Spike developmental stages and ABA role in spikelet primordia abortion contribute to the final yield in barley (Hordeum vulgare L.).

ABA Barley Primordia abortion Salinity Spike development Spikelet/floret abortion

Journal

Botanical studies
ISSN: 1817-406X
Titre abrégé: Bot Stud
Pays: England
ID NLM: 101321928

Informations de publication

Date de publication:
10 Jul 2019
Historique:
received: 21 05 2019
accepted: 03 07 2019
entrez: 12 7 2019
pubmed: 12 7 2019
medline: 12 7 2019
Statut: epublish

Résumé

Salinity is a significant environmental stress factor limiting crops productivity. Barley (Hordeum vulgare L.) has a natural tolerance to salinity stress, making it an interesting study object in stress biology research. In the present study, for the first time the effect of salinity stress on barley inflorescence developmental stages was investigated. Five spring barley genotypes irrigated with saline water (12.5 ds/m NaCl) were compared to controls treated with normal tap water. We measured abscisic acid (ABA) concentrations in the apical, central and basal sections of the immature inflorescence at green anther (GA) stage. The role of ABA in spikelet primordia development, atrophy and abortion and final yield was evaluated. A time course experiment starting from double ridge until green anther (GA) stages revealed that salinity reduced the length of spike developmental stages in all genotypes causing shortened of the plant life cycle. The shortened plant life cycle negatively affected plant height and number of tillers/plant. Salinity also affected spikelet primordia development. In both control and salinity treated plants apical spikelet abortion started in late awn primordium (AP) stage. However, under salinity treatment, significantly more spikelets were aborted, thus directly affecting plant yield potential. ABA, which plays a role in the spikelet/floret abortion process, was markedly elevated in the base and apex of salt treated spikes correlating with an increased spikelet abortion in these regions. Overall, salinity treatment reduced all plant and yield-related parameters investigated and turned some of the correlations among them from positive to negative or vice versa. Investigations of ABA role in floral development and phase duration of barley spike showed that, ABA regulates the spikelet/floret abortion process affecting the yield potential under salinity and control conditions.

Sections du résumé

BACKGROUND BACKGROUND
Salinity is a significant environmental stress factor limiting crops productivity. Barley (Hordeum vulgare L.) has a natural tolerance to salinity stress, making it an interesting study object in stress biology research. In the present study, for the first time the effect of salinity stress on barley inflorescence developmental stages was investigated. Five spring barley genotypes irrigated with saline water (12.5 ds/m NaCl) were compared to controls treated with normal tap water. We measured abscisic acid (ABA) concentrations in the apical, central and basal sections of the immature inflorescence at green anther (GA) stage. The role of ABA in spikelet primordia development, atrophy and abortion and final yield was evaluated.
RESULTS RESULTS
A time course experiment starting from double ridge until green anther (GA) stages revealed that salinity reduced the length of spike developmental stages in all genotypes causing shortened of the plant life cycle. The shortened plant life cycle negatively affected plant height and number of tillers/plant. Salinity also affected spikelet primordia development. In both control and salinity treated plants apical spikelet abortion started in late awn primordium (AP) stage. However, under salinity treatment, significantly more spikelets were aborted, thus directly affecting plant yield potential. ABA, which plays a role in the spikelet/floret abortion process, was markedly elevated in the base and apex of salt treated spikes correlating with an increased spikelet abortion in these regions.
CONCLUSIONS CONCLUSIONS
Overall, salinity treatment reduced all plant and yield-related parameters investigated and turned some of the correlations among them from positive to negative or vice versa. Investigations of ABA role in floral development and phase duration of barley spike showed that, ABA regulates the spikelet/floret abortion process affecting the yield potential under salinity and control conditions.

