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HvNCX, a prime candidate gene for the novel qualitative locus qS7.1 associated with salinity tolerance in barley

KEY MESSAGE: A major QTL (qS7.1) for salinity damage score and Na+ exclusion was identified on chromosome 7H from a barley population derived from a cross between a cultivated variety and a wild accession. qS7.1 was fine-mapped to a 2.46 Mb physical interval and HvNCX encoding a sodium/calcium excha...

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Autores principales: Zhu, Juan, Zhou, Hui, Fan, Yun, Guo, Yu, Zhang, Mengna, Shabala, Sergey, Zhao, Chenchen, Lv, Chao, Guo, Baojian, Wang, Feifei, Zhou, Meixue, Xu, Rugen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9852152/
https://www.ncbi.nlm.nih.gov/pubmed/36656369
http://dx.doi.org/10.1007/s00122-023-04267-4
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author Zhu, Juan
Zhou, Hui
Fan, Yun
Guo, Yu
Zhang, Mengna
Shabala, Sergey
Zhao, Chenchen
Lv, Chao
Guo, Baojian
Wang, Feifei
Zhou, Meixue
Xu, Rugen
author_facet Zhu, Juan
Zhou, Hui
Fan, Yun
Guo, Yu
Zhang, Mengna
Shabala, Sergey
Zhao, Chenchen
Lv, Chao
Guo, Baojian
Wang, Feifei
Zhou, Meixue
Xu, Rugen
author_sort Zhu, Juan
collection PubMed
description KEY MESSAGE: A major QTL (qS7.1) for salinity damage score and Na+ exclusion was identified on chromosome 7H from a barley population derived from a cross between a cultivated variety and a wild accession. qS7.1 was fine-mapped to a 2.46 Mb physical interval and HvNCX encoding a sodium/calcium exchanger is most likely the candidate gene. ABSTRACT: Soil salinity is one of the major abiotic stresses affecting crop yield. Developing salinity-tolerant varieties is critical for minimizing economic penalties caused by salinity and providing solutions for global food security. Many genes/QTL for salt tolerance have been reported in barley, but only a few of them have been cloned. In this study, a total of 163 doubled haploid lines from a cross between a cultivated barley variety Franklin and a wild barley accession TAM407227 were used to map QTL for salinity tolerance. Four significant QTL were identified for salinity damage scores. One (qS2.1) was located on 2H, determining 7.5% of the phenotypic variation. Two (qS5.1 and qS5.2) were located on 5H, determining 5.3–11.7% of the phenotypic variation. The most significant QTL was found on 7H, explaining 27.8% of the phenotypic variation. Two QTL for Na(+) content in leaves under salinity stress were detected on chromosomes 1H (qNa1.1) and 7H(qNa7.1). qS7.1 was fine-mapped to a 2.46 Mb physical interval using F(4) recombinant inbred lines. This region contains 23 high-confidence genes, with HvNCX which encodes a sodium/calcium exchanger being most likely the candidate gene. HvNCX was highly induced by salinity stress and showed a greater expression level in the sensitive parent. Multiple nucleotide substitutions and deletions/insertions in the promoter sequence of HvNCX were found between the two parents. cDNA sequencing of the HvNCX revealed that the difference between the two parents is conferred by a single Ala77/Pro77 amino acid substitution, which is located on the transmembrane domain. These findings open new prospects for improving salinity tolerance in barley by targeting a previously unexplored trait. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00122-023-04267-4.
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spelling pubmed-98521522023-01-21 HvNCX, a prime candidate gene for the novel qualitative locus qS7.1 associated with salinity tolerance in barley Zhu, Juan Zhou, Hui Fan, Yun Guo, Yu Zhang, Mengna Shabala, Sergey Zhao, Chenchen Lv, Chao Guo, Baojian Wang, Feifei Zhou, Meixue Xu, Rugen Theor Appl Genet Original Article KEY MESSAGE: A major QTL (qS7.1) for salinity damage score and Na+ exclusion was identified on chromosome 7H from a barley population derived from a cross between a cultivated variety and a wild accession. qS7.1 was fine-mapped to a 2.46 Mb physical interval and HvNCX encoding a sodium/calcium exchanger is most likely the candidate gene. ABSTRACT: Soil salinity is one of the major abiotic stresses affecting crop yield. Developing salinity-tolerant varieties is critical for minimizing economic penalties caused by salinity and providing solutions for global food security. Many genes/QTL for salt tolerance have been reported in barley, but only a few of them have been cloned. In this study, a total of 163 doubled haploid lines from a cross between a cultivated barley variety Franklin and a wild barley accession TAM407227 were used to map QTL for salinity tolerance. Four significant QTL were identified for salinity damage scores. One (qS2.1) was located on 2H, determining 7.5% of the phenotypic variation. Two (qS5.1 and qS5.2) were located on 5H, determining 5.3–11.7% of the phenotypic variation. The most significant QTL was found on 7H, explaining 27.8% of the phenotypic variation. Two QTL for Na(+) content in leaves under salinity stress were detected on chromosomes 1H (qNa1.1) and 7H(qNa7.1). qS7.1 was fine-mapped to a 2.46 Mb physical interval using F(4) recombinant inbred lines. This region contains 23 high-confidence genes, with HvNCX which encodes a sodium/calcium exchanger being most likely the candidate gene. HvNCX was highly induced by salinity stress and showed a greater expression level in the sensitive parent. Multiple nucleotide substitutions and deletions/insertions in the promoter sequence of HvNCX were found between the two parents. cDNA sequencing of the HvNCX revealed that the difference between the two parents is conferred by a single Ala77/Pro77 amino acid substitution, which is located on the transmembrane domain. These findings open new prospects for improving salinity tolerance in barley by targeting a previously unexplored trait. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00122-023-04267-4. Springer Berlin Heidelberg 2023-01-19 2023 /pmc/articles/PMC9852152/ /pubmed/36656369 http://dx.doi.org/10.1007/s00122-023-04267-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Zhu, Juan
Zhou, Hui
Fan, Yun
Guo, Yu
Zhang, Mengna
Shabala, Sergey
Zhao, Chenchen
Lv, Chao
Guo, Baojian
Wang, Feifei
Zhou, Meixue
Xu, Rugen
HvNCX, a prime candidate gene for the novel qualitative locus qS7.1 associated with salinity tolerance in barley
title HvNCX, a prime candidate gene for the novel qualitative locus qS7.1 associated with salinity tolerance in barley
title_full HvNCX, a prime candidate gene for the novel qualitative locus qS7.1 associated with salinity tolerance in barley
title_fullStr HvNCX, a prime candidate gene for the novel qualitative locus qS7.1 associated with salinity tolerance in barley
title_full_unstemmed HvNCX, a prime candidate gene for the novel qualitative locus qS7.1 associated with salinity tolerance in barley
title_short HvNCX, a prime candidate gene for the novel qualitative locus qS7.1 associated with salinity tolerance in barley
title_sort hvncx, a prime candidate gene for the novel qualitative locus qs7.1 associated with salinity tolerance in barley
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9852152/
https://www.ncbi.nlm.nih.gov/pubmed/36656369
http://dx.doi.org/10.1007/s00122-023-04267-4
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