Sequences conserved by selection across mouse and human malaria species

<p>Abstract</p> <p>Background</p> <p>Little is known, either experimentally or computationally, about the genomic sequence features that regulate malaria genes. A sequence conservation analysis of the malaria species <it>P. falciparum</it>, <it>P. berg...

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Main Authors: Chuang Jeffrey H, Persampieri Jason H, Imamura Hideo
Format: Article
Language:English
Published: BMC 2007-10-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/8/372
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spelling doaj-dc15374f87654adc87dd25c7305f27b12020-11-25T00:55:04ZengBMCBMC Genomics1471-21642007-10-018137210.1186/1471-2164-8-372Sequences conserved by selection across mouse and human malaria speciesChuang Jeffrey HPersampieri Jason HImamura Hideo<p>Abstract</p> <p>Background</p> <p>Little is known, either experimentally or computationally, about the genomic sequence features that regulate malaria genes. A sequence conservation analysis of the malaria species <it>P. falciparum</it>, <it>P. berghei</it>, <it>P. yoelii</it>, and <it>P. chabaudi </it>could significantly advance knowledge of malaria gene regulation.</p> <p>Results</p> <p>We computationally identify intergenic sequences conserved beyond neutral expectations, using a conservation algorithm that accounts for the strong compositional biases in malaria genomes. We first quantify the composition-specific divergence at silent positions in coding sequence. Using this as a background, we examine gene 5' regions, identifying 610 blocks conserved far beyond neutral expectations across the three mouse malariae, and 81 blocks conserved as strongly across all four species (p < 10<sup>-6</sup>). Detailed analysis of these blocks indicates that only a minor fraction are likely to be previously unknown coding sequences. Analogous noncoding conserved blocks have been shown to regulate adjacent genes in other phylogenies, making the predicted blocks excellent candidates for novel regulatory functions. We also find three potential transcription factor binding motifs which exhibit strong conservation and overrepresentation among the rodent malariae.</p> <p>Conclusion</p> <p>A broader finding of our analysis is that less malaria intergenic sequence has been conserved by selection than in yeast or vertebrate genomes. This supports the hypothesis that transcriptional regulation is simpler in malaria than other eukaryotic species. We have built a public database containing all sequence alignments and functional predictions, and we expect this to be a valuable resource to the malaria research community.</p> http://www.biomedcentral.com/1471-2164/8/372
collection DOAJ
language English
format Article
sources DOAJ
author Chuang Jeffrey H
Persampieri Jason H
Imamura Hideo
spellingShingle Chuang Jeffrey H
Persampieri Jason H
Imamura Hideo
Sequences conserved by selection across mouse and human malaria species
BMC Genomics
author_facet Chuang Jeffrey H
Persampieri Jason H
Imamura Hideo
author_sort Chuang Jeffrey H
title Sequences conserved by selection across mouse and human malaria species
title_short Sequences conserved by selection across mouse and human malaria species
title_full Sequences conserved by selection across mouse and human malaria species
title_fullStr Sequences conserved by selection across mouse and human malaria species
title_full_unstemmed Sequences conserved by selection across mouse and human malaria species
title_sort sequences conserved by selection across mouse and human malaria species
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2007-10-01
description <p>Abstract</p> <p>Background</p> <p>Little is known, either experimentally or computationally, about the genomic sequence features that regulate malaria genes. A sequence conservation analysis of the malaria species <it>P. falciparum</it>, <it>P. berghei</it>, <it>P. yoelii</it>, and <it>P. chabaudi </it>could significantly advance knowledge of malaria gene regulation.</p> <p>Results</p> <p>We computationally identify intergenic sequences conserved beyond neutral expectations, using a conservation algorithm that accounts for the strong compositional biases in malaria genomes. We first quantify the composition-specific divergence at silent positions in coding sequence. Using this as a background, we examine gene 5' regions, identifying 610 blocks conserved far beyond neutral expectations across the three mouse malariae, and 81 blocks conserved as strongly across all four species (p < 10<sup>-6</sup>). Detailed analysis of these blocks indicates that only a minor fraction are likely to be previously unknown coding sequences. Analogous noncoding conserved blocks have been shown to regulate adjacent genes in other phylogenies, making the predicted blocks excellent candidates for novel regulatory functions. We also find three potential transcription factor binding motifs which exhibit strong conservation and overrepresentation among the rodent malariae.</p> <p>Conclusion</p> <p>A broader finding of our analysis is that less malaria intergenic sequence has been conserved by selection than in yeast or vertebrate genomes. This supports the hypothesis that transcriptional regulation is simpler in malaria than other eukaryotic species. We have built a public database containing all sequence alignments and functional predictions, and we expect this to be a valuable resource to the malaria research community.</p>
url http://www.biomedcentral.com/1471-2164/8/372
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