Cytokinin

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Cytokinin metabolisms

M. Kubo and T. Nishiyama

(ku-bo@nibb.ac.jp) (tomoakin@kenroku.kanazawa-u.ac.jp)


Cytokinins (CKs) are N6-substituted adenine derivatives involved in not only cell proliferation and differentiation but also in morphogenesis of tissues and organs in land plants (Kakimoto, 2003). Several key enzymes for CK biosynthesis and metabolisms have been identified (Sakakibara, 2006). CYP735A, a P450 catalyzing next step of IPT reaction were found in only angiosperm lineage. CK oxidases (CKX) catalyze CK degradation by cleavage of its side chain, which play crucial roles in regulating CK levels in plant tissues (Schmülling et al., 2003). We found their potential orthologs in S. moellendorffii and P. patens, but not in the algae. CKX homologs diverged in the each lineage in parallel.


Cytokinin signalling

M. Kubo, T. Aoyama, and T. Nishiyama

(ku-bo@nibb.ac.jp) (tomoakin@kenroku.kanazawa-u.ac.jp)

Cytokinin (CK)signal transduction is mediated by a two-component system with histidine kinases as CK receptors and response regulators (Kakimoto, 2003). We found putative orthologues of the A. thaliana CK receptors in S. moellendorffii and P. patens. The CK receptor land plant orthologues expanded in the angiosperms, S. moellendorffii, and P. patens lineages in parallel. Phosphotransmitters (AHPs), which mediate phosphorylation signals from the CK receptors to response regulators, were found in each land plant lineage and were expanded in each lineage. Response regulators are classified as type-A (ARR-A) or type-B (ARR-B). The ARR-A genes were divided into two groups: ARR22 and other. We found land plant orthologues in each lineage for both groups, indicating these groups separated before the divergence of P. patens from other land plants. The ARR-A homologues expanded in each land plant lineage, which suggests the functional divergence of ARR-A amongst the lineages. All land plants had ARR-B genes, although they diverged more extensively in the angiosperm lineage than in other lineages.


References

Kakimoto, T. (2003). Biosynthesis of cytokinins. Journal Plant Research 116, 233-239.

Kakimoto, T. (2003). Perception and signal transduction of cytokinins. Annu. Rev. Plant Biol. 54, 605-627.

Sakakibara, H. (2006). Cytokinins: Activity, biosynthesis, and translocation. Annual Review of Plant Biology 57, 431-449.

Schmülling, T., Werner, T., Riefler, M., Krupková, E., and Bartrina y Manns, I. (2003). Structure and function of cytokinin oxidase/dehydrogenase genes of maize, rice, Arabidopsis and other species. J. Plant Res. 116, 241-252.


Table of gene numbers

Gene functions Gene Gene used as a query The number of putative orthologs
Arabidopsis thaliana Oryza sativa Selaginalla moellendorffii Physcomitrella patens
Cytokinin metabolisms CYP735A CYP735A1 2 2 0 0
Cytokinin metabolisms CKX CKX7 7 9 3 (5) 6
Cytokinin signalling AHK2, 3, and CRE1/WOL/AHK4 CRE1 3 5 2 (3) 3
Cytokinin signalling AHP1 to 6 AHP2 7 4 2 (4) 3
Cytokinin signalling ARR3 to 9, 15 to 17 ARR5 11 15 2 (4) 7
Cytokinin signalling ARR22 ARR22 2 1 2 (3) 3
Cytokinin signalling ARR1, 2, 10 to 14, 18 to 21, and 23 ARR1 12 9 5 (9) 5


Table of gene models in the assembly

protein id gene name alternate model other name by whom
CKX related genes
98722 CKX1-1
127173 CKX1-2
174721 CKX2-1
106833 CKX2-2
CRE1 related genes
152221 CRE1-1 HK2 heyl
158365 CRE1-2
231095 CRE2-1 HK1 heyl
430773 CRE2-2
AHP2 related genes
267058 HP1-1 HP1 heyl
152299 HP1-2
84165 HP2-1 HP2 heyl
179923 HP2-2
ARR5 related genes
437754 RR7-1 RR7 heyl
444661 RR7-2
445841 RR6-1 RR6 heyl
97144 RR6-2
ARR1 related genes
442188 RR1-1 RR1 heyl
150746 RR1-2
450181 RR2-1 RR2 heyl
173793 RR2-2
418787 RR3-1 RR3 heyl
187683 RR3-2
444702 RR4-1 RR4 heyl
447635 RR4-2
440049 RR5-1 RR5 heyl
115021 RR5-2
ARR22 related genes
451426 HK5-1
449209 HK5-2
451436 HK6-1 PRR6 heyl
451432 HK6-2
genes checked for comparison
451444 SHPK6-1 449750 SHPK6 Jody Banks
451443 SHPK6-2 101918 RR8 heyl
research Groups