Cargando…

Transcriptome and organellar sequencing highlights the complex origin and diversification of allotetraploid Brassica napus

Brassica napus, an allotetraploid crop, is hypothesized to be a hybrid from unknown varieties of Brassica rapa and Brassica oleracea. Despite the economic importance of B. napus, much is unresolved regarding its phylogenomic relationships, genetic structure, and diversification. Here we conduct a co...

Descripción completa

Detalles Bibliográficos
Autores principales: An, Hong, Qi, Xinshuai, Gaynor, Michelle L., Hao, Yue, Gebken, Sarah C., Mabry, Makenzie E., McAlvay, Alex C., Teakle, Graham R., Conant, Gavin C., Barker, Michael S., Fu, Tingdong, Yi, Bin, Pires, J. Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6599199/
https://www.ncbi.nlm.nih.gov/pubmed/31253789
http://dx.doi.org/10.1038/s41467-019-10757-1
_version_ 1783430912013238272
author An, Hong
Qi, Xinshuai
Gaynor, Michelle L.
Hao, Yue
Gebken, Sarah C.
Mabry, Makenzie E.
McAlvay, Alex C.
Teakle, Graham R.
Conant, Gavin C.
Barker, Michael S.
Fu, Tingdong
Yi, Bin
Pires, J. Chris
author_facet An, Hong
Qi, Xinshuai
Gaynor, Michelle L.
Hao, Yue
Gebken, Sarah C.
Mabry, Makenzie E.
McAlvay, Alex C.
Teakle, Graham R.
Conant, Gavin C.
Barker, Michael S.
Fu, Tingdong
Yi, Bin
Pires, J. Chris
author_sort An, Hong
collection PubMed
description Brassica napus, an allotetraploid crop, is hypothesized to be a hybrid from unknown varieties of Brassica rapa and Brassica oleracea. Despite the economic importance of B. napus, much is unresolved regarding its phylogenomic relationships, genetic structure, and diversification. Here we conduct a comprehensive study among diverse accessions from 183 B. napus (including rapeseed, rutabaga, and Siberian kale), 112 B. rapa, and 62 B. oleracea and its wild relatives. Using RNA-seq of B. napus accessions, we define the genetic diversity and sub-genome variance of six genetic clusters. Nuclear and organellar phylogenies for B. napus and its progenitors reveal varying patterns of inheritance and post-formation introgression. We discern regions with signatures of selective sweeps and detect 8,187 differentially expressed genes with implications for B. napus diversification. This study highlights the complex origin and evolution of B. napus providing insights that can further facilitate B. napus breeding and germplasm preservation.
format Online
Article
Text
id pubmed-6599199
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-65991992019-07-01 Transcriptome and organellar sequencing highlights the complex origin and diversification of allotetraploid Brassica napus An, Hong Qi, Xinshuai Gaynor, Michelle L. Hao, Yue Gebken, Sarah C. Mabry, Makenzie E. McAlvay, Alex C. Teakle, Graham R. Conant, Gavin C. Barker, Michael S. Fu, Tingdong Yi, Bin Pires, J. Chris Nat Commun Article Brassica napus, an allotetraploid crop, is hypothesized to be a hybrid from unknown varieties of Brassica rapa and Brassica oleracea. Despite the economic importance of B. napus, much is unresolved regarding its phylogenomic relationships, genetic structure, and diversification. Here we conduct a comprehensive study among diverse accessions from 183 B. napus (including rapeseed, rutabaga, and Siberian kale), 112 B. rapa, and 62 B. oleracea and its wild relatives. Using RNA-seq of B. napus accessions, we define the genetic diversity and sub-genome variance of six genetic clusters. Nuclear and organellar phylogenies for B. napus and its progenitors reveal varying patterns of inheritance and post-formation introgression. We discern regions with signatures of selective sweeps and detect 8,187 differentially expressed genes with implications for B. napus diversification. This study highlights the complex origin and evolution of B. napus providing insights that can further facilitate B. napus breeding and germplasm preservation. Nature Publishing Group UK 2019-06-28 /pmc/articles/PMC6599199/ /pubmed/31253789 http://dx.doi.org/10.1038/s41467-019-10757-1 Text en © The Author(s) 2019 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
An, Hong
Qi, Xinshuai
Gaynor, Michelle L.
Hao, Yue
Gebken, Sarah C.
Mabry, Makenzie E.
McAlvay, Alex C.
Teakle, Graham R.
Conant, Gavin C.
Barker, Michael S.
Fu, Tingdong
Yi, Bin
Pires, J. Chris
Transcriptome and organellar sequencing highlights the complex origin and diversification of allotetraploid Brassica napus
title Transcriptome and organellar sequencing highlights the complex origin and diversification of allotetraploid Brassica napus
title_full Transcriptome and organellar sequencing highlights the complex origin and diversification of allotetraploid Brassica napus
title_fullStr Transcriptome and organellar sequencing highlights the complex origin and diversification of allotetraploid Brassica napus
title_full_unstemmed Transcriptome and organellar sequencing highlights the complex origin and diversification of allotetraploid Brassica napus
title_short Transcriptome and organellar sequencing highlights the complex origin and diversification of allotetraploid Brassica napus
title_sort transcriptome and organellar sequencing highlights the complex origin and diversification of allotetraploid brassica napus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6599199/
https://www.ncbi.nlm.nih.gov/pubmed/31253789
http://dx.doi.org/10.1038/s41467-019-10757-1
work_keys_str_mv AT anhong transcriptomeandorganellarsequencinghighlightsthecomplexoriginanddiversificationofallotetraploidbrassicanapus
AT qixinshuai transcriptomeandorganellarsequencinghighlightsthecomplexoriginanddiversificationofallotetraploidbrassicanapus
AT gaynormichellel transcriptomeandorganellarsequencinghighlightsthecomplexoriginanddiversificationofallotetraploidbrassicanapus
AT haoyue transcriptomeandorganellarsequencinghighlightsthecomplexoriginanddiversificationofallotetraploidbrassicanapus
AT gebkensarahc transcriptomeandorganellarsequencinghighlightsthecomplexoriginanddiversificationofallotetraploidbrassicanapus
AT mabrymakenziee transcriptomeandorganellarsequencinghighlightsthecomplexoriginanddiversificationofallotetraploidbrassicanapus
AT mcalvayalexc transcriptomeandorganellarsequencinghighlightsthecomplexoriginanddiversificationofallotetraploidbrassicanapus
AT teaklegrahamr transcriptomeandorganellarsequencinghighlightsthecomplexoriginanddiversificationofallotetraploidbrassicanapus
AT conantgavinc transcriptomeandorganellarsequencinghighlightsthecomplexoriginanddiversificationofallotetraploidbrassicanapus
AT barkermichaels transcriptomeandorganellarsequencinghighlightsthecomplexoriginanddiversificationofallotetraploidbrassicanapus
AT futingdong transcriptomeandorganellarsequencinghighlightsthecomplexoriginanddiversificationofallotetraploidbrassicanapus
AT yibin transcriptomeandorganellarsequencinghighlightsthecomplexoriginanddiversificationofallotetraploidbrassicanapus
AT piresjchris transcriptomeandorganellarsequencinghighlightsthecomplexoriginanddiversificationofallotetraploidbrassicanapus