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1.
Plant Physiol ; 132(3): 1228-40, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12857805

ABSTRACT

Cytokinins are hormones that play an essential role in plant growth and development. The irreversible degradation of cytokinins, catalyzed by cytokinin oxidase, is an important mechanism by which plants modulate their cytokinin levels. Cytokinin oxidase has been well characterized biochemically, but its regulation at the molecular level is not well understood. We isolated a cytokinin oxidase open reading frame from maize (Zea mays), called Ckx1, and we used it as a probe in northern and in situ hybridization experiments. We found that the gene is expressed in a developmental manner in the kernel, which correlates with cytokinin levels and cytokinin oxidase activity. In situ hybridization with Ckx1 and transgenic expression of a transcriptional fusion of the Ckx1 promoter to the Escherichia coli beta-glucuronidase reporter gene revealed that the gene is expressed in the vascular bundles of kernels, seedling roots, and coleoptiles. We show that Ckx1 gene expression is inducible in various organs by synthetic and natural cytokinins. Ckx1 is also induced by abscisic acid, which may control cytokinin oxidase expression in the kernel under abiotic stress. We hypothesize that under non-stress conditions, cytokinin oxidase in maize plays a role in controlling growth and development via regulation of cytokinin levels transiting in the xylem. In addition, we suggest that under environmental stress conditions, cytokinin oxidase gene induction by abscisic acid results in aberrant degradation of cytokinins therefore impairing normal development.


Subject(s)
Abscisic Acid/pharmacology , Cytokinins/pharmacology , Gene Expression Regulation, Plant/drug effects , Oxidoreductases/metabolism , Zea mays/drug effects , Zea mays/enzymology , Alleles , Cytokinins/metabolism , Dose-Response Relationship, Drug , Gene Expression Profiling , In Situ Hybridization , Oxidoreductases/genetics , Plants, Genetically Modified , RNA, Messenger/genetics , RNA, Messenger/metabolism , RNA, Plant/genetics , RNA, Plant/metabolism , Time Factors , Transcriptional Activation , Zea mays/genetics , Zea mays/growth & development
2.
Plant Cell ; 15(2): 425-38, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12566582

ABSTRACT

Two maize genes with predicted translational similarity to the Arabidopsis FIE (Fertilization-Independent Endosperm) protein, a repressor of endosperm development in the absence of fertilization, were cloned and analyzed. Genomic sequences of fie1 and fie2 show significant homology within coding regions but none within introns or 5' upstream. The fie1 gene is expressed exclusively in the endosperm of developing kernels starting at approximately 6 days after pollination. fie1 is an imprinted gene showing no detectable expression of the paternally derived fie1 allele during kernel development. Conversely, fie2 is expressed in the embryo sac before pollination. After pollination, its expression persists, predominantly in the embryo and at lower levels in the endosperm. The paternal fie2 allele is not expressed early in kernel development, but its transcription is activated at 5 days after pollination. fie2 is likely to be a functional ortholog of the Arabidopsis FIE gene, whereas fie1 has evolved a distinct function. The maize FIE2 and sorghum FIE proteins form a monophyletic group, sharing a closer relationship to each other than to the FIE1 protein, suggesting that maize fie genes originated from two different ancestral genomes.


Subject(s)
Arabidopsis Proteins , Genes, Duplicate/genetics , Plant Proteins/genetics , Repressor Proteins/genetics , Zea mays/genetics , Alleles , Base Sequence , Gene Expression Profiling/methods , Gene Expression Regulation, Developmental , Gene Expression Regulation, Plant , In Situ Hybridization , Molecular Sequence Data , Phylogeny , Plant Proteins/metabolism , Repressor Proteins/metabolism , Seeds/genetics , Seeds/growth & development , Seeds/metabolism , Zea mays/growth & development , Zea mays/metabolism
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