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Dominance and Sexual Dimorphism Pervade the Salix purpurea L. Transcriptome

The heritability of gene expression is critical in understanding heterosis and is dependent on allele-specific regulation by local and remote factors in the genome. We used RNA-Seq to test whether variation in gene expression among F(1) and F(2) intraspecific Salix purpurea progeny is attributable t...

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Autores principales: Carlson, Craig H., Choi, Yongwook, Chan, Agnes P., Serapiglia, Michelle J., Town, Christopher D., Smart, Lawrence B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622329/
https://www.ncbi.nlm.nih.gov/pubmed/28957462
http://dx.doi.org/10.1093/gbe/evx174
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author Carlson, Craig H.
Choi, Yongwook
Chan, Agnes P.
Serapiglia, Michelle J.
Town, Christopher D.
Smart, Lawrence B.
author_facet Carlson, Craig H.
Choi, Yongwook
Chan, Agnes P.
Serapiglia, Michelle J.
Town, Christopher D.
Smart, Lawrence B.
author_sort Carlson, Craig H.
collection PubMed
description The heritability of gene expression is critical in understanding heterosis and is dependent on allele-specific regulation by local and remote factors in the genome. We used RNA-Seq to test whether variation in gene expression among F(1) and F(2) intraspecific Salix purpurea progeny is attributable to cis- and trans-regulatory divergence. We assessed the mode of inheritance based on gene expression levels and allele-specific expression for F(1) and F(2) intraspecific progeny in two distinct tissue types: shoot tip and stem internode. In addition, we explored sexually dimorphic patterns of inheritance and regulatory divergence among F(1) progeny individuals. We show that in S. purpurea intraspecific crosses, gene expression inheritance largely exhibits a maternal dominant pattern, regardless of tissue type or pedigree. A significantly greater number of cis- and trans-regulated genes coincided with upregulation of the maternal parent allele in the progeny, irrespective of the magnitude, whereas the paternal allele was higher expressed for genes showing cis × trans or compensatory regulation. Importantly, consistent with previous genetic mapping results for sex in shrub willow, we have delimited sex-biased gene expression to a 2 Mb pericentromeric region on S. purpurea chr15 and further refined the sex determination region. Altogether, our results offer insight into the inheritance of gene expression in S. purpurea as well as evidence of sexually dimorphic expression which may have contributed to the evolution of dioecy in Salix.
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spelling pubmed-56223292017-10-04 Dominance and Sexual Dimorphism Pervade the Salix purpurea L. Transcriptome Carlson, Craig H. Choi, Yongwook Chan, Agnes P. Serapiglia, Michelle J. Town, Christopher D. Smart, Lawrence B. Genome Biol Evol Research Article The heritability of gene expression is critical in understanding heterosis and is dependent on allele-specific regulation by local and remote factors in the genome. We used RNA-Seq to test whether variation in gene expression among F(1) and F(2) intraspecific Salix purpurea progeny is attributable to cis- and trans-regulatory divergence. We assessed the mode of inheritance based on gene expression levels and allele-specific expression for F(1) and F(2) intraspecific progeny in two distinct tissue types: shoot tip and stem internode. In addition, we explored sexually dimorphic patterns of inheritance and regulatory divergence among F(1) progeny individuals. We show that in S. purpurea intraspecific crosses, gene expression inheritance largely exhibits a maternal dominant pattern, regardless of tissue type or pedigree. A significantly greater number of cis- and trans-regulated genes coincided with upregulation of the maternal parent allele in the progeny, irrespective of the magnitude, whereas the paternal allele was higher expressed for genes showing cis × trans or compensatory regulation. Importantly, consistent with previous genetic mapping results for sex in shrub willow, we have delimited sex-biased gene expression to a 2 Mb pericentromeric region on S. purpurea chr15 and further refined the sex determination region. Altogether, our results offer insight into the inheritance of gene expression in S. purpurea as well as evidence of sexually dimorphic expression which may have contributed to the evolution of dioecy in Salix. Oxford University Press 2017-09-01 /pmc/articles/PMC5622329/ /pubmed/28957462 http://dx.doi.org/10.1093/gbe/evx174 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 Research Article
Carlson, Craig H.
Choi, Yongwook
Chan, Agnes P.
Serapiglia, Michelle J.
Town, Christopher D.
Smart, Lawrence B.
Dominance and Sexual Dimorphism Pervade the Salix purpurea L. Transcriptome
title Dominance and Sexual Dimorphism Pervade the Salix purpurea L. Transcriptome
title_full Dominance and Sexual Dimorphism Pervade the Salix purpurea L. Transcriptome
title_fullStr Dominance and Sexual Dimorphism Pervade the Salix purpurea L. Transcriptome
title_full_unstemmed Dominance and Sexual Dimorphism Pervade the Salix purpurea L. Transcriptome
title_short Dominance and Sexual Dimorphism Pervade the Salix purpurea L. Transcriptome
title_sort dominance and sexual dimorphism pervade the salix purpurea l. transcriptome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622329/
https://www.ncbi.nlm.nih.gov/pubmed/28957462
http://dx.doi.org/10.1093/gbe/evx174
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