» Articles » PMID: 28993661

Metabolic Signatures in Response to Abscisic Acid (ABA) Treatment in Brassica Napus Guard Cells Revealed by Metabolomics

Overview
Journal Sci Rep
Specialty Science
Date 2017 Oct 11
PMID 28993661
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Drought can severely damage crops, resulting in major yield losses. During drought, vascular land plants conserve water via stomatal closure. Each stomate is bordered by a pair of guard cells that shrink in response to drought and the associated hormone abscisic acid (ABA). The activation of complex intracellular signaling networks underlies these responses. Therefore, analysis of guard cell metabolites is fundamental for elucidation of guard cell signaling pathways. Brassica napus is an important oilseed crop for human consumption and biodiesel production. Here, non-targeted metabolomics utilizing gas chromatography mass spectrometry (GC-MS/MS) and liquid chromatography mass spectrometry (LC-MS/MS) were employed for the first time to identify metabolic signatures in response to ABA in B. napus guard cell protoplasts. Metabolome profiling identified 390 distinct metabolites in B. napus guard cells, falling into diverse classes. Of these, 77 metabolites, comprising both primary and secondary metabolites were found to be significantly ABA responsive, including carbohydrates, fatty acids, glucosinolates, and flavonoids. Selected secondary metabolites, sinigrin, quercetin, campesterol, and sitosterol, were confirmed to regulate stomatal closure in Arabidopsis thaliana, B. napus or both species. Information derived from metabolite datasets can provide a blueprint for improvement of water use efficiency and drought tolerance in crops.

Citing Articles

Homoeolog expression divergence contributes to time of day changes in transcriptomic and glucosinolate responses to prolonged water limitation in Brassica napus.

Ricono A, Ludwig E, Casto A, Zorich S, Sumner J, Bird K Plant J. 2025; 121(4):e70011.

PMID: 39993006 PMC: 11849911. DOI: 10.1111/tpj.70011.


Starch metabolism in guard cells: At the intersection of environmental stimuli and stomatal movement.

Dang T, Piro L, Pasini C, Santelia D Plant Physiol. 2024; 196(3):1758-1777.

PMID: 39115378 PMC: 11531838. DOI: 10.1093/plphys/kiae414.


Plant Secondary Metabolites: The Weapons for Biotic Stress Management.

Al-Khayri J, Rashmi R, Toppo V, Chole P, Banadka A, Sudheer W Metabolites. 2023; 13(6).

PMID: 37367873 PMC: 10302943. DOI: 10.3390/metabo13060716.


Genome-wide investigation and expression profiling of gene family in rapeseed under salinity and ABA stress.

Yang S, Chen J, Ding Y, Huang Q, Chen G, Ulhassan Z Front Plant Sci. 2023; 14:1197781.

PMID: 37324688 PMC: 10264818. DOI: 10.3389/fpls.2023.1197781.


Non-canonical and developmental roles of the TCA cycle in plants.

Zhang T, Peng J, Klair A, Dickinson A Curr Opin Plant Biol. 2023; 74:102382.

PMID: 37210789 PMC: 10524895. DOI: 10.1016/j.pbi.2023.102382.


References
1.
de Bekker C, Smith P, Patterson A, Hughes D . Metabolomics reveals the heterogeneous secretome of two entomopathogenic fungi to ex vivo cultured insect tissues. PLoS One. 2013; 8(8):e70609. PMC: 3734240. DOI: 10.1371/journal.pone.0070609. View

2.
Xia J, Sinelnikov I, Han B, Wishart D . MetaboAnalyst 3.0--making metabolomics more meaningful. Nucleic Acids Res. 2015; 43(W1):W251-7. PMC: 4489235. DOI: 10.1093/nar/gkv380. View

3.
Lee S, Luan S . ABA signal transduction at the crossroad of biotic and abiotic stress responses. Plant Cell Environ. 2011; 35(1):53-60. DOI: 10.1111/j.1365-3040.2011.02426.x. View

4.
Reichelt M, Brown P, Schneider B, Oldham N, Stauber E, Tokuhisa J . Benzoic acid glucosinolate esters and other glucosinolates from Arabidopsis thaliana. Phytochemistry. 2002; 59(6):663-71. DOI: 10.1016/s0031-9422(02)00014-6. View

5.
Witkowski E, Lamont B . Leaf specific mass confounds leaf density and thickness. Oecologia. 2017; 88(4):486-493. DOI: 10.1007/BF00317710. View