Maize cytokinin dehydrogenase isozymes are localized predominantly to the vacuoles
Language English Country France Media print-electronic
Document type Journal Article
PubMed
27031423
DOI
10.1016/j.plaphy.2016.03.013
PII: S0981-9428(16)30079-1
Knihovny.cz E-resources
- Keywords
- Cytokinin, Cytokinin dehydrogenase, Subcellular localization, Vacuole, Zea mays L.,
- MeSH
- Arabidopsis cytology MeSH
- Endoplasmic Reticulum metabolism MeSH
- Plants, Genetically Modified MeSH
- Intracellular Space metabolism MeSH
- Isoenzymes metabolism MeSH
- Zea mays enzymology MeSH
- Oxidoreductases metabolism MeSH
- Computer Simulation MeSH
- Promoter Regions, Genetic genetics MeSH
- Protein Sorting Signals MeSH
- Protoplasts enzymology MeSH
- Recombinant Fusion Proteins metabolism MeSH
- Plant Cells metabolism MeSH
- Plant Proteins metabolism MeSH
- Suspensions MeSH
- Protein Transport MeSH
- Vacuoles enzymology MeSH
- Green Fluorescent Proteins metabolism MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- cytokinin oxidase MeSH Browser
- Isoenzymes MeSH
- Oxidoreductases MeSH
- Protein Sorting Signals MeSH
- Recombinant Fusion Proteins MeSH
- Plant Proteins MeSH
- Suspensions MeSH
- Green Fluorescent Proteins MeSH
The maize genome encompasses 13 genes encoding for cytokinin dehydrogenase isozymes (CKXs). These enzymes are responsible for irreversible degradation of cytokinin plant hormones and thus, contribute regulating their levels. Here, we focus on the unique aspect of CKXs: their diverse subcellular distribution, important in regulating cytokinin homeostasis. Maize CKXs were tagged with green fluorescent protein (GFP) and transiently expressed in maize protoplasts. Most of the isoforms, namely ZmCKX1, ZmCKX2, ZmCKX4a, ZmCKX5, ZmCKX6, ZmCKX8, ZmCKX9, and ZmCKX12, were associated with endoplasmic reticulum (ER) several hours after transformation. GFP-fused CKXs were observed to accumulate in putative prevacuolar compartments. To gain more information about the spatiotemporal localization of the above isoforms, we prepared stable expression lines of all ZmCKX-GFP fusions in Arabidopsis thaliana Ler suspension culture. All the ER-associated isoforms except ZmCKX1 and ZmCKX9 were found to be targeted primarily to vacuoles, suggesting that ER-localization is a transition point in the intracellular secretory pathway and vacuoles serve as these isoforms' final destination. ZmCKX9 showed an ER-like localization pattern similar to those observed in the transient maize assay. Apoplastic localization of ZmCKX1 was further confirmed and ZmCKX10 showed cytosolic/nuclear localization due to the absence of the signal peptide sequence as previously reported. Additionally, we prepared GFP-fused N-terminal signal deletion mutants of ZmCKX2 and ZmCKX9 and clearly demonstrated that the localization pattern of these mutant forms was cytosolic/nuclear. This study provides the first complex model for spatiotemporal localization of the key enzymes of the cytokinin degradation/catabolism in monocotyledonous plants.
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