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Comparative Transcriptional and Genomic Analysis of Plasmodium falciparum Field Isolates

Mechanisms for differential regulation of gene expression may underlie much of the phenotypic variation and adaptability of malaria parasites. Here we describe transcriptional variation among culture-adapted field isolates of Plasmodium falciparum, the species responsible for most malarial disease....

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Autores principales: Mackinnon, Margaret J., Li, Jinguang, Mok, Sachel, Kortok, Moses M., Marsh, Kevin, Preiser, Peter R., Bozdech, Zbynek
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2764095/
https://www.ncbi.nlm.nih.gov/pubmed/19898609
http://dx.doi.org/10.1371/journal.ppat.1000644
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author Mackinnon, Margaret J.
Li, Jinguang
Mok, Sachel
Kortok, Moses M.
Marsh, Kevin
Preiser, Peter R.
Bozdech, Zbynek
author_facet Mackinnon, Margaret J.
Li, Jinguang
Mok, Sachel
Kortok, Moses M.
Marsh, Kevin
Preiser, Peter R.
Bozdech, Zbynek
author_sort Mackinnon, Margaret J.
collection PubMed
description Mechanisms for differential regulation of gene expression may underlie much of the phenotypic variation and adaptability of malaria parasites. Here we describe transcriptional variation among culture-adapted field isolates of Plasmodium falciparum, the species responsible for most malarial disease. It was found that genes coding for parasite protein export into the red cell cytosol and onto its surface, and genes coding for sexual stage proteins involved in parasite transmission are up-regulated in field isolates compared with long-term laboratory isolates. Much of this variability was associated with the loss of small or large chromosomal segments, or other forms of gene copy number variation that are prevalent in the P. falciparum genome (copy number variants, CNVs). Expression levels of genes inside these segments were correlated to that of genes outside and adjacent to the segment boundaries, and this association declined with distance from the CNV boundary. This observation could not be explained by copy number variation in these adjacent genes. This suggests a local-acting regulatory role for CNVs in transcription of neighboring genes and helps explain the chromosomal clustering that we observed here. Transcriptional co-regulation of physical clusters of adaptive genes may provide a way for the parasite to readily adapt to its highly heterogeneous and strongly selective environment.
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spelling pubmed-27640952009-11-06 Comparative Transcriptional and Genomic Analysis of Plasmodium falciparum Field Isolates Mackinnon, Margaret J. Li, Jinguang Mok, Sachel Kortok, Moses M. Marsh, Kevin Preiser, Peter R. Bozdech, Zbynek PLoS Pathog Research Article Mechanisms for differential regulation of gene expression may underlie much of the phenotypic variation and adaptability of malaria parasites. Here we describe transcriptional variation among culture-adapted field isolates of Plasmodium falciparum, the species responsible for most malarial disease. It was found that genes coding for parasite protein export into the red cell cytosol and onto its surface, and genes coding for sexual stage proteins involved in parasite transmission are up-regulated in field isolates compared with long-term laboratory isolates. Much of this variability was associated with the loss of small or large chromosomal segments, or other forms of gene copy number variation that are prevalent in the P. falciparum genome (copy number variants, CNVs). Expression levels of genes inside these segments were correlated to that of genes outside and adjacent to the segment boundaries, and this association declined with distance from the CNV boundary. This observation could not be explained by copy number variation in these adjacent genes. This suggests a local-acting regulatory role for CNVs in transcription of neighboring genes and helps explain the chromosomal clustering that we observed here. Transcriptional co-regulation of physical clusters of adaptive genes may provide a way for the parasite to readily adapt to its highly heterogeneous and strongly selective environment. Public Library of Science 2009-10-30 /pmc/articles/PMC2764095/ /pubmed/19898609 http://dx.doi.org/10.1371/journal.ppat.1000644 Text en Mackinnon et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Mackinnon, Margaret J.
Li, Jinguang
Mok, Sachel
Kortok, Moses M.
Marsh, Kevin
Preiser, Peter R.
Bozdech, Zbynek
Comparative Transcriptional and Genomic Analysis of Plasmodium falciparum Field Isolates
title Comparative Transcriptional and Genomic Analysis of Plasmodium falciparum Field Isolates
title_full Comparative Transcriptional and Genomic Analysis of Plasmodium falciparum Field Isolates
title_fullStr Comparative Transcriptional and Genomic Analysis of Plasmodium falciparum Field Isolates
title_full_unstemmed Comparative Transcriptional and Genomic Analysis of Plasmodium falciparum Field Isolates
title_short Comparative Transcriptional and Genomic Analysis of Plasmodium falciparum Field Isolates
title_sort comparative transcriptional and genomic analysis of plasmodium falciparum field isolates
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2764095/
https://www.ncbi.nlm.nih.gov/pubmed/19898609
http://dx.doi.org/10.1371/journal.ppat.1000644
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