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Inactivity periods and postural change speed can explain atypical postural change patterns of Caenorhabditis elegans mutants
BACKGROUND: With rapid advances in genome sequencing and editing technologies, systematic and quantitative analysis of animal behavior is expected to be another key to facilitating data-driven behavioral genetics. The nematode Caenorhabditis elegans is a model organism in this field. Several video-t...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244558/ https://www.ncbi.nlm.nih.gov/pubmed/28103804 http://dx.doi.org/10.1186/s12859-016-1408-8 |
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author | Fukunaga, Tsukasa Iwasaki, Wataru |
author_facet | Fukunaga, Tsukasa Iwasaki, Wataru |
author_sort | Fukunaga, Tsukasa |
collection | PubMed |
description | BACKGROUND: With rapid advances in genome sequencing and editing technologies, systematic and quantitative analysis of animal behavior is expected to be another key to facilitating data-driven behavioral genetics. The nematode Caenorhabditis elegans is a model organism in this field. Several video-tracking systems are available for automatically recording behavioral data for the nematode, but computational methods for analyzing these data are still under development. RESULTS: In this study, we applied the Gaussian mixture model-based binning method to time-series postural data for 322 C. elegans strains. We revealed that the occurrence patterns of the postural states and the transition patterns among these states have a relationship as expected, and such a relationship must be taken into account to identify strains with atypical behaviors that are different from those of wild type. Based on this observation, we identified several strains that exhibit atypical transition patterns that cannot be fully explained by their occurrence patterns of postural states. Surprisingly, we found that two simple factors—overall acceleration of postural movement and elimination of inactivity periods—explained the behavioral characteristics of strains with very atypical transition patterns; therefore, computational analysis of animal behavior must be accompanied by evaluation of the effects of these simple factors. Finally, we found that the npr-1 and npr-3 mutants have similar behavioral patterns that were not predictable by sequence homology, proving that our data-driven approach can reveal the functions of genes that have not yet been characterized. CONCLUSION: We propose that elimination of inactivity periods and overall acceleration of postural change speed can explain behavioral phenotypes of strains with very atypical postural transition patterns. Our methods and results constitute guidelines for effectively finding strains that show “truly” interesting behaviors and systematically uncovering novel gene functions by bioimage-informatic approaches. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-1408-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5244558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52445582017-01-23 Inactivity periods and postural change speed can explain atypical postural change patterns of Caenorhabditis elegans mutants Fukunaga, Tsukasa Iwasaki, Wataru BMC Bioinformatics Research Article BACKGROUND: With rapid advances in genome sequencing and editing technologies, systematic and quantitative analysis of animal behavior is expected to be another key to facilitating data-driven behavioral genetics. The nematode Caenorhabditis elegans is a model organism in this field. Several video-tracking systems are available for automatically recording behavioral data for the nematode, but computational methods for analyzing these data are still under development. RESULTS: In this study, we applied the Gaussian mixture model-based binning method to time-series postural data for 322 C. elegans strains. We revealed that the occurrence patterns of the postural states and the transition patterns among these states have a relationship as expected, and such a relationship must be taken into account to identify strains with atypical behaviors that are different from those of wild type. Based on this observation, we identified several strains that exhibit atypical transition patterns that cannot be fully explained by their occurrence patterns of postural states. Surprisingly, we found that two simple factors—overall acceleration of postural movement and elimination of inactivity periods—explained the behavioral characteristics of strains with very atypical transition patterns; therefore, computational analysis of animal behavior must be accompanied by evaluation of the effects of these simple factors. Finally, we found that the npr-1 and npr-3 mutants have similar behavioral patterns that were not predictable by sequence homology, proving that our data-driven approach can reveal the functions of genes that have not yet been characterized. CONCLUSION: We propose that elimination of inactivity periods and overall acceleration of postural change speed can explain behavioral phenotypes of strains with very atypical postural transition patterns. Our methods and results constitute guidelines for effectively finding strains that show “truly” interesting behaviors and systematically uncovering novel gene functions by bioimage-informatic approaches. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-1408-8) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-19 /pmc/articles/PMC5244558/ /pubmed/28103804 http://dx.doi.org/10.1186/s12859-016-1408-8 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License(http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Fukunaga, Tsukasa Iwasaki, Wataru Inactivity periods and postural change speed can explain atypical postural change patterns of Caenorhabditis elegans mutants |
title | Inactivity periods and postural change speed can explain atypical postural change patterns of Caenorhabditis elegans mutants |
title_full | Inactivity periods and postural change speed can explain atypical postural change patterns of Caenorhabditis elegans mutants |
title_fullStr | Inactivity periods and postural change speed can explain atypical postural change patterns of Caenorhabditis elegans mutants |
title_full_unstemmed | Inactivity periods and postural change speed can explain atypical postural change patterns of Caenorhabditis elegans mutants |
title_short | Inactivity periods and postural change speed can explain atypical postural change patterns of Caenorhabditis elegans mutants |
title_sort | inactivity periods and postural change speed can explain atypical postural change patterns of caenorhabditis elegans mutants |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244558/ https://www.ncbi.nlm.nih.gov/pubmed/28103804 http://dx.doi.org/10.1186/s12859-016-1408-8 |
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