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Functional Analysis and Marker Development of TaCRT-D Gene in Common Wheat (Triticum aestivum L.)

Calreticulin (CRT), an endoplasmic reticulum (ER)-localized Ca(2+)-binding/buffering protein, is highly conserved and extensively expressed in animal and plant cells. To understand the function of CRTs in wheat (Triticum aestivum L.), particularly their roles in stress tolerance, we cloned the full-...

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Autores principales: Wang, Jiping, Li, Runzhi, Mao, Xinguo, Jing, Ruilian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601976/
https://www.ncbi.nlm.nih.gov/pubmed/28955354
http://dx.doi.org/10.3389/fpls.2017.01557
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author Wang, Jiping
Li, Runzhi
Mao, Xinguo
Jing, Ruilian
author_facet Wang, Jiping
Li, Runzhi
Mao, Xinguo
Jing, Ruilian
author_sort Wang, Jiping
collection PubMed
description Calreticulin (CRT), an endoplasmic reticulum (ER)-localized Ca(2+)-binding/buffering protein, is highly conserved and extensively expressed in animal and plant cells. To understand the function of CRTs in wheat (Triticum aestivum L.), particularly their roles in stress tolerance, we cloned the full-length genomic sequence of the TaCRT-D isoform from D genome of common hexaploid wheat, and characterized its function by transgenic Arabidopsis system. TaCRT-D exhibited different expression patterns in wheat seedling under different abiotic stresses. Transgenic Arabidopsis plants overexpressing ORF of TaCRT-D displayed more tolerance to drought, cold, salt, mannitol, and other abiotic stresses at both seed germination and seedling stages, compared with the wild-type controls. Furthermore, DNA polymorphism analysis and gene mapping were employed to develop the functional markers of this gene for marker-assistant selection in wheat breeding program. One SNP, S440 (T→C) was detected at the TaCRT-D locus by genotyping a wheat recombinant inbred line (RIL) population (114 lines) developed from Opata 85 × W7984. The TaCRT-D was then fine mapped between markers Xgwm645 and Xgwm664 on chromosome 3DL, corresponding to genetic distances of 3.5 and 4.4 cM, respectively, using the RIL population and Chinese Spring nulli-tetrasomic lines. Finally, the genome-specific and allele-specific markers were developed for the TaCRT-D gene. These findings indicate that TaCRT-D function importantly in plant stress responses, providing a gene target for genetic engineering to increase plant stress tolerance and the functional markers of TaCRT-D for marker-assistant selection in wheat breeding.
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spelling pubmed-56019762017-09-27 Functional Analysis and Marker Development of TaCRT-D Gene in Common Wheat (Triticum aestivum L.) Wang, Jiping Li, Runzhi Mao, Xinguo Jing, Ruilian Front Plant Sci Plant Science Calreticulin (CRT), an endoplasmic reticulum (ER)-localized Ca(2+)-binding/buffering protein, is highly conserved and extensively expressed in animal and plant cells. To understand the function of CRTs in wheat (Triticum aestivum L.), particularly their roles in stress tolerance, we cloned the full-length genomic sequence of the TaCRT-D isoform from D genome of common hexaploid wheat, and characterized its function by transgenic Arabidopsis system. TaCRT-D exhibited different expression patterns in wheat seedling under different abiotic stresses. Transgenic Arabidopsis plants overexpressing ORF of TaCRT-D displayed more tolerance to drought, cold, salt, mannitol, and other abiotic stresses at both seed germination and seedling stages, compared with the wild-type controls. Furthermore, DNA polymorphism analysis and gene mapping were employed to develop the functional markers of this gene for marker-assistant selection in wheat breeding program. One SNP, S440 (T→C) was detected at the TaCRT-D locus by genotyping a wheat recombinant inbred line (RIL) population (114 lines) developed from Opata 85 × W7984. The TaCRT-D was then fine mapped between markers Xgwm645 and Xgwm664 on chromosome 3DL, corresponding to genetic distances of 3.5 and 4.4 cM, respectively, using the RIL population and Chinese Spring nulli-tetrasomic lines. Finally, the genome-specific and allele-specific markers were developed for the TaCRT-D gene. These findings indicate that TaCRT-D function importantly in plant stress responses, providing a gene target for genetic engineering to increase plant stress tolerance and the functional markers of TaCRT-D for marker-assistant selection in wheat breeding. Frontiers Media S.A. 2017-09-11 /pmc/articles/PMC5601976/ /pubmed/28955354 http://dx.doi.org/10.3389/fpls.2017.01557 Text en Copyright © 2017 Wang, Li, Mao and Jing. 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) or licensor 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
Wang, Jiping
Li, Runzhi
Mao, Xinguo
Jing, Ruilian
Functional Analysis and Marker Development of TaCRT-D Gene in Common Wheat (Triticum aestivum L.)
title Functional Analysis and Marker Development of TaCRT-D Gene in Common Wheat (Triticum aestivum L.)
title_full Functional Analysis and Marker Development of TaCRT-D Gene in Common Wheat (Triticum aestivum L.)
title_fullStr Functional Analysis and Marker Development of TaCRT-D Gene in Common Wheat (Triticum aestivum L.)
title_full_unstemmed Functional Analysis and Marker Development of TaCRT-D Gene in Common Wheat (Triticum aestivum L.)
title_short Functional Analysis and Marker Development of TaCRT-D Gene in Common Wheat (Triticum aestivum L.)
title_sort functional analysis and marker development of tacrt-d gene in common wheat (triticum aestivum l.)
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601976/
https://www.ncbi.nlm.nih.gov/pubmed/28955354
http://dx.doi.org/10.3389/fpls.2017.01557
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