Proteomic Analysis of Seedling Roots of Two Maize Inbred Lines That Differ Significantly in the Salt Stress Response
0301 basic medicine
genotype
Arabidopsis
maize
Plant Roots
630
cysteine proteinase
adenosylhomocysteinase
histone H4
plant structures
plant protein
pathogenesis related protein 10
adenine nucleotide translocase
vegetable protein
sucrose synthase
comparative study
Plant Proteins
2. Zero hunger
potassium
Q
seed maturation protein PM41
R
plasma membrane intrinsic protein 2
plasma membrane intrinsic protein 1
sodium ion
gene control
Salt Tolerance
exhydrolase II isoform 1
cross tolerance
unclassified drug
genotype F35
sodium chloride
Medicine
down regulation
Research Article
570
Genotype
lichenase 2 precursor
phenotype
Science
water
formate dehydrogenase
ribosomal protein S8
Zea mays
Article
osmotic potential
03 medical and health sciences
alpha 1,4 glucan protein synthase
Species Specificity
Stress, Physiological
controlled study
heat shock protein 90
genotype F63
protein expression
maize insect resistance 1
nonhuman
plant root
peroxidase 42 precursor
protein GST 4
barley
aquaporin
fructose bisphosphate aldolase
xyloglucan endotransglycosylase
protein 14 3 3
plasma membrane intrinsic protein[2-4]
inbred strain
fructokinase 2
DOI:
10.1371/journal.pone.0116697
Publication Date:
2015-02-06T21:44:45Z
AUTHORS (14)
ABSTRACT
Salinity is a major abiotic stress that limits plant productivity and quality throughout the world. Roots are the sites of salt uptake. To better understand salt stress responses in maize, we performed a comparative proteomic analysis of seedling roots from the salt-tolerant genotype F63 and the salt-sensitive genotype F35 under 160 mM NaCl treatment for 2 days. Under salinity conditions, the shoot fresh weight and relative water content were significantly higher in F63 than in F35, while the osmotic potential was significantly lower and the reduction of the K+/Na+ ratio was significantly less pronounced in F63 than in F35. Using an iTRAQ approach, twenty-eight proteins showed more than 2.0- fold changes in abundance and were regarded as salt-responsive proteins. Among them, twenty-two were specifically regulated in F63 but remained constant in F35. These proteins were mainly involved in signal processing, water conservation, protein synthesis and biotic cross-tolerance, and could be the major contributors to the tolerant genotype of F63. Functional analysis of a salt-responsive protein was performed in yeast as a case study to confirm the salt-related functions of detected proteins. Taken together, the results of this study may be helpful for further elucidating salt tolerance mechanisms in maize.
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CITATIONS (40)
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