Differences in Spatial Expression between 14-3-3 Isoforms in Germinating Barley Embryos
Open Access
- 1 September 1999
- journal article
- Published by Oxford University Press (OUP) in Plant Physiology
- Vol. 121 (1) , 81-88
- https://doi.org/10.1104/pp.121.1.81
Abstract
The family of 14-3-3 proteins is ubiquitous in eukaryotes and has been shown to exert an array of functions. We were interested in the possible role of 14-3-3 proteins in seed germination. Therefore, we studied the expression of 14-3-3 mRNA and protein in barley (Hordeum distichum L.) embryos during germination. With the use of specific cDNA probes and antibodies, we could detect individual expression of three 14-3-3 isoforms, 14-3-3A, 14-3-3B, and 14-3-3C. Each homolog was found to be expressed in barley embryos. Whereas protein levels of all three isoforms were constant during germination, mRNA expression was found to be induced upon imbibition of the grains. The induction of14-3-3A gene expression during germination was different from that of14-3-3B and14-3-3C. In situ immunolocalization analysis showed similar spatial expression for 14-3-3A and 14-3-3B, while 14-3-3C expression was markedly different. Whereas 14-3-3A and 14-3-3B were expressed throughout the embryo, 14-3-3C expression was tissue specific, with the strongest expression observed in the scutellum and the L2 layer of the shoot apical meristem. These results show that 14-3-3 homologs are differently regulated in barley embryos, and provide a first step in acquiring more knowledge about the role of 14-3-3 proteins in the germination process.Keywords
This publication has 26 references indexed in Scilit:
- Deciphering the role of 14-3-3 proteinsExperimental Biology Online, 1998
- Effects of dormancy-breaking chemicals on ABA levels in barley grain embryosSeed Science Research, 1998
- The 14-3-3 protein interacts directly with the C-terminal region of the plant plasma membrane H(+)-ATPase.Plant Cell, 1997
- Topology and target interaction of the fusicoccin‐binding 14‐3‐3 homologs of Commelina communisThe Plant Journal, 1997
- Expression patterns and transcript processing of ftt-1 and ftt-2, two C. elegans 14-3-3 homologuesJournal of Molecular Biology, 1997
- Phosphorylated nitrate reductase from spinach leaves is inhibited by 14-3-3 proteins and activated by fusicoccinCurrent Biology, 1996
- Four Arabidopsis thaliana 14‐3‐3 protein isoforms can complement the lethal yeast bmh1bmh2 double disruptionFEBS Letters, 1996
- Molecular organization and tissue-specific expression of an Arabidopsis 14-3-3 gene.Plant Cell, 1996
- The inhibitor protein of phosphorylated nitrate reductase from spinach (Spinacia oleracea) leaves is a 14‐3‐3 proteinFEBS Letters, 1996
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970