Identifiants

pubmed: 31292768
doi: 10.1186/s40529-019-0261-2
pii: 10.1186/s40529-019-0261-2
pmc: PMC6620232
doi:

Types de publication

Journal Article

Langues

eng

Pagination

13

Références

Nat Genet. 2017 Jan;49(1):157-161
pubmed: 27841879
Pak J Biol Sci. 2009 Apr 15;12(8):624-30
pubmed: 19634487
Plant Physiol. 2013 Nov;163(3):1433-45
pubmed: 24085801
Front Genet. 2014 Aug 13;5:218
pubmed: 25165468
Genet Mol Res. 2012 Mar 19;11(1):679-92
pubmed: 22535404
Plant Biotechnol (Tokyo). 2018 Sep 25;35(3):193-206
pubmed: 31819724
Methods Mol Biol. 2011;773:99-111
pubmed: 21898252
Plant Physiol Biochem. 2013 Feb;63:49-60
pubmed: 23232247
Plant Physiol. 1996 Sep;112(1):379-384
pubmed: 12226396
Plant Physiol Biochem. 2017 Oct;119:294-311
pubmed: 28938176
Plant Cell Environ. 2010 Apr;33(4):510-25
pubmed: 19843256
J Exp Bot. 2008;59(15):4119-31
pubmed: 19036841
Plant Cell Physiol. 2009 Jul;50(7):1201-14
pubmed: 19369275
Planta. 2000 Jan;210(2):222-31
pubmed: 10664128
Plant Mol Biol. 2013 Nov;83(4-5):475-88
pubmed: 23846670
Plant Physiol. 1998 Dec;118(4):1507-15
pubmed: 9847127
Plant Cell Environ. 2012 Jan;35(1):53-60
pubmed: 21923759
J Neurosci. 2012 Mar 7;32(10):3306-20
pubmed: 22399753
Plant Physiol. 2013 Aug;162(4):2028-41
pubmed: 23800991
Ann Bot. 2007 Nov;100(5):999-1008
pubmed: 17761690
EMBO Rep. 2001 Oct;2(10):877-9
pubmed: 11600447
Plant Cell Rep. 2019 Aug;38(8):1013-1016
pubmed: 31139893
Funct Plant Biol. 2014 Apr;41(4):424-436
pubmed: 32481002
PLoS One. 2016 Jan 29;11(1):e0147625
pubmed: 26824246
Methods Mol Biol. 2009;495:53-60
pubmed: 19085147
New Phytol. 2005 Sep;167(3):645-63
pubmed: 16101905
Science. 1997 Dec 19;278(5346):2126-30
pubmed: 9405349
Mol Plant. 2011 Jul;4(4):616-25
pubmed: 21357646
J Exp Bot. 2008;59(11):3039-50
pubmed: 18573798

Auteurs

Faiza Boussora (F)

Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Corrensstraße 3, 06466, Gatersleben, Germany.
Institute of Arid Lands of Medenine, Route du Djorf Km 22.5, Médénine, Tunisia.
Faculty of Sciences of Bizerte (FSB), 7021 Zarzouna, Bizerte, Tunisia.

Mohamed Allam (M)

Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Corrensstraße 3, 06466, Gatersleben, Germany.
Institute of Agriculture, Lithuanian Research Centre for Agriculture and Forestry, Akademija, Lithuania.

Ferdaous Guasmi (F)

Institute of Arid Lands of Medenine, Route du Djorf Km 22.5, Médénine, Tunisia.

Ali Ferchichi (A)

Institut National Agronomique de Tunis, 43 Avenue Charles Nicolle, 1082, Tunis, Tunisia.

Twan Rutten (T)

Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Corrensstraße 3, 06466, Gatersleben, Germany.

Mats Hansson (M)

Department of Biology, Lund University, Sölvegatan 35, 22362, Lund, Sweden.

Helmy M Youssef (HM)

Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Corrensstraße 3, 06466, Gatersleben, Germany. Youssef@ipk-gatersleben.de.
Faculty of Agriculture, Cairo University, Giza, 12613, Egypt. Youssef@ipk-gatersleben.de.
Department of Biology, Lund University, Sölvegatan 35, 22362, Lund, Sweden. Youssef@ipk-gatersleben.de.

Andreas Börner (A)

Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Corrensstraße 3, 06466, Gatersleben, Germany. boerner@ipk-gatersleben.de.

Classifications MeSH