2010
DOI: 10.1007/s00344-010-9155-y
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Comparative Expression and Phylogenetic Analysis of Maize Cytokinin Dehydrogenase/Oxidase (CKX) Gene Family

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Cited by 52 publications
(54 citation statements)
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“…The spatial and temporal distributions of bioactive cytokinin level are also strictly controlled for plant development events. There exist 11 genes encoding for CKX in the rice genome, with two sets of segmental duplication genes (OsCKX4/ OsCKX9 and OsCKX3/OsCKX8) and a pair of tandem duplication genes (OsCKX6/OsCKX7; Ashikari et al, 2005;Gu et al, 2010). Although some characterizations of OsCKX genes have been reported recently Tsai et al, 2012), only OsCKX2 has been characterized in detail to date.…”
Section: Discussionmentioning
confidence: 99%
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“…The spatial and temporal distributions of bioactive cytokinin level are also strictly controlled for plant development events. There exist 11 genes encoding for CKX in the rice genome, with two sets of segmental duplication genes (OsCKX4/ OsCKX9 and OsCKX3/OsCKX8) and a pair of tandem duplication genes (OsCKX6/OsCKX7; Ashikari et al, 2005;Gu et al, 2010). Although some characterizations of OsCKX genes have been reported recently Tsai et al, 2012), only OsCKX2 has been characterized in detail to date.…”
Section: Discussionmentioning
confidence: 99%
“…A BLAST search indicated that OsCKX4 contains a FAD-binding domain located at its N terminus and a cytokinin-binding site located at its C terminus. Phylogenetic analysis shows that OsCKX4 is more closely related to Arabidopsis CKX proteins, indicating that separation of the present CKX genes occurred before the separation of monocot and dicot plants Gu et al, 2010).…”
Section: Phenotypes Of Ren1-d Are Caused By Activation Taggingmentioning
confidence: 99%
“…2b). Both the IPT and CKX genes coexist in the moss Physcomitrella patens, which points to an important evolutionary event generating fine-tuning control of CK homeostasis via biosynthesis and degradation processes (Gu et al 2010). tRNA-IPTs are evolutionally conserved throughout the whole phylogenetic tree, whereas adenylate IPTs that are capable of de novo CK synthesis occurred later during the evolution of seed plants (Fig.…”
Section: Evolution Of Ck Machinery In Plantsmentioning
confidence: 97%
“…The algal biosynthetic pathway has not been confirmed yet, no CK-metabolic genes have been identified so far in algal genomes (Gu et al 2010), and only Type B response regulators (RRs) -but not the cytokinin receptor -have been found in the green unicellular microalgae Chlamydomonas reinhardtii (Pils and Heyl 2009). Two scenarios were suggested for the evolution of CK signalling in algae by Pils and Heyl (2009): (1) algae that were not confronted with the new stress conditions faced by the land conquesting plants and did not need more elaborate developmental programmes requiring a new or more complex regulation of CKs could have lost the CHASE domain His kinase fixed in the last common ancestor of amoebae and algae over time, or (2) CHASE domain His kinase exists in the charaphytes that are ancestral to land plants but the fact that their genome sequences have not been mapped yet has prevented the identification of CK receptors in these algae lineages.…”
Section: Evolution Of Ck Machinery In Plantsmentioning
confidence: 99%
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