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Idiosyncratic and dose-dependent epistasis drives variation in tomato fruit size
Epistasis between genes is traditionally studied using mutations that eliminate protein activity, but most natural genetic variation is in cis-regulatory DNA and influences gene expression and function quantitatively. Here, we use natural and engineered cis-regulatory alleles in a plant stem cell ci...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602613/ https://www.ncbi.nlm.nih.gov/pubmed/37856609 http://dx.doi.org/10.1126/science.adi5222 |
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author | Aguirre, Lyndsey Hendelman, Anat Hutton, Samuel F. McCandlish, David M. Lippman, Zachary B. |
author_facet | Aguirre, Lyndsey Hendelman, Anat Hutton, Samuel F. McCandlish, David M. Lippman, Zachary B. |
author_sort | Aguirre, Lyndsey |
collection | PubMed |
description | Epistasis between genes is traditionally studied using mutations that eliminate protein activity, but most natural genetic variation is in cis-regulatory DNA and influences gene expression and function quantitatively. Here, we use natural and engineered cis-regulatory alleles in a plant stem cell circuit to systematically evaluate epistatic relationships controlling tomato fruit size. Combining a promoter allelic series with two other loci, we collected over 30,000 phenotypic data points from 46 genotypes to quantify how allele strength transforms epistasis. We revealed a saturating dose-dependent relationship, but also allele-specific idiosyncratic interactions, including between alleles driving a step change in fruit size during domestication. Our approach and findings expose an underexplored dimension of epistasis, where cis-regulatory allelic diversity within gene regulatory networks elicits non-linear, unpredictable interactions that shape phenotypes. |
format | Online Article Text |
id | pubmed-10602613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-106026132023-10-26 Idiosyncratic and dose-dependent epistasis drives variation in tomato fruit size Aguirre, Lyndsey Hendelman, Anat Hutton, Samuel F. McCandlish, David M. Lippman, Zachary B. Science Article Epistasis between genes is traditionally studied using mutations that eliminate protein activity, but most natural genetic variation is in cis-regulatory DNA and influences gene expression and function quantitatively. Here, we use natural and engineered cis-regulatory alleles in a plant stem cell circuit to systematically evaluate epistatic relationships controlling tomato fruit size. Combining a promoter allelic series with two other loci, we collected over 30,000 phenotypic data points from 46 genotypes to quantify how allele strength transforms epistasis. We revealed a saturating dose-dependent relationship, but also allele-specific idiosyncratic interactions, including between alleles driving a step change in fruit size during domestication. Our approach and findings expose an underexplored dimension of epistasis, where cis-regulatory allelic diversity within gene regulatory networks elicits non-linear, unpredictable interactions that shape phenotypes. 2023-10-20 2023-10-19 /pmc/articles/PMC10602613/ /pubmed/37856609 http://dx.doi.org/10.1126/science.adi5222 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License, which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Aguirre, Lyndsey Hendelman, Anat Hutton, Samuel F. McCandlish, David M. Lippman, Zachary B. Idiosyncratic and dose-dependent epistasis drives variation in tomato fruit size |
title | Idiosyncratic and dose-dependent epistasis drives variation in tomato fruit size |
title_full | Idiosyncratic and dose-dependent epistasis drives variation in tomato fruit size |
title_fullStr | Idiosyncratic and dose-dependent epistasis drives variation in tomato fruit size |
title_full_unstemmed | Idiosyncratic and dose-dependent epistasis drives variation in tomato fruit size |
title_short | Idiosyncratic and dose-dependent epistasis drives variation in tomato fruit size |
title_sort | idiosyncratic and dose-dependent epistasis drives variation in tomato fruit size |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602613/ https://www.ncbi.nlm.nih.gov/pubmed/37856609 http://dx.doi.org/10.1126/science.adi5222 |
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