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...

Full description

Bibliographic Details
Main Authors: Tretina, Kyle, Pelle, Roger, Silva, Joana C.
Format: Journal Article
Language:Inglés
Published: Springer 2016
Subjects:
Online Access:https://hdl.handle.net/10568/82993
_version_ 1855515329781825536
author Tretina, Kyle
Pelle, Roger
Silva, Joana C.
author_browse Pelle, Roger
Silva, Joana C.
Tretina, Kyle
author_facet Tretina, Kyle
Pelle, Roger
Silva, Joana C.
author_sort Tretina, Kyle
collection Repository of Agricultural Research Outputs (CGSpace)
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.
format Journal Article
id CGSpace82993
institution CGIAR Consortium
language Inglés
publishDate 2016
publishDateRange 2016
publishDateSort 2016
publisher Springer
publisherStr Springer
record_format dspace
spelling CGSpace829932023-12-08T19:36:04Z Cis regulatory motifs and antisense transcriptional control in the apicomplexan Theileria parva Tretina, Kyle Pelle, Roger Silva, Joana C. animal diseases cattle parasites phenotypes theileria parva genetics biotechnology 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. 2016-12 2017-08-02T09:41:14Z 2017-08-02T09:41:14Z Journal Article https://hdl.handle.net/10568/82993 en Open Access Springer Tretina, K., Pelle, R. and Silva, J.C. 2016. Cis regulatory motifs and antisense transcriptional control in the apicomplexan Theileria parva. BMC Genomics 17(1):1.
spellingShingle animal diseases
cattle
parasites
phenotypes
theileria parva
genetics
biotechnology
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 animal diseases
cattle
parasites
phenotypes
theileria parva
genetics
biotechnology
url https://hdl.handle.net/10568/82993
work_keys_str_mv AT tretinakyle cisregulatorymotifsandantisensetranscriptionalcontrolintheapicomplexantheileriaparva
AT pelleroger cisregulatorymotifsandantisensetranscriptionalcontrolintheapicomplexantheileriaparva
AT silvajoanac cisregulatorymotifsandantisensetranscriptionalcontrolintheapicomplexantheileriaparva