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Variable paralog expression underlies phenotype variation

Human faces are variable; we look different from one another. Craniofacial disorders further increase facial variation. To understand craniofacial variation and how it can be buffered, we analyzed the zebrafish mef2ca mutant. When this transcription factor encoding gene is mutated, zebrafish develop...

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Autores principales: Bailon-Zambrano, Raisa, Sucharov, Juliana, Mumme-Monheit, Abigail, Murry, Matthew, Stenzel, Amanda, Pulvino, Anthony T, Mitchell, Jennyfer M, Colborn, Kathryn L, Nichols, James T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555865/
https://www.ncbi.nlm.nih.gov/pubmed/36134886
http://dx.doi.org/10.7554/eLife.79247
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author Bailon-Zambrano, Raisa
Sucharov, Juliana
Mumme-Monheit, Abigail
Murry, Matthew
Stenzel, Amanda
Pulvino, Anthony T
Mitchell, Jennyfer M
Colborn, Kathryn L
Nichols, James T
author_facet Bailon-Zambrano, Raisa
Sucharov, Juliana
Mumme-Monheit, Abigail
Murry, Matthew
Stenzel, Amanda
Pulvino, Anthony T
Mitchell, Jennyfer M
Colborn, Kathryn L
Nichols, James T
author_sort Bailon-Zambrano, Raisa
collection PubMed
description Human faces are variable; we look different from one another. Craniofacial disorders further increase facial variation. To understand craniofacial variation and how it can be buffered, we analyzed the zebrafish mef2ca mutant. When this transcription factor encoding gene is mutated, zebrafish develop dramatically variable craniofacial phenotypes. Years of selective breeding for low and high penetrance of mutant phenotypes produced strains that are either resilient or sensitive to the mef2ca mutation. Here, we compared gene expression between these strains, which revealed that selective breeding enriched for high and low mef2ca paralog expression in the low- and high-penetrance strains, respectively. We found that mef2ca paralog expression is variable in unselected wild-type zebrafish, motivating the hypothesis that heritable variation in paralog expression underlies mutant phenotype severity and variation. In support, mutagenizing the mef2ca paralogs, mef2aa, mef2b, mef2cb, and mef2d demonstrated modular buffering by paralogs. Specifically, some paralogs buffer severity while others buffer variability. We present a novel, mechanistic model for phenotypic variation where variable, vestigial paralog expression buffers development. These studies are a major step forward in understanding the mechanisms of facial variation, including how some genetically resilient individuals can overcome a deleterious mutation.
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spelling pubmed-95558652022-10-13 Variable paralog expression underlies phenotype variation Bailon-Zambrano, Raisa Sucharov, Juliana Mumme-Monheit, Abigail Murry, Matthew Stenzel, Amanda Pulvino, Anthony T Mitchell, Jennyfer M Colborn, Kathryn L Nichols, James T eLife Developmental Biology Human faces are variable; we look different from one another. Craniofacial disorders further increase facial variation. To understand craniofacial variation and how it can be buffered, we analyzed the zebrafish mef2ca mutant. When this transcription factor encoding gene is mutated, zebrafish develop dramatically variable craniofacial phenotypes. Years of selective breeding for low and high penetrance of mutant phenotypes produced strains that are either resilient or sensitive to the mef2ca mutation. Here, we compared gene expression between these strains, which revealed that selective breeding enriched for high and low mef2ca paralog expression in the low- and high-penetrance strains, respectively. We found that mef2ca paralog expression is variable in unselected wild-type zebrafish, motivating the hypothesis that heritable variation in paralog expression underlies mutant phenotype severity and variation. In support, mutagenizing the mef2ca paralogs, mef2aa, mef2b, mef2cb, and mef2d demonstrated modular buffering by paralogs. Specifically, some paralogs buffer severity while others buffer variability. We present a novel, mechanistic model for phenotypic variation where variable, vestigial paralog expression buffers development. These studies are a major step forward in understanding the mechanisms of facial variation, including how some genetically resilient individuals can overcome a deleterious mutation. eLife Sciences Publications, Ltd 2022-09-22 /pmc/articles/PMC9555865/ /pubmed/36134886 http://dx.doi.org/10.7554/eLife.79247 Text en © 2022, Bailon-Zambrano, Sucharov et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Bailon-Zambrano, Raisa
Sucharov, Juliana
Mumme-Monheit, Abigail
Murry, Matthew
Stenzel, Amanda
Pulvino, Anthony T
Mitchell, Jennyfer M
Colborn, Kathryn L
Nichols, James T
Variable paralog expression underlies phenotype variation
title Variable paralog expression underlies phenotype variation
title_full Variable paralog expression underlies phenotype variation
title_fullStr Variable paralog expression underlies phenotype variation
title_full_unstemmed Variable paralog expression underlies phenotype variation
title_short Variable paralog expression underlies phenotype variation
title_sort variable paralog expression underlies phenotype variation
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555865/
https://www.ncbi.nlm.nih.gov/pubmed/36134886
http://dx.doi.org/10.7554/eLife.79247
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