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Details

Autor(en) / Beteiligte
Titel
Superoxide serves as a putative signal molecule for plant cell division: overexpression of CaRLK1 promotes the plant cell cycle via accumulation of O2− and decrease in H2O2
Ist Teil von
  • Physiologia plantarum, 2017-02, Vol.159 (2), p.228-243
Ort / Verlag
Oxford, UK: Blackwell Publishing Ltd
Erscheinungsjahr
2017
Quelle
Wiley Online Library Journals Frontfile Complete
Beschreibungen/Notizen
  • Reactive oxygen species (ROS) exert both positive and negative effects on plant growth and development and therefore receive a great deal of attention in current research. A hot pepper, Capsicum annuum receptor‐like kinase 1 (CaRLK1) was ectopically expressed in Nicotiana tabacum BY‐2 cell and Nicotiana benthamiana plants. This ectopic expression of CaRLK1 enhanced cell division and proliferation in both heterologous systems. Apparently, CaRLK1 is involved in controlling the cell cycle, possibly by inducing expressions of cyclin B1, cyclin D3, cyclin‐dependent protein kinase 3, condensin complex subunit 2 and anaphase‐promoting complex subunit 11 genes. CaRLK1 overexpression also increased transcript accumulation of NADPH oxidase genes, generation of O2− and catalase (CAT) activity/protein levels. In parallel, it decreased cellular H2O2 levels and cell size. Treatment with Tiron or diphenyleneiodonium (DPI) both decreased the cell division rate and O2− concentrations, but increased cellular H2O2 levels. Tobacco BY‐2 cells overexpressing CaRLK1 were more sensitive to amino‐1,2,4‐triazole (3‐AT), a CAT inhibitor, than control cells, suggesting that the increased H2O2 levels may not function as a signal for cell division and proliferation. Overexpression of CaRLK1 stimulated progression of the cell cycle from G0/G1 phase into the S phase. It is concluded that the CaRLK1 protein plays a pivotal role in controlling the level of O2− as signaling molecule which promotes cell division, concomitant with a reduction in H2O2 by the induction of CAT activity/protein.
Sprache
Englisch
Identifikatoren
ISSN: 0031-9317
eISSN: 1399-3054
DOI: 10.1111/ppl.12487
Titel-ID: cdi_proquest_journals_1858574777
Format
Schlagworte
Cell cycle, Cell division, Kinases, Proteins

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