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Accurate Simulation and Detection of Coevolution Signals in Multiple Sequence Alignments

BACKGROUND: While the conserved positions of a multiple sequence alignment (MSA) are clearly of interest, non-conserved positions can also be important because, for example, destabilizing effects at one position can be compensated by stabilizing effects at another position. Different methods have be...

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Autores principales: Ackerman, Sharon H., Tillier, Elisabeth R., Gatti, Domenico L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3473043/
https://www.ncbi.nlm.nih.gov/pubmed/23091608
http://dx.doi.org/10.1371/journal.pone.0047108
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author Ackerman, Sharon H.
Tillier, Elisabeth R.
Gatti, Domenico L.
author_facet Ackerman, Sharon H.
Tillier, Elisabeth R.
Gatti, Domenico L.
author_sort Ackerman, Sharon H.
collection PubMed
description BACKGROUND: While the conserved positions of a multiple sequence alignment (MSA) are clearly of interest, non-conserved positions can also be important because, for example, destabilizing effects at one position can be compensated by stabilizing effects at another position. Different methods have been developed to recognize the evolutionary relationship between amino acid sites, and to disentangle functional/structural dependencies from historical/phylogenetic ones. METHODOLOGY/PRINCIPAL FINDINGS: We have used two complementary approaches to test the efficacy of these methods. In the first approach, we have used a new program, MSAvolve, for the in silico evolution of MSAs, which records a detailed history of all covarying positions, and builds a global coevolution matrix as the accumulated sum of individual matrices for the positions forced to co-vary, the recombinant coevolution, and the stochastic coevolution. We have simulated over 1600 MSAs for 8 protein families, which reflect sequences of different sizes and proteins with widely different functions. The calculated coevolution matrices were compared with the coevolution matrices obtained for the same evolved MSAs with different coevolution detection methods. In a second approach we have evaluated the capacity of the different methods to predict close contacts in the representative X-ray structures of an additional 150 protein families using only experimental MSAs. CONCLUSIONS/SIGNIFICANCE: Methods based on the identification of global correlations between pairs were found to be generally superior to methods based only on local correlations in their capacity to identify coevolving residues using either simulated or experimental MSAs. However, the significant variability in the performance of different methods with different proteins suggests that the simulation of MSAs that replicate the statistical properties of the experimental MSA can be a valuable tool to identify the coevolution detection method that is most effective in each case.
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spelling pubmed-34730432012-10-22 Accurate Simulation and Detection of Coevolution Signals in Multiple Sequence Alignments Ackerman, Sharon H. Tillier, Elisabeth R. Gatti, Domenico L. PLoS One Research Article BACKGROUND: While the conserved positions of a multiple sequence alignment (MSA) are clearly of interest, non-conserved positions can also be important because, for example, destabilizing effects at one position can be compensated by stabilizing effects at another position. Different methods have been developed to recognize the evolutionary relationship between amino acid sites, and to disentangle functional/structural dependencies from historical/phylogenetic ones. METHODOLOGY/PRINCIPAL FINDINGS: We have used two complementary approaches to test the efficacy of these methods. In the first approach, we have used a new program, MSAvolve, for the in silico evolution of MSAs, which records a detailed history of all covarying positions, and builds a global coevolution matrix as the accumulated sum of individual matrices for the positions forced to co-vary, the recombinant coevolution, and the stochastic coevolution. We have simulated over 1600 MSAs for 8 protein families, which reflect sequences of different sizes and proteins with widely different functions. The calculated coevolution matrices were compared with the coevolution matrices obtained for the same evolved MSAs with different coevolution detection methods. In a second approach we have evaluated the capacity of the different methods to predict close contacts in the representative X-ray structures of an additional 150 protein families using only experimental MSAs. CONCLUSIONS/SIGNIFICANCE: Methods based on the identification of global correlations between pairs were found to be generally superior to methods based only on local correlations in their capacity to identify coevolving residues using either simulated or experimental MSAs. However, the significant variability in the performance of different methods with different proteins suggests that the simulation of MSAs that replicate the statistical properties of the experimental MSA can be a valuable tool to identify the coevolution detection method that is most effective in each case. Public Library of Science 2012-10-16 /pmc/articles/PMC3473043/ /pubmed/23091608 http://dx.doi.org/10.1371/journal.pone.0047108 Text en © 2012 Ackerman 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
Ackerman, Sharon H.
Tillier, Elisabeth R.
Gatti, Domenico L.
Accurate Simulation and Detection of Coevolution Signals in Multiple Sequence Alignments
title Accurate Simulation and Detection of Coevolution Signals in Multiple Sequence Alignments
title_full Accurate Simulation and Detection of Coevolution Signals in Multiple Sequence Alignments
title_fullStr Accurate Simulation and Detection of Coevolution Signals in Multiple Sequence Alignments
title_full_unstemmed Accurate Simulation and Detection of Coevolution Signals in Multiple Sequence Alignments
title_short Accurate Simulation and Detection of Coevolution Signals in Multiple Sequence Alignments
title_sort accurate simulation and detection of coevolution signals in multiple sequence alignments
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3473043/
https://www.ncbi.nlm.nih.gov/pubmed/23091608
http://dx.doi.org/10.1371/journal.pone.0047108
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