Cargando…
Extent and context dependence of pleiotropy revealed by high-throughput single-cell phenotyping
Pleiotropy—when a single mutation affects multiple traits—is a controversial topic with far-reaching implications. Pleiotropy plays a central role in debates about how complex traits evolve and whether biological systems are modular or are organized such that every gene has the potential to affect m...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7451985/ https://www.ncbi.nlm.nih.gov/pubmed/32804946 http://dx.doi.org/10.1371/journal.pbio.3000836 |
_version_ | 1783575083948703744 |
---|---|
author | Geiler-Samerotte, Kerry A. Li, Shuang Lazaris, Charalampos Taylor, Austin Ziv, Naomi Ramjeawan, Chelsea Paaby, Annalise B. Siegal, Mark L. |
author_facet | Geiler-Samerotte, Kerry A. Li, Shuang Lazaris, Charalampos Taylor, Austin Ziv, Naomi Ramjeawan, Chelsea Paaby, Annalise B. Siegal, Mark L. |
author_sort | Geiler-Samerotte, Kerry A. |
collection | PubMed |
description | Pleiotropy—when a single mutation affects multiple traits—is a controversial topic with far-reaching implications. Pleiotropy plays a central role in debates about how complex traits evolve and whether biological systems are modular or are organized such that every gene has the potential to affect many traits. Pleiotropy is also critical to initiatives in evolutionary medicine that seek to trap infectious microbes or tumors by selecting for mutations that encourage growth in some conditions at the expense of others. Research in these fields, and others, would benefit from understanding the extent to which pleiotropy reflects inherent relationships among phenotypes that correlate no matter the perturbation (vertical pleiotropy). Alternatively, pleiotropy may result from genetic changes that impose correlations between otherwise independent traits (horizontal pleiotropy). We distinguish these possibilities by using clonal populations of yeast cells to quantify the inherent relationships between single-cell morphological features. Then, we demonstrate how often these relationships underlie vertical pleiotropy and how often these relationships are modified by genetic variants (quantitative trait loci [QTL]) acting via horizontal pleiotropy. Our comprehensive screen measures thousands of pairwise trait correlations across hundreds of thousands of yeast cells and reveals ample evidence of both vertical and horizontal pleiotropy. Additionally, we observe that the correlations between traits can change with the environment, genetic background, and cell-cycle position. These changing dependencies suggest a nuanced view of pleiotropy: biological systems demonstrate limited pleiotropy in any given context, but across contexts (e.g., across diverse environments and genetic backgrounds) each genetic change has the potential to influence a larger number of traits. Our method suggests that exploiting pleiotropy for applications in evolutionary medicine would benefit from focusing on traits with correlations that are less dependent on context. |
format | Online Article Text |
id | pubmed-7451985 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74519852020-09-02 Extent and context dependence of pleiotropy revealed by high-throughput single-cell phenotyping Geiler-Samerotte, Kerry A. Li, Shuang Lazaris, Charalampos Taylor, Austin Ziv, Naomi Ramjeawan, Chelsea Paaby, Annalise B. Siegal, Mark L. PLoS Biol Methods and Resources Pleiotropy—when a single mutation affects multiple traits—is a controversial topic with far-reaching implications. Pleiotropy plays a central role in debates about how complex traits evolve and whether biological systems are modular or are organized such that every gene has the potential to affect many traits. Pleiotropy is also critical to initiatives in evolutionary medicine that seek to trap infectious microbes or tumors by selecting for mutations that encourage growth in some conditions at the expense of others. Research in these fields, and others, would benefit from understanding the extent to which pleiotropy reflects inherent relationships among phenotypes that correlate no matter the perturbation (vertical pleiotropy). Alternatively, pleiotropy may result from genetic changes that impose correlations between otherwise independent traits (horizontal pleiotropy). We distinguish these possibilities by using clonal populations of yeast cells to quantify the inherent relationships between single-cell morphological features. Then, we demonstrate how often these relationships underlie vertical pleiotropy and how often these relationships are modified by genetic variants (quantitative trait loci [QTL]) acting via horizontal pleiotropy. Our comprehensive screen measures thousands of pairwise trait correlations across hundreds of thousands of yeast cells and reveals ample evidence of both vertical and horizontal pleiotropy. Additionally, we observe that the correlations between traits can change with the environment, genetic background, and cell-cycle position. These changing dependencies suggest a nuanced view of pleiotropy: biological systems demonstrate limited pleiotropy in any given context, but across contexts (e.g., across diverse environments and genetic backgrounds) each genetic change has the potential to influence a larger number of traits. Our method suggests that exploiting pleiotropy for applications in evolutionary medicine would benefit from focusing on traits with correlations that are less dependent on context. Public Library of Science 2020-08-17 /pmc/articles/PMC7451985/ /pubmed/32804946 http://dx.doi.org/10.1371/journal.pbio.3000836 Text en © 2020 Geiler-Samerotte 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 | Methods and Resources Geiler-Samerotte, Kerry A. Li, Shuang Lazaris, Charalampos Taylor, Austin Ziv, Naomi Ramjeawan, Chelsea Paaby, Annalise B. Siegal, Mark L. Extent and context dependence of pleiotropy revealed by high-throughput single-cell phenotyping |
title | Extent and context dependence of pleiotropy revealed by high-throughput single-cell phenotyping |
title_full | Extent and context dependence of pleiotropy revealed by high-throughput single-cell phenotyping |
title_fullStr | Extent and context dependence of pleiotropy revealed by high-throughput single-cell phenotyping |
title_full_unstemmed | Extent and context dependence of pleiotropy revealed by high-throughput single-cell phenotyping |
title_short | Extent and context dependence of pleiotropy revealed by high-throughput single-cell phenotyping |
title_sort | extent and context dependence of pleiotropy revealed by high-throughput single-cell phenotyping |
topic | Methods and Resources |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7451985/ https://www.ncbi.nlm.nih.gov/pubmed/32804946 http://dx.doi.org/10.1371/journal.pbio.3000836 |
work_keys_str_mv | AT geilersamerottekerrya extentandcontextdependenceofpleiotropyrevealedbyhighthroughputsinglecellphenotyping AT lishuang extentandcontextdependenceofpleiotropyrevealedbyhighthroughputsinglecellphenotyping AT lazarischaralampos extentandcontextdependenceofpleiotropyrevealedbyhighthroughputsinglecellphenotyping AT tayloraustin extentandcontextdependenceofpleiotropyrevealedbyhighthroughputsinglecellphenotyping AT zivnaomi extentandcontextdependenceofpleiotropyrevealedbyhighthroughputsinglecellphenotyping AT ramjeawanchelsea extentandcontextdependenceofpleiotropyrevealedbyhighthroughputsinglecellphenotyping AT paabyannaliseb extentandcontextdependenceofpleiotropyrevealedbyhighthroughputsinglecellphenotyping AT siegalmarkl extentandcontextdependenceofpleiotropyrevealedbyhighthroughputsinglecellphenotyping |