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Neighborhood Properties Are Important Determinants of Temperature Sensitive Mutations

Temperature-sensitive (TS) mutants are powerful tools to study gene function in vivo. These mutants exhibit wild-type activity at permissive temperatures and reduced activity at restrictive temperatures. Although random mutagenesis can be used to generate TS mutants, the procedure is laborious and u...

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Autores principales: Lockwood, Svetlana, Krishnamoorthy, Bala, Ye, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3229608/
https://www.ncbi.nlm.nih.gov/pubmed/22164302
http://dx.doi.org/10.1371/journal.pone.0028507
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author Lockwood, Svetlana
Krishnamoorthy, Bala
Ye, Ping
author_facet Lockwood, Svetlana
Krishnamoorthy, Bala
Ye, Ping
author_sort Lockwood, Svetlana
collection PubMed
description Temperature-sensitive (TS) mutants are powerful tools to study gene function in vivo. These mutants exhibit wild-type activity at permissive temperatures and reduced activity at restrictive temperatures. Although random mutagenesis can be used to generate TS mutants, the procedure is laborious and unfeasible in multicellular organisms. Further, the underlying molecular mechanisms of the TS phenotype are poorly understood. To elucidate TS mechanisms, we used a machine learning method–logistic regression–to investigate a large number of sequence and structure features. We developed and tested 133 features, describing properties of either the mutation site or the mutation site neighborhood. We defined three types of neighborhood using sequence distance, Euclidean distance, and topological distance. We discovered that neighborhood features outperformed mutation site features in predicting TS mutations. The most predictive features suggest that TS mutations tend to occur at buried and rigid residues, and are located at conserved protein domains. The environment of a buried residue often determines the overall structural stability of a protein, thus may lead to reversible activity change upon temperature switch. We developed TS prediction models based on logistic regression and the Lasso regularized procedure. Through a ten-fold cross-validation, we obtained the area under the curve of 0.91 for the model using both sequence and structure features. Testing on independent datasets suggested that the model predicted TS mutations with a 50% precision. In summary, our study elucidated the molecular basis of TS mutants and suggested the importance of neighborhood properties in determining TS mutations. We further developed models to predict TS mutations derived from single amino acid substitutions. In this way, TS mutants can be efficiently obtained through experimentally introducing the predicted mutations.
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spelling pubmed-32296082011-12-07 Neighborhood Properties Are Important Determinants of Temperature Sensitive Mutations Lockwood, Svetlana Krishnamoorthy, Bala Ye, Ping PLoS One Research Article Temperature-sensitive (TS) mutants are powerful tools to study gene function in vivo. These mutants exhibit wild-type activity at permissive temperatures and reduced activity at restrictive temperatures. Although random mutagenesis can be used to generate TS mutants, the procedure is laborious and unfeasible in multicellular organisms. Further, the underlying molecular mechanisms of the TS phenotype are poorly understood. To elucidate TS mechanisms, we used a machine learning method–logistic regression–to investigate a large number of sequence and structure features. We developed and tested 133 features, describing properties of either the mutation site or the mutation site neighborhood. We defined three types of neighborhood using sequence distance, Euclidean distance, and topological distance. We discovered that neighborhood features outperformed mutation site features in predicting TS mutations. The most predictive features suggest that TS mutations tend to occur at buried and rigid residues, and are located at conserved protein domains. The environment of a buried residue often determines the overall structural stability of a protein, thus may lead to reversible activity change upon temperature switch. We developed TS prediction models based on logistic regression and the Lasso regularized procedure. Through a ten-fold cross-validation, we obtained the area under the curve of 0.91 for the model using both sequence and structure features. Testing on independent datasets suggested that the model predicted TS mutations with a 50% precision. In summary, our study elucidated the molecular basis of TS mutants and suggested the importance of neighborhood properties in determining TS mutations. We further developed models to predict TS mutations derived from single amino acid substitutions. In this way, TS mutants can be efficiently obtained through experimentally introducing the predicted mutations. Public Library of Science 2011-12-02 /pmc/articles/PMC3229608/ /pubmed/22164302 http://dx.doi.org/10.1371/journal.pone.0028507 Text en Lockwood 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
Lockwood, Svetlana
Krishnamoorthy, Bala
Ye, Ping
Neighborhood Properties Are Important Determinants of Temperature Sensitive Mutations
title Neighborhood Properties Are Important Determinants of Temperature Sensitive Mutations
title_full Neighborhood Properties Are Important Determinants of Temperature Sensitive Mutations
title_fullStr Neighborhood Properties Are Important Determinants of Temperature Sensitive Mutations
title_full_unstemmed Neighborhood Properties Are Important Determinants of Temperature Sensitive Mutations
title_short Neighborhood Properties Are Important Determinants of Temperature Sensitive Mutations
title_sort neighborhood properties are important determinants of temperature sensitive mutations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3229608/
https://www.ncbi.nlm.nih.gov/pubmed/22164302
http://dx.doi.org/10.1371/journal.pone.0028507
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