Cargando…

The Genotype–Phenotype Relationships in the Light of Natural Selection

Although any genotype–phenotype relationships are a result of evolution, little is known about how natural selection and neutral drift, two distinct driving forces of evolution, operate to shape the relationships. By analyzing ∼500 yeast quantitative traits, we reveal a basic “supervisor–worker” gen...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Han, Wu, Chung-I, He, Xionglei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850688/
https://www.ncbi.nlm.nih.gov/pubmed/29136190
http://dx.doi.org/10.1093/molbev/msx288
_version_ 1783306266695696384
author Chen, Han
Wu, Chung-I
He, Xionglei
author_facet Chen, Han
Wu, Chung-I
He, Xionglei
author_sort Chen, Han
collection PubMed
description Although any genotype–phenotype relationships are a result of evolution, little is known about how natural selection and neutral drift, two distinct driving forces of evolution, operate to shape the relationships. By analyzing ∼500 yeast quantitative traits, we reveal a basic “supervisor–worker” gene architecture underlying a trait. Supervisors are often identified by “perturbational” approaches (such as gene deletion), whereas workers, which usually show small and statistically insignificant deletion effects, are tracked primarily by “observational” approaches that examine the correlation between gene activity and trait value across a number of conditions. Accordingly, supervisors provide most of the genetic understandings of the trait whereas workers provide rich mechanistic understandings. Further analyses suggest that most observed supervisor–worker interactions may evolve largely neutrally, resulting in pervasive between-worker epistasis that suppresses the tractability of workers. In contrast, a fraction of supervisors are recruited/maintained by natural selection to build worker co-expression, boosting the tractability of workers. Thus, by revealing a supervisor–worker gene architecture underlying complex traits, the opposite roles of natural selection versus neutral drift in shaping the gene architecture, and the complementary strengths of the perturbational and observational research strategies in characterizing the gene architecture, this study may lay a new conceptual foundation for understanding the molecular basis of complex traits.
format Online
Article
Text
id pubmed-5850688
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-58506882018-03-23 The Genotype–Phenotype Relationships in the Light of Natural Selection Chen, Han Wu, Chung-I He, Xionglei Mol Biol Evol Fast Track Although any genotype–phenotype relationships are a result of evolution, little is known about how natural selection and neutral drift, two distinct driving forces of evolution, operate to shape the relationships. By analyzing ∼500 yeast quantitative traits, we reveal a basic “supervisor–worker” gene architecture underlying a trait. Supervisors are often identified by “perturbational” approaches (such as gene deletion), whereas workers, which usually show small and statistically insignificant deletion effects, are tracked primarily by “observational” approaches that examine the correlation between gene activity and trait value across a number of conditions. Accordingly, supervisors provide most of the genetic understandings of the trait whereas workers provide rich mechanistic understandings. Further analyses suggest that most observed supervisor–worker interactions may evolve largely neutrally, resulting in pervasive between-worker epistasis that suppresses the tractability of workers. In contrast, a fraction of supervisors are recruited/maintained by natural selection to build worker co-expression, boosting the tractability of workers. Thus, by revealing a supervisor–worker gene architecture underlying complex traits, the opposite roles of natural selection versus neutral drift in shaping the gene architecture, and the complementary strengths of the perturbational and observational research strategies in characterizing the gene architecture, this study may lay a new conceptual foundation for understanding the molecular basis of complex traits. Oxford University Press 2018-03 2017-11-09 /pmc/articles/PMC5850688/ /pubmed/29136190 http://dx.doi.org/10.1093/molbev/msx288 Text en © The Author 2017. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Fast Track
Chen, Han
Wu, Chung-I
He, Xionglei
The Genotype–Phenotype Relationships in the Light of Natural Selection
title The Genotype–Phenotype Relationships in the Light of Natural Selection
title_full The Genotype–Phenotype Relationships in the Light of Natural Selection
title_fullStr The Genotype–Phenotype Relationships in the Light of Natural Selection
title_full_unstemmed The Genotype–Phenotype Relationships in the Light of Natural Selection
title_short The Genotype–Phenotype Relationships in the Light of Natural Selection
title_sort genotype–phenotype relationships in the light of natural selection
topic Fast Track
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850688/
https://www.ncbi.nlm.nih.gov/pubmed/29136190
http://dx.doi.org/10.1093/molbev/msx288
work_keys_str_mv AT chenhan thegenotypephenotyperelationshipsinthelightofnaturalselection
AT wuchungi thegenotypephenotyperelationshipsinthelightofnaturalselection
AT hexionglei thegenotypephenotyperelationshipsinthelightofnaturalselection
AT chenhan genotypephenotyperelationshipsinthelightofnaturalselection
AT wuchungi genotypephenotyperelationshipsinthelightofnaturalselection
AT hexionglei genotypephenotyperelationshipsinthelightofnaturalselection