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Transcription profiling during the cell cycle shows that a subset of Polycomb-targeted genes is upregulated during DNA replication
Genome-wide gene expression analyses of the human somatic cell cycle have indicated that the set of cycling genes differ between primary and cancer cells. By identifying genes that have cell cycle dependent expression in HaCaT human keratinocytes and comparing these with previously identified cell c...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3597645/ https://www.ncbi.nlm.nih.gov/pubmed/23325852 http://dx.doi.org/10.1093/nar/gks1336 |
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author | Peña-Diaz, Javier Hegre, Siv A. Anderssen, Endre Aas, Per A. Mjelle, Robin Gilfillan, Gregor D. Lyle, Robert Drabløs, Finn Krokan, Hans E. Sætrom, Pål |
author_facet | Peña-Diaz, Javier Hegre, Siv A. Anderssen, Endre Aas, Per A. Mjelle, Robin Gilfillan, Gregor D. Lyle, Robert Drabløs, Finn Krokan, Hans E. Sætrom, Pål |
author_sort | Peña-Diaz, Javier |
collection | PubMed |
description | Genome-wide gene expression analyses of the human somatic cell cycle have indicated that the set of cycling genes differ between primary and cancer cells. By identifying genes that have cell cycle dependent expression in HaCaT human keratinocytes and comparing these with previously identified cell cycle genes, we have identified three distinct groups of cell cycle genes. First, housekeeping genes enriched for known cell cycle functions; second, cell type-specific genes enriched for HaCaT-specific functions; and third, Polycomb-regulated genes. These Polycomb-regulated genes are specifically upregulated during DNA replication, and consistent with being epigenetically silenced in other cell cycle phases, these genes have lower expression than other cell cycle genes. We also find similar patterns in foreskin fibroblasts, indicating that replication-dependent expression of Polycomb-silenced genes is a prevalent but unrecognized regulatory mechanism. |
format | Online Article Text |
id | pubmed-3597645 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35976452013-03-15 Transcription profiling during the cell cycle shows that a subset of Polycomb-targeted genes is upregulated during DNA replication Peña-Diaz, Javier Hegre, Siv A. Anderssen, Endre Aas, Per A. Mjelle, Robin Gilfillan, Gregor D. Lyle, Robert Drabløs, Finn Krokan, Hans E. Sætrom, Pål Nucleic Acids Res Gene Regulation, Chromatin and Epigenetics Genome-wide gene expression analyses of the human somatic cell cycle have indicated that the set of cycling genes differ between primary and cancer cells. By identifying genes that have cell cycle dependent expression in HaCaT human keratinocytes and comparing these with previously identified cell cycle genes, we have identified three distinct groups of cell cycle genes. First, housekeeping genes enriched for known cell cycle functions; second, cell type-specific genes enriched for HaCaT-specific functions; and third, Polycomb-regulated genes. These Polycomb-regulated genes are specifically upregulated during DNA replication, and consistent with being epigenetically silenced in other cell cycle phases, these genes have lower expression than other cell cycle genes. We also find similar patterns in foreskin fibroblasts, indicating that replication-dependent expression of Polycomb-silenced genes is a prevalent but unrecognized regulatory mechanism. Oxford University Press 2013-03 2013-01-15 /pmc/articles/PMC3597645/ /pubmed/23325852 http://dx.doi.org/10.1093/nar/gks1336 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene Regulation, Chromatin and Epigenetics Peña-Diaz, Javier Hegre, Siv A. Anderssen, Endre Aas, Per A. Mjelle, Robin Gilfillan, Gregor D. Lyle, Robert Drabløs, Finn Krokan, Hans E. Sætrom, Pål Transcription profiling during the cell cycle shows that a subset of Polycomb-targeted genes is upregulated during DNA replication |
title | Transcription profiling during the cell cycle shows that a subset of Polycomb-targeted genes is upregulated during DNA replication |
title_full | Transcription profiling during the cell cycle shows that a subset of Polycomb-targeted genes is upregulated during DNA replication |
title_fullStr | Transcription profiling during the cell cycle shows that a subset of Polycomb-targeted genes is upregulated during DNA replication |
title_full_unstemmed | Transcription profiling during the cell cycle shows that a subset of Polycomb-targeted genes is upregulated during DNA replication |
title_short | Transcription profiling during the cell cycle shows that a subset of Polycomb-targeted genes is upregulated during DNA replication |
title_sort | transcription profiling during the cell cycle shows that a subset of polycomb-targeted genes is upregulated during dna replication |
topic | Gene Regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3597645/ https://www.ncbi.nlm.nih.gov/pubmed/23325852 http://dx.doi.org/10.1093/nar/gks1336 |
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