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Systematic identification of silencers in human cells

The majority of the human genome does not encode proteins. Many of these noncoding regions contain important regulatory sequences that control gene expression. To date, most studies have focused on activators such as enhancers, but regions that repress gene expression—silencers—have not been systema...

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Detalles Bibliográficos
Autores principales: Pang, Baoxu, Snyder, Michael P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148122/
https://www.ncbi.nlm.nih.gov/pubmed/32094911
http://dx.doi.org/10.1038/s41588-020-0578-5
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author Pang, Baoxu
Snyder, Michael P.
author_facet Pang, Baoxu
Snyder, Michael P.
author_sort Pang, Baoxu
collection PubMed
description The majority of the human genome does not encode proteins. Many of these noncoding regions contain important regulatory sequences that control gene expression. To date, most studies have focused on activators such as enhancers, but regions that repress gene expression—silencers—have not been systematically studied. We have developed a system that identifies silencer regions in a genome-wide fashion on the basis of silencer-mediated transcriptional repression of caspase 9. We found that silencers are widely distributed and may function in a tissue-specific fashion. These silencers harbor unique epigenetic signatures and are associated with specific transcription factors. Silencers also act at multiple genes, and at the level of chromosomal domains and long-range interactions. Deletion of silencer regions linked to the drug transporter genes ABCC2 and ABCG2 caused chemo-resistance. Overall, our study demonstrates that tissue-specific silencing is widespread throughout the human genome and likely contributes substantially to the regulation of gene expression and human biology.
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spelling pubmed-71481222020-08-24 Systematic identification of silencers in human cells Pang, Baoxu Snyder, Michael P. Nat Genet Article The majority of the human genome does not encode proteins. Many of these noncoding regions contain important regulatory sequences that control gene expression. To date, most studies have focused on activators such as enhancers, but regions that repress gene expression—silencers—have not been systematically studied. We have developed a system that identifies silencer regions in a genome-wide fashion on the basis of silencer-mediated transcriptional repression of caspase 9. We found that silencers are widely distributed and may function in a tissue-specific fashion. These silencers harbor unique epigenetic signatures and are associated with specific transcription factors. Silencers also act at multiple genes, and at the level of chromosomal domains and long-range interactions. Deletion of silencer regions linked to the drug transporter genes ABCC2 and ABCG2 caused chemo-resistance. Overall, our study demonstrates that tissue-specific silencing is widespread throughout the human genome and likely contributes substantially to the regulation of gene expression and human biology. 2020-02-24 2020-03 /pmc/articles/PMC7148122/ /pubmed/32094911 http://dx.doi.org/10.1038/s41588-020-0578-5 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Pang, Baoxu
Snyder, Michael P.
Systematic identification of silencers in human cells
title Systematic identification of silencers in human cells
title_full Systematic identification of silencers in human cells
title_fullStr Systematic identification of silencers in human cells
title_full_unstemmed Systematic identification of silencers in human cells
title_short Systematic identification of silencers in human cells
title_sort systematic identification of silencers in human cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148122/
https://www.ncbi.nlm.nih.gov/pubmed/32094911
http://dx.doi.org/10.1038/s41588-020-0578-5
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