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Evolutionary dynamics of a conserved sequence motif in the ribosomal genes of the ciliate Paramecium

BACKGROUND: In protozoa, the identification of preserved motifs by comparative genomics is often impeded by difficulties to generate reliable alignments for non-coding sequences. Moreover, the evolutionary dynamics of regulatory elements in 3' untranslated regions (both in protozoa and metazoa)...

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Autores principales: Catania, Francesco, Lynch, Michael
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874801/
https://www.ncbi.nlm.nih.gov/pubmed/20441586
http://dx.doi.org/10.1186/1471-2148-10-129
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author Catania, Francesco
Lynch, Michael
author_facet Catania, Francesco
Lynch, Michael
author_sort Catania, Francesco
collection PubMed
description BACKGROUND: In protozoa, the identification of preserved motifs by comparative genomics is often impeded by difficulties to generate reliable alignments for non-coding sequences. Moreover, the evolutionary dynamics of regulatory elements in 3' untranslated regions (both in protozoa and metazoa) remains a virtually unexplored issue. RESULTS: By screening Paramecium tetraurelia's 3' untranslated regions for 8-mers that were previously found to be preserved in mammalian 3' UTRs, we detect and characterize a motif that is distinctly conserved in the ribosomal genes of this ciliate. The motif appears to be conserved across Paramecium aurelia species but is absent from the ribosomal genes of four additional non-Paramecium species surveyed, including another ciliate, Tetrahymena thermophila. Motif-free ribosomal genes retain fewer paralogs in the genome and appear to be lost more rapidly relative to motif-containing genes. Features associated with the discovered preserved motif are consistent with this 8-mer playing a role in post-transcriptional regulation. CONCLUSIONS: Our observations 1) shed light on the evolution of a putative regulatory motif across large phylogenetic distances; 2) are expected to facilitate the understanding of the modulation of ribosomal genes expression in Paramecium; and 3) reveal a largely unexplored--and presumably not restricted to Paramecium--association between the presence/absence of a DNA motif and the evolutionary fate of its host genes.
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spelling pubmed-28748012010-05-24 Evolutionary dynamics of a conserved sequence motif in the ribosomal genes of the ciliate Paramecium Catania, Francesco Lynch, Michael BMC Evol Biol Research article BACKGROUND: In protozoa, the identification of preserved motifs by comparative genomics is often impeded by difficulties to generate reliable alignments for non-coding sequences. Moreover, the evolutionary dynamics of regulatory elements in 3' untranslated regions (both in protozoa and metazoa) remains a virtually unexplored issue. RESULTS: By screening Paramecium tetraurelia's 3' untranslated regions for 8-mers that were previously found to be preserved in mammalian 3' UTRs, we detect and characterize a motif that is distinctly conserved in the ribosomal genes of this ciliate. The motif appears to be conserved across Paramecium aurelia species but is absent from the ribosomal genes of four additional non-Paramecium species surveyed, including another ciliate, Tetrahymena thermophila. Motif-free ribosomal genes retain fewer paralogs in the genome and appear to be lost more rapidly relative to motif-containing genes. Features associated with the discovered preserved motif are consistent with this 8-mer playing a role in post-transcriptional regulation. CONCLUSIONS: Our observations 1) shed light on the evolution of a putative regulatory motif across large phylogenetic distances; 2) are expected to facilitate the understanding of the modulation of ribosomal genes expression in Paramecium; and 3) reveal a largely unexplored--and presumably not restricted to Paramecium--association between the presence/absence of a DNA motif and the evolutionary fate of its host genes. BioMed Central 2010-05-04 /pmc/articles/PMC2874801/ /pubmed/20441586 http://dx.doi.org/10.1186/1471-2148-10-129 Text en Copyright ©2010 Catania and Lynch; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Catania, Francesco
Lynch, Michael
Evolutionary dynamics of a conserved sequence motif in the ribosomal genes of the ciliate Paramecium
title Evolutionary dynamics of a conserved sequence motif in the ribosomal genes of the ciliate Paramecium
title_full Evolutionary dynamics of a conserved sequence motif in the ribosomal genes of the ciliate Paramecium
title_fullStr Evolutionary dynamics of a conserved sequence motif in the ribosomal genes of the ciliate Paramecium
title_full_unstemmed Evolutionary dynamics of a conserved sequence motif in the ribosomal genes of the ciliate Paramecium
title_short Evolutionary dynamics of a conserved sequence motif in the ribosomal genes of the ciliate Paramecium
title_sort evolutionary dynamics of a conserved sequence motif in the ribosomal genes of the ciliate paramecium
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874801/
https://www.ncbi.nlm.nih.gov/pubmed/20441586
http://dx.doi.org/10.1186/1471-2148-10-129
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