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Regulatory Architecture of Gene Expression Variation in the Threespine Stickleback Gasterosteus aculeatus

Much adaptive evolutionary change is underlain by mutational variation in regions of the genome that regulate gene expression rather than in the coding regions of the genes themselves. An understanding of the role of gene expression variation in facilitating local adaptation will be aided by an unde...

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Autores principales: Pritchard, Victoria L., Viitaniemi, Heidi M., McCairns, R. J. Scott, Merilä, Juha, Nikinmaa, Mikko, Primmer, Craig R., Leder, Erica H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217106/
https://www.ncbi.nlm.nih.gov/pubmed/27836907
http://dx.doi.org/10.1534/g3.116.033241
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author Pritchard, Victoria L.
Viitaniemi, Heidi M.
McCairns, R. J. Scott
Merilä, Juha
Nikinmaa, Mikko
Primmer, Craig R.
Leder, Erica H.
author_facet Pritchard, Victoria L.
Viitaniemi, Heidi M.
McCairns, R. J. Scott
Merilä, Juha
Nikinmaa, Mikko
Primmer, Craig R.
Leder, Erica H.
author_sort Pritchard, Victoria L.
collection PubMed
description Much adaptive evolutionary change is underlain by mutational variation in regions of the genome that regulate gene expression rather than in the coding regions of the genes themselves. An understanding of the role of gene expression variation in facilitating local adaptation will be aided by an understanding of underlying regulatory networks. Here, we characterize the genetic architecture of gene expression variation in the threespine stickleback (Gasterosteus aculeatus), an important model in the study of adaptive evolution. We collected transcriptomic and genomic data from 60 half-sib families using an expression microarray and genotyping-by-sequencing, and located expression quantitative trait loci (eQTL) underlying the variation in gene expression in liver tissue using an interval mapping approach. We identified eQTL for several thousand expression traits. Expression was influenced by polymorphism in both cis- and trans-regulatory regions. Trans-eQTL clustered into hotspots. We did not identify master transcriptional regulators in hotspot locations: rather, the presence of hotspots may be driven by complex interactions between multiple transcription factors. One observed hotspot colocated with a QTL recently found to underlie salinity tolerance in the threespine stickleback. However, most other observed hotspots did not colocate with regions of the genome known to be involved in adaptive divergence between marine and freshwater habitats.
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spelling pubmed-52171062017-01-09 Regulatory Architecture of Gene Expression Variation in the Threespine Stickleback Gasterosteus aculeatus Pritchard, Victoria L. Viitaniemi, Heidi M. McCairns, R. J. Scott Merilä, Juha Nikinmaa, Mikko Primmer, Craig R. Leder, Erica H. G3 (Bethesda) Investigations Much adaptive evolutionary change is underlain by mutational variation in regions of the genome that regulate gene expression rather than in the coding regions of the genes themselves. An understanding of the role of gene expression variation in facilitating local adaptation will be aided by an understanding of underlying regulatory networks. Here, we characterize the genetic architecture of gene expression variation in the threespine stickleback (Gasterosteus aculeatus), an important model in the study of adaptive evolution. We collected transcriptomic and genomic data from 60 half-sib families using an expression microarray and genotyping-by-sequencing, and located expression quantitative trait loci (eQTL) underlying the variation in gene expression in liver tissue using an interval mapping approach. We identified eQTL for several thousand expression traits. Expression was influenced by polymorphism in both cis- and trans-regulatory regions. Trans-eQTL clustered into hotspots. We did not identify master transcriptional regulators in hotspot locations: rather, the presence of hotspots may be driven by complex interactions between multiple transcription factors. One observed hotspot colocated with a QTL recently found to underlie salinity tolerance in the threespine stickleback. However, most other observed hotspots did not colocate with regions of the genome known to be involved in adaptive divergence between marine and freshwater habitats. Genetics Society of America 2016-11-10 /pmc/articles/PMC5217106/ /pubmed/27836907 http://dx.doi.org/10.1534/g3.116.033241 Text en Copyright © 2017 Pritchard et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Pritchard, Victoria L.
Viitaniemi, Heidi M.
McCairns, R. J. Scott
Merilä, Juha
Nikinmaa, Mikko
Primmer, Craig R.
Leder, Erica H.
Regulatory Architecture of Gene Expression Variation in the Threespine Stickleback Gasterosteus aculeatus
title Regulatory Architecture of Gene Expression Variation in the Threespine Stickleback Gasterosteus aculeatus
title_full Regulatory Architecture of Gene Expression Variation in the Threespine Stickleback Gasterosteus aculeatus
title_fullStr Regulatory Architecture of Gene Expression Variation in the Threespine Stickleback Gasterosteus aculeatus
title_full_unstemmed Regulatory Architecture of Gene Expression Variation in the Threespine Stickleback Gasterosteus aculeatus
title_short Regulatory Architecture of Gene Expression Variation in the Threespine Stickleback Gasterosteus aculeatus
title_sort regulatory architecture of gene expression variation in the threespine stickleback gasterosteus aculeatus
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217106/
https://www.ncbi.nlm.nih.gov/pubmed/27836907
http://dx.doi.org/10.1534/g3.116.033241
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