Cytokinin oxidase/dehydrogenase genes in barley and wheat: cloning and heterologous expression
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
15479228
DOI
10.1111/j.1432-1033.2004.04334.x
PII: EJB4334
Knihovny.cz E-zdroje
- MeSH
- 2,6-dichlorindofenol chemie metabolismus MeSH
- Arabidopsis enzymologie genetika růst a vývoj MeSH
- benzochinony chemie metabolismus MeSH
- cytokininy chemie metabolismus MeSH
- exprese genu MeSH
- geneticky modifikované rostliny MeSH
- ječmen (rod) enzymologie genetika MeSH
- klonování DNA MeSH
- koncentrace vodíkových iontů MeSH
- molekulární sekvence - údaje MeSH
- oxidoreduktasy biosyntéza genetika metabolismus MeSH
- pšenice enzymologie genetika MeSH
- rekombinantní proteiny genetika metabolismus MeSH
- rostlinné geny genetika MeSH
- sekvence aminokyselin MeSH
- sekvenční homologie aminokyselin MeSH
- sekvenční seřazení MeSH
- substrátová specifita MeSH
- tabák enzymologie genetika růst a vývoj MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 2,6-dichlorindofenol MeSH
- benzochinony MeSH
- cytokinin oxidase MeSH Prohlížeč
- cytokininy MeSH
- oxidoreduktasy MeSH
- rekombinantní proteiny MeSH
- ubiquinone-O MeSH Prohlížeč
The cloning of two novel genes that encode cytokinin oxidase/dehydrogenase (CKX) in barley is described in this work. Transformation of both genes into Arabidopsis and tobacco showed that at least one of the genes codes for a functional enzyme, as its expression caused a cytokinin-deficient phenotype in the heterologous host plants. Additional cloning of two gene fragments, and an in silico search in the public expressed sequence tag clone databases, revealed the presence of at least 13 more members of the CKX gene family in barley and wheat. The expression of three selected barley genes was analyzed by RT-PCR and found to be organ-specific with peak expression in mature kernels. One barley CKX (HvCKX2) was characterized in detail after heterologous expression in tobacco. Interestingly, this enzyme shows a pH optimum at 4.5 and a preference for cytokinin ribosides as substrates, which may indicate its vacuolar targeting. Different substrate specificities, and the pH profiles of cytokinin-degrading enzymes extracted from different barley tissues, are also presented.
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