Cargando…
Evolutionary shifts in gene expression decoupled from gene duplication across functionally distinct spider silk glands
Spider silk synthesis is an emerging model for the evolution of tissue-specific gene expression and the role of gene duplication in functional novelty, but its potential has not been fully realized. Accordingly, we quantified transcript (mRNA) abundance in seven silk gland types and three non-silk g...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566633/ https://www.ncbi.nlm.nih.gov/pubmed/28827773 http://dx.doi.org/10.1038/s41598-017-07388-1 |
_version_ | 1783258584833851392 |
---|---|
author | Clarke, Thomas H. Garb, Jessica E. Haney, Robert A. Chaw, R. Crystal Hayashi, Cheryl Y. Ayoub, Nadia A. |
author_facet | Clarke, Thomas H. Garb, Jessica E. Haney, Robert A. Chaw, R. Crystal Hayashi, Cheryl Y. Ayoub, Nadia A. |
author_sort | Clarke, Thomas H. |
collection | PubMed |
description | Spider silk synthesis is an emerging model for the evolution of tissue-specific gene expression and the role of gene duplication in functional novelty, but its potential has not been fully realized. Accordingly, we quantified transcript (mRNA) abundance in seven silk gland types and three non-silk gland tissues for three cobweb-weaving spider species. Evolutionary analyses based on expression levels of thousands of homologous transcripts and phylogenetic reconstruction of 605 gene families demonstrated conservation of expression for each gland type among species. Despite serial homology of all silk glands, the expression profiles of the glue-forming aggregate glands were divergent from fiber-forming glands. Also surprising was our finding that shifts in gene expression among silk gland types were not necessarily coupled with gene duplication, even though silk-specific genes belong to multi-paralog gene families. Our results challenge widely accepted models of tissue specialization and significantly advance efforts to replicate silk-based high-performance biomaterials. |
format | Online Article Text |
id | pubmed-5566633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55666332017-09-01 Evolutionary shifts in gene expression decoupled from gene duplication across functionally distinct spider silk glands Clarke, Thomas H. Garb, Jessica E. Haney, Robert A. Chaw, R. Crystal Hayashi, Cheryl Y. Ayoub, Nadia A. Sci Rep Article Spider silk synthesis is an emerging model for the evolution of tissue-specific gene expression and the role of gene duplication in functional novelty, but its potential has not been fully realized. Accordingly, we quantified transcript (mRNA) abundance in seven silk gland types and three non-silk gland tissues for three cobweb-weaving spider species. Evolutionary analyses based on expression levels of thousands of homologous transcripts and phylogenetic reconstruction of 605 gene families demonstrated conservation of expression for each gland type among species. Despite serial homology of all silk glands, the expression profiles of the glue-forming aggregate glands were divergent from fiber-forming glands. Also surprising was our finding that shifts in gene expression among silk gland types were not necessarily coupled with gene duplication, even though silk-specific genes belong to multi-paralog gene families. Our results challenge widely accepted models of tissue specialization and significantly advance efforts to replicate silk-based high-performance biomaterials. Nature Publishing Group UK 2017-08-21 /pmc/articles/PMC5566633/ /pubmed/28827773 http://dx.doi.org/10.1038/s41598-017-07388-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Clarke, Thomas H. Garb, Jessica E. Haney, Robert A. Chaw, R. Crystal Hayashi, Cheryl Y. Ayoub, Nadia A. Evolutionary shifts in gene expression decoupled from gene duplication across functionally distinct spider silk glands |
title | Evolutionary shifts in gene expression decoupled from gene duplication across functionally distinct spider silk glands |
title_full | Evolutionary shifts in gene expression decoupled from gene duplication across functionally distinct spider silk glands |
title_fullStr | Evolutionary shifts in gene expression decoupled from gene duplication across functionally distinct spider silk glands |
title_full_unstemmed | Evolutionary shifts in gene expression decoupled from gene duplication across functionally distinct spider silk glands |
title_short | Evolutionary shifts in gene expression decoupled from gene duplication across functionally distinct spider silk glands |
title_sort | evolutionary shifts in gene expression decoupled from gene duplication across functionally distinct spider silk glands |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566633/ https://www.ncbi.nlm.nih.gov/pubmed/28827773 http://dx.doi.org/10.1038/s41598-017-07388-1 |
work_keys_str_mv | AT clarkethomash evolutionaryshiftsingeneexpressiondecoupledfromgeneduplicationacrossfunctionallydistinctspidersilkglands AT garbjessicae evolutionaryshiftsingeneexpressiondecoupledfromgeneduplicationacrossfunctionallydistinctspidersilkglands AT haneyroberta evolutionaryshiftsingeneexpressiondecoupledfromgeneduplicationacrossfunctionallydistinctspidersilkglands AT chawrcrystal evolutionaryshiftsingeneexpressiondecoupledfromgeneduplicationacrossfunctionallydistinctspidersilkglands AT hayashicheryly evolutionaryshiftsingeneexpressiondecoupledfromgeneduplicationacrossfunctionallydistinctspidersilkglands AT ayoubnadiaa evolutionaryshiftsingeneexpressiondecoupledfromgeneduplicationacrossfunctionallydistinctspidersilkglands |