TY - JOUR
T1 - Tissue-Specific Proteome and Subcellular Microscopic Analyses Reveal the Effect of High Salt Concentration on Actin Cytoskeleton and Vacuolization in Aleurone Cells during Early Germination of Barley
AU - Dermendjiev, Georgi-Atanasov
AU - Schnurer, Madeleine
AU - Weiszmann, Jakob
AU - Wilfinger, Sarah
AU - Ott, Emanuel
AU - Gebert, Claudia
AU - Weckwerth, Wolfram
AU - Ibl, Verena
N1 - Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/9/6
Y1 - 2021/9/6
N2 - Cereal grain germination provides the basis for crop production and requires a tissue-specific interplay between the embryo and endosperm during heterotrophic germination involving signalling, protein secretion, and nutrient uptake until autotrophic growth is possible. High salt concentrations in soil are one of the most severe constraints limiting the germination of crop plants, affecting the metabolism and redox status within the tissues of germinating seed. However, little is known about the effect of salt on seed storage protein mobilization, the endomembrane system, and protein trafficking within and between these tissues. Here, we used mass spectrometry analyses to investigate the protein dynamics of the embryo and endosperm of barley (Hordeum vulgare, L.) at five different early points during germination (0, 12, 24, 48, and 72 h after imbibition) in germinated grains subjected to salt stress. The expression of proteins in the embryo as well as in the endosperm was temporally regulated. Seed storage proteins (SSPs), peptidases, and starch-digesting enzymes were affected by salt. Additionally, microscopic analyses revealed an altered assembly of actin bundles and morphology of protein storage vacuoles (PSVs) in the aleurone layer. Our results suggest that besides the salt-induced protein expression, intracellular trafficking and actin cytoskeleton assembly are responsible for germination delay under salt stress conditions.
AB - Cereal grain germination provides the basis for crop production and requires a tissue-specific interplay between the embryo and endosperm during heterotrophic germination involving signalling, protein secretion, and nutrient uptake until autotrophic growth is possible. High salt concentrations in soil are one of the most severe constraints limiting the germination of crop plants, affecting the metabolism and redox status within the tissues of germinating seed. However, little is known about the effect of salt on seed storage protein mobilization, the endomembrane system, and protein trafficking within and between these tissues. Here, we used mass spectrometry analyses to investigate the protein dynamics of the embryo and endosperm of barley (Hordeum vulgare, L.) at five different early points during germination (0, 12, 24, 48, and 72 h after imbibition) in germinated grains subjected to salt stress. The expression of proteins in the embryo as well as in the endosperm was temporally regulated. Seed storage proteins (SSPs), peptidases, and starch-digesting enzymes were affected by salt. Additionally, microscopic analyses revealed an altered assembly of actin bundles and morphology of protein storage vacuoles (PSVs) in the aleurone layer. Our results suggest that besides the salt-induced protein expression, intracellular trafficking and actin cytoskeleton assembly are responsible for germination delay under salt stress conditions.
KW - barley
KW - germination
KW - mobilization
KW - vacuolization
KW - proteomics
KW - salt stress
KW - OSMOTIC-STRESS
KW - ACID-INDUCED PROTEIN
KW - CYSTEINE PROTEINASE
KW - GIBBERELLIC-ACID
KW - COMPUTATIONAL PLATFORM
KW - GENE-EXPRESSION
KW - ENDOSPERM DEVELOPMENT
KW - SEED STORAGE PROTEINS
KW - ABSCISIC-ACID
KW - ALPHA-AMYLASE
KW - Barley
KW - Vacuolization
KW - Salt stress
KW - Germination
KW - Mobilization
KW - Proteomics
UR - http://www.scopus.com/inward/record.url?scp=85114267224&partnerID=8YFLogxK
U2 - 10.3390/ijms22179642
DO - 10.3390/ijms22179642
M3 - Article
SN - 1422-0067
VL - 22
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 17
M1 - 9642
ER -