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Genome-wide Analysis Reveals Extensive Functional Interaction between DNA Replication Initiation and Transcription in the Genome of Trypanosoma brucei
Identification of replication initiation sites, termed origins, is a crucial step in understanding genome transmission in any organism. Transcription of the Trypanosoma brucei genome is highly unusual, with each chromosome comprising a few discrete transcription units. To understand how DNA replicat...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607257/ https://www.ncbi.nlm.nih.gov/pubmed/22840408 http://dx.doi.org/10.1016/j.celrep.2012.06.007 |
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author | Tiengwe, Calvin Marcello, Lucio Farr, Helen Dickens, Nicholas Kelly, Steven Swiderski, Michal Vaughan, Diane Gull, Keith Barry, J. David Bell, Stephen D. McCulloch, Richard |
author_facet | Tiengwe, Calvin Marcello, Lucio Farr, Helen Dickens, Nicholas Kelly, Steven Swiderski, Michal Vaughan, Diane Gull, Keith Barry, J. David Bell, Stephen D. McCulloch, Richard |
author_sort | Tiengwe, Calvin |
collection | PubMed |
description | Identification of replication initiation sites, termed origins, is a crucial step in understanding genome transmission in any organism. Transcription of the Trypanosoma brucei genome is highly unusual, with each chromosome comprising a few discrete transcription units. To understand how DNA replication occurs in the context of such organization, we have performed genome-wide mapping of the binding sites of the replication initiator ORC1/CDC6 and have identified replication origins, revealing that both localize to the boundaries of the transcription units. A remarkably small number of active origins is seen, whose spacing is greater than in any other eukaryote. We show that replication and transcription in T. brucei have a profound functional overlap, as reducing ORC1/CDC6 levels leads to genome-wide increases in mRNA levels arising from the boundaries of the transcription units. In addition, ORC1/CDC6 loss causes derepression of silent Variant Surface Glycoprotein genes, which are critical for host immune evasion. |
format | Online Article Text |
id | pubmed-3607257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36072572013-03-25 Genome-wide Analysis Reveals Extensive Functional Interaction between DNA Replication Initiation and Transcription in the Genome of Trypanosoma brucei Tiengwe, Calvin Marcello, Lucio Farr, Helen Dickens, Nicholas Kelly, Steven Swiderski, Michal Vaughan, Diane Gull, Keith Barry, J. David Bell, Stephen D. McCulloch, Richard Cell Rep Resource Identification of replication initiation sites, termed origins, is a crucial step in understanding genome transmission in any organism. Transcription of the Trypanosoma brucei genome is highly unusual, with each chromosome comprising a few discrete transcription units. To understand how DNA replication occurs in the context of such organization, we have performed genome-wide mapping of the binding sites of the replication initiator ORC1/CDC6 and have identified replication origins, revealing that both localize to the boundaries of the transcription units. A remarkably small number of active origins is seen, whose spacing is greater than in any other eukaryote. We show that replication and transcription in T. brucei have a profound functional overlap, as reducing ORC1/CDC6 levels leads to genome-wide increases in mRNA levels arising from the boundaries of the transcription units. In addition, ORC1/CDC6 loss causes derepression of silent Variant Surface Glycoprotein genes, which are critical for host immune evasion. Cell Press 2012-07-26 /pmc/articles/PMC3607257/ /pubmed/22840408 http://dx.doi.org/10.1016/j.celrep.2012.06.007 Text en © 2012 The Authors https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Resource Tiengwe, Calvin Marcello, Lucio Farr, Helen Dickens, Nicholas Kelly, Steven Swiderski, Michal Vaughan, Diane Gull, Keith Barry, J. David Bell, Stephen D. McCulloch, Richard Genome-wide Analysis Reveals Extensive Functional Interaction between DNA Replication Initiation and Transcription in the Genome of Trypanosoma brucei |
title | Genome-wide Analysis Reveals Extensive Functional Interaction between DNA Replication Initiation and Transcription in the Genome of Trypanosoma brucei |
title_full | Genome-wide Analysis Reveals Extensive Functional Interaction between DNA Replication Initiation and Transcription in the Genome of Trypanosoma brucei |
title_fullStr | Genome-wide Analysis Reveals Extensive Functional Interaction between DNA Replication Initiation and Transcription in the Genome of Trypanosoma brucei |
title_full_unstemmed | Genome-wide Analysis Reveals Extensive Functional Interaction between DNA Replication Initiation and Transcription in the Genome of Trypanosoma brucei |
title_short | Genome-wide Analysis Reveals Extensive Functional Interaction between DNA Replication Initiation and Transcription in the Genome of Trypanosoma brucei |
title_sort | genome-wide analysis reveals extensive functional interaction between dna replication initiation and transcription in the genome of trypanosoma brucei |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607257/ https://www.ncbi.nlm.nih.gov/pubmed/22840408 http://dx.doi.org/10.1016/j.celrep.2012.06.007 |
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