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NBS-Encoding Genes in Brassica napus Evolved Rapidly After Allopolyploidization and Co-localize With Known Disease Resistance Loci

Genes containing nucleotide-binding sites (NBS) play an important role in pathogen resistance in plants. However, the evolutionary fate of NBS-encoding genes after formation of allotetraploid Brassica napus (A(n)A(n)C(n)C(n), 2n = 38) is still unknown. We performed a genome-wide comparison of putati...

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Autores principales: Fu, Ying, Zhang, Yaofeng, Mason, Annaliese S., Lin, Baogang, Zhang, Dongqing, Yu, Huasheng, Fu, Donghui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363714/
https://www.ncbi.nlm.nih.gov/pubmed/30761170
http://dx.doi.org/10.3389/fpls.2019.00026
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author Fu, Ying
Zhang, Yaofeng
Mason, Annaliese S.
Lin, Baogang
Zhang, Dongqing
Yu, Huasheng
Fu, Donghui
author_facet Fu, Ying
Zhang, Yaofeng
Mason, Annaliese S.
Lin, Baogang
Zhang, Dongqing
Yu, Huasheng
Fu, Donghui
author_sort Fu, Ying
collection PubMed
description Genes containing nucleotide-binding sites (NBS) play an important role in pathogen resistance in plants. However, the evolutionary fate of NBS-encoding genes after formation of allotetraploid Brassica napus (A(n)A(n)C(n)C(n), 2n = 38) is still unknown. We performed a genome-wide comparison of putatively functional NBS-encoding genes in B. napus and its progenitor species Brassica rapa (A(r)A(r), 2n = 20) and Brassica oleracea (C(o)C(o), 2n = 18), identifying 464, 202, and 146 putatively functional NBS-encoding genes respectively, with genes unevenly distributed in several clusters. The A(n)-subgenome of B. napus possessed similar numbers of NBS-encoding genes (191 genes) to the A(r) genome of B. rapa (202 genes) and similar clustering patterns. However, the C(n) genome of B. napus had many more genes (273) than the B. oleracea C(o) genome (146), with different clustering trends. Only 97 NBS-encoding genes (66.4%) in B. oleracea were homologous with NBS-encoding genes in B. napus, while 176 NBS-encoding genes (87.1%) were homologous between B. rapa and B. napus. These results suggest a greater diversification of NBS-encoding genes in the C genome may have occurred after formation of B. napus. Although most NBS-encoding genes in B. napus appeared to derive from the progenitors, the birth and death of several NBS-encoding genes was also putatively mediated by non-homologous recombination. The Ka/Ks values of most homologous pairs between B. napus and the progenitor species were less than 1, suggesting purifying selection during B. napus evolution. The majority of NBS-encoding genes (60% in all species) showed higher expression levels in root tissue (out of root, leaf, stem, seed and flower tissue types). Comparative analysis of NBS-encoding genes with mapped resistance QTL against three major diseases of B. napus (blackleg, clubroot and Sclerotinia stem rot) found 204 NBS-encoding genes in B. napus located within 71 resistance QTL intervals. The majority of NBS-encoding genes were co-located with resistance QTLs against a single disease, while 47 genes were co-located with QTLs against two diseases and 3 genes were co-located with QTLs against all three. Our results revealed significant variation as well as interesting evolutionary trajectories of NBS-encoding genes in the different Brassica subgenomes, while co-localization of NBS-encoding genes and resistance QTL may facilitate resistance breeding in oilseed rape.
