that the conserved Zn-ribbon and coiled-coil motif are essential for the activation. Together, the results indicated that TFB3 activates the expression of DDR genes by interaction with other transcriptional factors at the promoter regions of DDR genes to facilitate the formation of transcription initiation complex. Strikingly, TFB3 and Ced systems are present in a wide range of crenarchaea, suggesting that the Ced system function as a primary DNA damage repair mechanism in Crenarchaeota. Our findings further suggest that TFB3 and the concurrent TFB1 form a TFB3-dependent DNA damage-responsive circuit with their target genes, which is evolutionarily conserved in the major lineage of Archaea. |
format | Online Article Text |
id | pubmed-6101594 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61015942018-08-27 A transcriptional factor B paralog functions as an activator to DNA damage-responsive expression in archaea Feng, Xu Sun, Mengmeng Han, Wenyuan Liang, Yun Xiang She, Qunxin Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Previously it was shown that UV irradiation induces a strong upregulation of tfb3 coding for a paralog of the archaeal transcriptional factor B (TFB) in Sulfolobus solfataricus, a crenarchaea. To investigate the function of this gene in DNA damage response (DDR), tfb3 was inactivated by gene deletion in Sulfolobus islandicus and the resulting Δtfb3 was more sensitive to DNA damage agents than the original strain. Transcriptome analysis revealed that a large set of genes show TFB3-dependent activation, including genes of the ups operon and ced system. Furthermore, the TFB3 protein was found to be associated with DDR gene promoters and functional dissection of TFB3 showed that the conserved Zn-ribbon and coiled-coil motif are essential for the activation. Together, the results indicated that TFB3 activates the expression of DDR genes by interaction with other transcriptional factors at the promoter regions of DDR genes to facilitate the formation of transcription initiation complex. Strikingly, TFB3 and Ced systems are present in a wide range of crenarchaea, suggesting that the Ced system function as a primary DNA damage repair mechanism in Crenarchaeota. Our findings further suggest that TFB3 and the concurrent TFB1 form a TFB3-dependent DNA damage-responsive circuit with their target genes, which is evolutionarily conserved in the major lineage of Archaea. Oxford University Press 2018-08-21 2018-03-30 /pmc/articles/PMC6101594/ /pubmed/29618058 http://dx.doi.org/10.1093/nar/gky236 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene regulation, Chromatin and Epigenetics Feng, Xu Sun, Mengmeng Han, Wenyuan Liang, Yun Xiang She, Qunxin A transcriptional factor B paralog functions as an activator to DNA damage-responsive expression in archaea |
title | A transcriptional factor B paralog functions as an activator to DNA damage-responsive expression in archaea |
title_full | A transcriptional factor B paralog functions as an activator to DNA damage-responsive expression in archaea |
title_fullStr | A transcriptional factor B paralog functions as an activator to DNA damage-responsive expression in archaea |
title_full_unstemmed | A transcriptional factor B paralog functions as an activator to DNA damage-responsive expression in archaea |
title_short | A transcriptional factor B paralog functions as an activator to DNA damage-responsive expression in archaea |
title_sort | transcriptional factor b paralog functions as an activator to dna damage-responsive expression in archaea |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6101594/ https://www.ncbi.nlm.nih.gov/pubmed/29618058 http://dx.doi.org/10.1093/nar/gky236 |
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