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Cis regulatory motifs and antisense transcriptional control in the apicomplexan Theileria parva
BACKGROUND: Theileria parva is an intracellular parasite that causes a lymphoproliferative disease in cattle. It does so by inducing cancer-like phenotypes in the host cells it infects, although the molecular and regulatory mechanisms involved remain poorly understood. RNAseq data, and the resulting...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4761415/ https://www.ncbi.nlm.nih.gov/pubmed/26896950 http://dx.doi.org/10.1186/s12864-016-2444-5 |
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author | Tretina, Kyle Pelle, Roger Silva, Joana C. |
author_facet | Tretina, Kyle Pelle, Roger Silva, Joana C. |
author_sort | Tretina, Kyle |
collection | PubMed |
description | BACKGROUND: Theileria parva is an intracellular parasite that causes a lymphoproliferative disease in cattle. It does so by inducing cancer-like phenotypes in the host cells it infects, although the molecular and regulatory mechanisms involved remain poorly understood. RNAseq data, and the resulting updated genome annotation now available for this parasite, offer an unprecedented opportunity to characterize the genomic features associated with gene regulation in this species. Our previous analyses revealed a T. parva genome even more gene-dense than previously thought, with many adjacent loci overlapping each other, not only at the level of untranslated sequences (UTRs) but even in coding sequences. RESULTS: Despite this compactness, Theileria intergenic regions show a pattern of size distribution indicative of monocistronic gene transcription. Three previously described motifs are conserved among Theileria species and highly prevalent in promoter regions near or at the transcription start sites. We found novel motifs at many transcription termination sites, as well as upstream of parasite genes thought to be critical for host transformation. Adjacent genes that could be regulated by antisense transcription from an overlapping transcriptional unit are syntenic between T. parva and P. falciparum at a frequency higher than expected by chance, suggesting the presence of common, and evolutionary old, regulatory mechanisms in the phylum Apicomplexa. CONCLUSIONS: We propose a model of transcription with conserved sense and antisense transcription from a few taxonomically ubiquitous and several species-specific promoter motifs. Interestingly, the gene networks regulated by conserved promoters are themselves, in most cases, not conserved between species or genera. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2444-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4761415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47614152016-02-22 Cis regulatory motifs and antisense transcriptional control in the apicomplexan Theileria parva Tretina, Kyle Pelle, Roger Silva, Joana C. BMC Genomics Research Article BACKGROUND: Theileria parva is an intracellular parasite that causes a lymphoproliferative disease in cattle. It does so by inducing cancer-like phenotypes in the host cells it infects, although the molecular and regulatory mechanisms involved remain poorly understood. RNAseq data, and the resulting updated genome annotation now available for this parasite, offer an unprecedented opportunity to characterize the genomic features associated with gene regulation in this species. Our previous analyses revealed a T. parva genome even more gene-dense than previously thought, with many adjacent loci overlapping each other, not only at the level of untranslated sequences (UTRs) but even in coding sequences. RESULTS: Despite this compactness, Theileria intergenic regions show a pattern of size distribution indicative of monocistronic gene transcription. Three previously described motifs are conserved among Theileria species and highly prevalent in promoter regions near or at the transcription start sites. We found novel motifs at many transcription termination sites, as well as upstream of parasite genes thought to be critical for host transformation. Adjacent genes that could be regulated by antisense transcription from an overlapping transcriptional unit are syntenic between T. parva and P. falciparum at a frequency higher than expected by chance, suggesting the presence of common, and evolutionary old, regulatory mechanisms in the phylum Apicomplexa. CONCLUSIONS: We propose a model of transcription with conserved sense and antisense transcription from a few taxonomically ubiquitous and several species-specific promoter motifs. Interestingly, the gene networks regulated by conserved promoters are themselves, in most cases, not conserved between species or genera. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2444-5) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-20 /pmc/articles/PMC4761415/ /pubmed/26896950 http://dx.doi.org/10.1186/s12864-016-2444-5 Text en © Tretina et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Tretina, Kyle Pelle, Roger Silva, Joana C. Cis regulatory motifs and antisense transcriptional control in the apicomplexan Theileria parva |
title | Cis regulatory motifs and antisense transcriptional control in the apicomplexan Theileria parva |
title_full | Cis regulatory motifs and antisense transcriptional control in the apicomplexan Theileria parva |
title_fullStr | Cis regulatory motifs and antisense transcriptional control in the apicomplexan Theileria parva |
title_full_unstemmed | Cis regulatory motifs and antisense transcriptional control in the apicomplexan Theileria parva |
title_short | Cis regulatory motifs and antisense transcriptional control in the apicomplexan Theileria parva |
title_sort | cis regulatory motifs and antisense transcriptional control in the apicomplexan theileria parva |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4761415/ https://www.ncbi.nlm.nih.gov/pubmed/26896950 http://dx.doi.org/10.1186/s12864-016-2444-5 |
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