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spelling pubmed-63637142019-02-13 NBS-Encoding Genes in Brassica napus Evolved Rapidly After Allopolyploidization and Co-localize With Known Disease Resistance Loci Fu, Ying Zhang, Yaofeng Mason, Annaliese S. Lin, Baogang Zhang, Dongqing Yu, Huasheng Fu, Donghui Front Plant Sci Plant Science Genes containing nucleotide-binding sites (NBS) play an important role in pathogen resistance in plants. However, the evolutionary fate of NBS-encoding genes after formation of allotetraploid Brassica napus (A(n)A(n)C(n)C(n), 2n = 38) is still unknown. We performed a genome-wide comparison of putatively functional NBS-encoding genes in B. napus and its progenitor species Brassica rapa (A(r)A(r), 2n = 20) and Brassica oleracea (C(o)C(o), 2n = 18), identifying 464, 202, and 146 putatively functional NBS-encoding genes respectively, with genes unevenly distributed in several clusters. The A(n)-subgenome of B. napus possessed similar numbers of NBS-encoding genes (191 genes) to the A(r) genome of B. rapa (202 genes) and similar clustering patterns. However, the C(n) genome of B. napus had many more genes (273) than the B. oleracea C(o) genome (146), with different clustering trends. Only 97 NBS-encoding genes (66.4%) in B. oleracea were homologous with NBS-encoding genes in B. napus, while 176 NBS-encoding genes (87.1%) were homologous between B. rapa and B. napus. These results suggest a greater diversification of NBS-encoding genes in the C genome may have occurred after formation of B. napus. Although most NBS-encoding genes in B. napus appeared to derive from the progenitors, the birth and death of several NBS-encoding genes was also putatively mediated by non-homologous recombination. The Ka/Ks values of most homologous pairs between B. napus and the progenitor species were less than 1, suggesting purifying selection during B. napus evolution. The majority of NBS-encoding genes (60% in all species) showed higher expression levels in root tissue (out of root, leaf, stem, seed and flower tissue types). Comparative analysis of NBS-encoding genes with mapped resistance QTL against three major diseases of B. napus (blackleg, clubroot and Sclerotinia stem rot) found 204 NBS-encoding genes in B. napus located within 71 resistance QTL intervals. The majority of NBS-encoding genes were co-located with resistance QTLs against a single disease, while 47 genes were co-located with QTLs against two diseases and 3 genes were co-located with QTLs against all three. Our results revealed significant variation as well as interesting evolutionary trajectories of NBS-encoding genes in the different Brassica subgenomes, while co-localization of NBS-encoding genes and resistance QTL may facilitate resistance breeding in oilseed rape. Frontiers Media S.A. 2019-01-30 /pmc/articles/PMC6363714/ /pubmed/30761170 http://dx.doi.org/10.3389/fpls.2019.00026 Text en Copyright © 2019 Fu, Zhang, Mason, Lin, Zhang, Yu and Fu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Fu, Ying
Zhang, Yaofeng
Mason, Annaliese S.
Lin, Baogang
Zhang, Dongqing
Yu, Huasheng
Fu, Donghui
NBS-Encoding Genes in Brassica napus Evolved Rapidly After Allopolyploidization and Co-localize With Known Disease Resistance Loci
title NBS-Encoding Genes in Brassica napus Evolved Rapidly After Allopolyploidization and Co-localize With Known Disease Resistance Loci
title_full NBS-Encoding Genes in Brassica napus Evolved Rapidly After Allopolyploidization and Co-localize With Known Disease Resistance Loci
title_fullStr NBS-Encoding Genes in Brassica napus Evolved Rapidly After Allopolyploidization and Co-localize With Known Disease Resistance Loci
title_full_unstemmed NBS-Encoding Genes in Brassica napus Evolved Rapidly After Allopolyploidization and Co-localize With Known Disease Resistance Loci
title_short NBS-Encoding Genes in Brassica napus Evolved Rapidly After Allopolyploidization and Co-localize With Known Disease Resistance Loci
title_sort nbs-encoding genes in brassica napus evolved rapidly after allopolyploidization and co-localize with known disease resistance loci
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363714/
https://www.ncbi.nlm.nih.gov/pubmed/30761170
http://dx.doi.org/10.3389/fpls.2019.00026
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