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Modifiers of the Genotype–Phenotype Map: Hsp90 and Beyond

Disruption of certain genes alters the heritable phenotypic variation among individuals. Research on the chaperone Hsp90 has played a central role in determining the genetic basis of this phenomenon, which may be important to evolution and disease. Key studies have shown that Hsp90 perturbation modi...

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Detalles Bibliográficos
Autores principales: Schell, Rachel, Mullis, Martin, Ehrenreich, Ian M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5104472/
https://www.ncbi.nlm.nih.gov/pubmed/27832066
http://dx.doi.org/10.1371/journal.pbio.2001015
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author Schell, Rachel
Mullis, Martin
Ehrenreich, Ian M.
author_facet Schell, Rachel
Mullis, Martin
Ehrenreich, Ian M.
author_sort Schell, Rachel
collection PubMed
description Disruption of certain genes alters the heritable phenotypic variation among individuals. Research on the chaperone Hsp90 has played a central role in determining the genetic basis of this phenomenon, which may be important to evolution and disease. Key studies have shown that Hsp90 perturbation modifies the effects of many genetic variants throughout the genome. These modifications collectively transform the genotype–phenotype map, often resulting in a net increase or decrease in heritable phenotypic variation. Here, we summarize some of the foundational work on Hsp90 that led to these insights, discuss a framework for interpreting this research that is centered upon the standard genetics concept of epistasis, and propose major questions that future studies in this area should address.
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spelling pubmed-51044722016-12-08 Modifiers of the Genotype–Phenotype Map: Hsp90 and Beyond Schell, Rachel Mullis, Martin Ehrenreich, Ian M. PLoS Biol Primer Disruption of certain genes alters the heritable phenotypic variation among individuals. Research on the chaperone Hsp90 has played a central role in determining the genetic basis of this phenomenon, which may be important to evolution and disease. Key studies have shown that Hsp90 perturbation modifies the effects of many genetic variants throughout the genome. These modifications collectively transform the genotype–phenotype map, often resulting in a net increase or decrease in heritable phenotypic variation. Here, we summarize some of the foundational work on Hsp90 that led to these insights, discuss a framework for interpreting this research that is centered upon the standard genetics concept of epistasis, and propose major questions that future studies in this area should address. Public Library of Science 2016-11-10 /pmc/articles/PMC5104472/ /pubmed/27832066 http://dx.doi.org/10.1371/journal.pbio.2001015 Text en © 2016 Schell 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Primer
Schell, Rachel
Mullis, Martin
Ehrenreich, Ian M.
Modifiers of the Genotype–Phenotype Map: Hsp90 and Beyond
title Modifiers of the Genotype–Phenotype Map: Hsp90 and Beyond
title_full Modifiers of the Genotype–Phenotype Map: Hsp90 and Beyond
title_fullStr Modifiers of the Genotype–Phenotype Map: Hsp90 and Beyond
title_full_unstemmed Modifiers of the Genotype–Phenotype Map: Hsp90 and Beyond
title_short Modifiers of the Genotype–Phenotype Map: Hsp90 and Beyond
title_sort modifiers of the genotype–phenotype map: hsp90 and beyond
topic Primer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5104472/
https://www.ncbi.nlm.nih.gov/pubmed/27832066
http://dx.doi.org/10.1371/journal.pbio.2001015
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