Cytokinin
Cytokinins (CK) are a class of plant hormones that promote cell division, or cytokinesis, in plant roots and shoots. They are involved primarily in cell growth and differentiation, but also affect apical dominance, axillary bud growth, and leaf senescence.
There are two types of cytokinins: adenine-type cytokinins represented by
Cytokinins act in concert with auxin, another plant growth hormone. The two are complementary,[6] [7] having generally opposite effects.[2]
History
The idea of specific substances required for cell division to occur in plants actually dates back to the German physiologist
Jablonski and Skoog (1954) extended the work of Haberlandt and reported that a substance present in the vascular tissue was responsible for causing cell division in the pith cells.[11][12] Miller and his co-workers (1954) isolated and purified the cell division substance in crystallised form from autoclaved herring fish sperm DNA.[11] This active compound was named as Kinetin because of its ability to promote cell division and was the first cytokinin to be named. Kinetin was later identified to be 6-furfuryl-amino purine. Later on, the generic name kinin was suggested to include kinetin and other substances having similar properties.[8]
The first naturally occurring cytokinin was isolated and crystallised simultaneously by Miller and D.S. Lethum (1963–65) from the milky endosperm of corn (Zea mays) and named Zeatin. Lethem (1963) proposed the term Cytokinins for such substances.[13]
Function
Cytokinins are involved in many plant processes, including cell division and shoot and root morphogenesis. They are known to regulate axillary bud growth and apical dominance. According to the "direct inhibition hypothesis", these effects result from the ratio of cytokinin to auxin.[citation needed] This theory states that auxin from apical buds travels down shoots to inhibit axillary bud growth. This promotes shoot growth, and restricts lateral branching. Cytokinin moves from the roots into the shoots, eventually signaling lateral bud growth. Simple experiments support this theory. When the apical bud is removed, the axillary buds are uninhibited, lateral growth increases, and plants become bushier. Applying auxin to the cut stem again inhibits lateral dominance.[2] Moreover, it has been shown that cytokinin alone has no effect on parenchyma cells. When cultured with auxin but no cytokinin, they grow large but do not divide. When cytokinin and auxin are both added together, the cells expand and differentiate. When cytokinin and auxin are present in equal levels, the parenchyma cells form an undifferentiated callus. A higher ratio of cytokinin induces growth of shoot buds, while a higher ratio of auxin induces root formation.[2]
Cytokinins have been shown to slow aging of plant organs by preventing
Cytokinins have recently been found to play a role in plant pathogenesis. For example, cytokinins have been described to induce resistance against Pseudomonas syringae in Arabidopsis thaliana[15] and Nicotiana tabacum.[16] Also in context of biological control of plant diseases cytokinins seem to have potential functions. Production of cytokinins by Pseudomonas fluorescens G20-18 has been identified as a key determinant to efficiently control the infection of A. thaliana with P. syringae..[17]
While cytokinin action in
Mode of action
Cytokinin signaling in plants is mediated by a two-component phosphorelay. This pathway is initiated by cytokinin binding to a histidine kinase receptor in the endoplasmic reticulum membrane. This results in the autophosphorylation of the receptor, with the phosphate then being transferred to a phosphotransfer protein. The phosphotransfer proteins can then phosphorylate the type-B response regulators (RR) which are a family of transcriptions factors. The phosphorylated, and thus activated, type-B RRs regulate the transcription of numerous genes, including the type-A RRs. The type-A RRs negatively regulate the pathway.[19]
Biosynthesis
Adenosine phosphate-isopentenyltransferase (IPT)
Cytokinins can also be produced by recycled
Auxin is known to regulate the biosynthesis of cytokinin.[22]
Uses
Because cytokinins promote plant cell division and growth, they have been studied since the 1970s as potential agrochemicals, however they have yet to be widely adopted, probably due to the complex nature of their effects.[23] One study found that applying cytokinin to cotton seedlings led to a 5–10% increase in yield under drought conditions.[24] Some cytokinins are utilized in tissue culture of plants and can also be used to promote the germination of seeds.
References
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- ^ ISBN 978-1-4684-0079-3, retrieved 2022-06-17
- PMID 17729950.
- S2CID 239878163.
- ^ PMID 16009993.
- PMC 540265.
- ISBN 978-981-02-1313-8
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- ^ .
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- ^ Yao S (March 2010). "Plant Hormone Increases Cotton Yields in Drought Conditions". News & Events. Agricultural Research Service (ARS), U.S. Department of Agriculture.
External links
- Agrares Fertilizer with cytokinins
- Lincoln T, Zeiger E (2010). "Ch. 21: Cytokinins: Regulators of Cell Division". Plant Physiology (5th ed.). Sinauer. ISBN 978-0-87893-866-7.
- Plant Physiology:Cytokinin
- Regulation of Leaf Senescence by Cytokinin, Sugar, and Light