Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/129454
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Type: Journal article
Title: Salt-induced expression of intracellular vesicle trafficking genes, CaRab-GTP, and their association with Na⁺ accumulation in leaves of chickpea (Cicer arietinum L.)
Other Titles: Salt-induced expression of intracellular vesicle trafficking genes, CaRab-GTP, and their association with Na(+) accumulation in leaves of chickpea (Cicer arietinum L.)
Author: Sweetman, C.
Khassanova, G.
Miller, T.K.
Booth, N.J.
Kurishbayev, A.
Jatayev, S.
Gupta, N.K.
Langridge, P.
Jenkins, C.L.D.
Soole, K.L.
Day, D.A.
Shavrukov, Y.
Citation: BMC Plant Biology, 2020; 20(Suppl 1):183-1-183-12
Publisher: BMC; Springer Nature
Issue Date: 2020
ISSN: 1471-2229
1471-2229
Statement of
Responsibility: 
Crystal Sweetman, Gulmira Khassanova, Troy K. Miller, Nicholas J. Booth, Akhylbek Kurishbayev, Satyvaldy Jatayev, Narendra K. Gupta, Peter Langridge, Colin L.D. Jenkins, Kathleen L. Soole, David A. Day and Yuri Shavrukov
Abstract: Background: Chickpea is an important legume and is moderately tolerant to salinity stress during the growing season. However, the level and mechanisms for salinity tolerance can vary among accessions and cultivars. A large family of CaRab-GTP genes, previously identified in chickpea, is homologous to intracellular vesicle trafficking superfamily genes that play essential roles in response to salinity stress in plants. Results: To determine which of the gene family members are involved in the chickpea salt response, plants from six selected chickpea accessions (Genesis 836, Hattrick, ICC12726, Rupali, Slasher and Yubileiny) were exposed to salinity stress and expression profiles resolved for the major CaRab-GTP gene clades after 5, 9 and 15 days of salt exposure. Gene clade expression profiles (using degenerate primers targeting all members of each clade) were tested for their relationship to salinity tolerance measures, namely plant biomass and Na+ accumulation. Transcripts representing 11 out of the 13 CaRab clades could be detected by RT-PCR, but only six (CaRabA2, -B, -C, -D, -E and -H) could be quantified using qRT-PCR due to low expression levels or poor amplification efficiency of the degenerate primers for clades containing several gene members. Expression profiles of three gene clades, CaRabB, -D and -E, were very similar across all six chickpea accessions, showing a strongly coordinated network. Salt-induced enhancement of CaRabA2 expression at 15 days showed a very strong positive correlation (R2 = 0.905) with Na+ accumulation in leaves. However, salinity tolerance estimated as relative plant biomass production compared to controls, did not correlate with Na+ accumulation in leaves, nor with expression profiles of any of the investigated CaRab-GTP genes. Conclusion: A coordinated network of CaRab-GTP genes, which are likely involved in intracellular trafficking, are important for the salinity stress response of chickpea plants.
Keywords: Chickpea; gene expression; Rab-GTP genes; salt stress; salinity; vesicle trafficking
Rights: © The Author(s). 2020. 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 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
DOI: 10.1186/s12870-020-02331-5
Grant ID: http://purl.org/au-research/grants/arc/IH140100013
Published version: http://dx.doi.org/10.1186/s12870-020-02331-5
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