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Sequence and gene expression evolution of paralogous genes in willows

Whole genome duplications (WGD) have had strong impacts on species diversification by triggering evolutionary novelties, however, relatively little is known about the balance between gene loss and forces involved in the retention of duplicated genes originating from a WGD. We analyzed putative Salic...

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Autores principales: Harikrishnan, Srilakshmy L., Pucholt, Pascal, Berlin, Sofia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687058/
https://www.ncbi.nlm.nih.gov/pubmed/26689951
http://dx.doi.org/10.1038/srep18662
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author Harikrishnan, Srilakshmy L.
Pucholt, Pascal
Berlin, Sofia
author_facet Harikrishnan, Srilakshmy L.
Pucholt, Pascal
Berlin, Sofia
author_sort Harikrishnan, Srilakshmy L.
collection PubMed
description Whole genome duplications (WGD) have had strong impacts on species diversification by triggering evolutionary novelties, however, relatively little is known about the balance between gene loss and forces involved in the retention of duplicated genes originating from a WGD. We analyzed putative Salicoid duplicates in willows, originating from the Salicoid WGD, which took place more than 45 Mya. Contigs were constructed by de novo assembly of RNA-seq data derived from leaves and roots from two genotypes. Among the 48,508 contigs, 3,778 pairs were, based on fourfold synonymous third-codon transversion rates and syntenic positions, predicted to be Salicoid duplicates. Both copies were in most cases expressed in both tissues and 74% were significantly differentially expressed. Mean Ka/Ks was 0.23, suggesting that the Salicoid duplicates are evolving by purifying selection. Gene Ontology enrichment analyses showed that functions related to DNA- and nucleic acid binding were over-represented among the non-differentially expressed Salicoid duplicates, while functions related to biosynthesis and metabolism were over-represented among the differentially expressed Salicoid duplicates. We propose that the differentially expressed Salicoid duplicates are regulatory neo- and/or subfunctionalized, while the non-differentially expressed are dose sensitive, hence, functionally conserved. Multiple evolutionary processes, thus drive the retention of Salicoid duplicates in willows.
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spelling pubmed-46870582015-12-31 Sequence and gene expression evolution of paralogous genes in willows Harikrishnan, Srilakshmy L. Pucholt, Pascal Berlin, Sofia Sci Rep Article Whole genome duplications (WGD) have had strong impacts on species diversification by triggering evolutionary novelties, however, relatively little is known about the balance between gene loss and forces involved in the retention of duplicated genes originating from a WGD. We analyzed putative Salicoid duplicates in willows, originating from the Salicoid WGD, which took place more than 45 Mya. Contigs were constructed by de novo assembly of RNA-seq data derived from leaves and roots from two genotypes. Among the 48,508 contigs, 3,778 pairs were, based on fourfold synonymous third-codon transversion rates and syntenic positions, predicted to be Salicoid duplicates. Both copies were in most cases expressed in both tissues and 74% were significantly differentially expressed. Mean Ka/Ks was 0.23, suggesting that the Salicoid duplicates are evolving by purifying selection. Gene Ontology enrichment analyses showed that functions related to DNA- and nucleic acid binding were over-represented among the non-differentially expressed Salicoid duplicates, while functions related to biosynthesis and metabolism were over-represented among the differentially expressed Salicoid duplicates. We propose that the differentially expressed Salicoid duplicates are regulatory neo- and/or subfunctionalized, while the non-differentially expressed are dose sensitive, hence, functionally conserved. Multiple evolutionary processes, thus drive the retention of Salicoid duplicates in willows. Nature Publishing Group 2015-12-22 /pmc/articles/PMC4687058/ /pubmed/26689951 http://dx.doi.org/10.1038/srep18662 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Harikrishnan, Srilakshmy L.
Pucholt, Pascal
Berlin, Sofia
Sequence and gene expression evolution of paralogous genes in willows
title Sequence and gene expression evolution of paralogous genes in willows
title_full Sequence and gene expression evolution of paralogous genes in willows
title_fullStr Sequence and gene expression evolution of paralogous genes in willows
title_full_unstemmed Sequence and gene expression evolution of paralogous genes in willows
title_short Sequence and gene expression evolution of paralogous genes in willows
title_sort sequence and gene expression evolution of paralogous genes in willows
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687058/
https://www.ncbi.nlm.nih.gov/pubmed/26689951
http://dx.doi.org/10.1038/srep18662
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