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Chromosomal copy number variation reveals differential levels of genomic plasticity in distinct Trypanosoma cruzi strains
BACKGROUND: Trypanosoma cruzi, the etiologic agent of Chagas disease, is currently divided into six discrete typing units (DTUs), named TcI–TcVI. CL Brener, the reference strain of the T. cruzi genome project, is a hybrid with a genome assembled into 41 putative chromosomes. Gene copy number variati...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491234/ https://www.ncbi.nlm.nih.gov/pubmed/26141959 http://dx.doi.org/10.1186/s12864-015-1680-4 |
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author | Reis-Cunha, João Luís Rodrigues-Luiz, Gabriela F. Valdivia, Hugo O. Baptista, Rodrigo P. Mendes, Tiago A. O. de Morais, Guilherme Loss Guedes, Rafael Macedo, Andrea M. Bern, Caryn Gilman, Robert H. Lopez, Carlos Talavera Andersson, Björn Vasconcelos, Ana Tereza Bartholomeu, Daniella C. |
author_facet | Reis-Cunha, João Luís Rodrigues-Luiz, Gabriela F. Valdivia, Hugo O. Baptista, Rodrigo P. Mendes, Tiago A. O. de Morais, Guilherme Loss Guedes, Rafael Macedo, Andrea M. Bern, Caryn Gilman, Robert H. Lopez, Carlos Talavera Andersson, Björn Vasconcelos, Ana Tereza Bartholomeu, Daniella C. |
author_sort | Reis-Cunha, João Luís |
collection | PubMed |
description | BACKGROUND: Trypanosoma cruzi, the etiologic agent of Chagas disease, is currently divided into six discrete typing units (DTUs), named TcI–TcVI. CL Brener, the reference strain of the T. cruzi genome project, is a hybrid with a genome assembled into 41 putative chromosomes. Gene copy number variation (CNV) is well documented as an important mechanism to enhance gene expression and variability in T. cruzi. Chromosomal CNV (CCNV) is another level of gene CNV in which whole blocks of genes are expanded simultaneously. Although the T. cruzi karyotype is not well defined, several studies have demonstrated a significant variation in the size and content of chromosomes between different T. cruzi strains. Despite these studies, the extent of diversity in CCNV among T. cruzi strains based on a read depth coverage analysis has not been determined. RESULTS: We identify the CCNV in T. cruzi strains from the TcI, TcII and TcIII DTUs, by analyzing the depth coverage of short reads from these strains using the 41 CL Brener chromosomes as reference. This study led to the identification of a broader extent of CCNV in T. cruzi than was previously speculated. The TcI DTU strains have very few aneuploidies, while the strains from TcII and TcIII DTUs present a high degree of chromosomal expansions. Chromosome 31, which is the only chromosome that is supernumerary in all six T. cruzi samples evaluated in this study, is enriched with genes related to glycosylation pathways, highlighting the importance of glycosylation to parasite survival. CONCLUSIONS: Increased gene copy number due to chromosome amplification may contribute to alterations in gene expression, which represents a strategy that may be crucial for parasites that mainly depend on post-transcriptional mechanisms to control gene expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1680-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4491234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44912342015-07-05 Chromosomal copy number variation reveals differential levels of genomic plasticity in distinct Trypanosoma cruzi strains Reis-Cunha, João Luís Rodrigues-Luiz, Gabriela F. Valdivia, Hugo O. Baptista, Rodrigo P. Mendes, Tiago A. O. de Morais, Guilherme Loss Guedes, Rafael Macedo, Andrea M. Bern, Caryn Gilman, Robert H. Lopez, Carlos Talavera Andersson, Björn Vasconcelos, Ana Tereza Bartholomeu, Daniella C. BMC Genomics Research Article BACKGROUND: Trypanosoma cruzi, the etiologic agent of Chagas disease, is currently divided into six discrete typing units (DTUs), named TcI–TcVI. CL Brener, the reference strain of the T. cruzi genome project, is a hybrid with a genome assembled into 41 putative chromosomes. Gene copy number variation (CNV) is well documented as an important mechanism to enhance gene expression and variability in T. cruzi. Chromosomal CNV (CCNV) is another level of gene CNV in which whole blocks of genes are expanded simultaneously. Although the T. cruzi karyotype is not well defined, several studies have demonstrated a significant variation in the size and content of chromosomes between different T. cruzi strains. Despite these studies, the extent of diversity in CCNV among T. cruzi strains based on a read depth coverage analysis has not been determined. RESULTS: We identify the CCNV in T. cruzi strains from the TcI, TcII and TcIII DTUs, by analyzing the depth coverage of short reads from these strains using the 41 CL Brener chromosomes as reference. This study led to the identification of a broader extent of CCNV in T. cruzi than was previously speculated. The TcI DTU strains have very few aneuploidies, while the strains from TcII and TcIII DTUs present a high degree of chromosomal expansions. Chromosome 31, which is the only chromosome that is supernumerary in all six T. cruzi samples evaluated in this study, is enriched with genes related to glycosylation pathways, highlighting the importance of glycosylation to parasite survival. CONCLUSIONS: Increased gene copy number due to chromosome amplification may contribute to alterations in gene expression, which represents a strategy that may be crucial for parasites that mainly depend on post-transcriptional mechanisms to control gene expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1680-4) contains supplementary material, which is available to authorized users. BioMed Central 2015-07-04 /pmc/articles/PMC4491234/ /pubmed/26141959 http://dx.doi.org/10.1186/s12864-015-1680-4 Text en © Reis-Cunha et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Reis-Cunha, João Luís Rodrigues-Luiz, Gabriela F. Valdivia, Hugo O. Baptista, Rodrigo P. Mendes, Tiago A. O. de Morais, Guilherme Loss Guedes, Rafael Macedo, Andrea M. Bern, Caryn Gilman, Robert H. Lopez, Carlos Talavera Andersson, Björn Vasconcelos, Ana Tereza Bartholomeu, Daniella C. Chromosomal copy number variation reveals differential levels of genomic plasticity in distinct Trypanosoma cruzi strains |
title | Chromosomal copy number variation reveals differential levels of genomic plasticity in distinct Trypanosoma cruzi strains |
title_full | Chromosomal copy number variation reveals differential levels of genomic plasticity in distinct Trypanosoma cruzi strains |
title_fullStr | Chromosomal copy number variation reveals differential levels of genomic plasticity in distinct Trypanosoma cruzi strains |
title_full_unstemmed | Chromosomal copy number variation reveals differential levels of genomic plasticity in distinct Trypanosoma cruzi strains |
title_short | Chromosomal copy number variation reveals differential levels of genomic plasticity in distinct Trypanosoma cruzi strains |
title_sort | chromosomal copy number variation reveals differential levels of genomic plasticity in distinct trypanosoma cruzi strains |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491234/ https://www.ncbi.nlm.nih.gov/pubmed/26141959 http://dx.doi.org/10.1186/s12864-015-1680-4 |
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