Glucose modulates proliferation in root apical meristems via TOR in maize during germination

Copyright © 2020 Elsevier Masson SAS. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Plant physiology and biochemistry : PPB. - 1991. - 155(2020) vom: 15. Okt., Seite 126-135
1. Verfasser: Díaz-Granados, Víctor Hugo (VerfasserIn)
Weitere Verfasser: López-López, Jorge Manuel, Flores-Sánchez, Jesús, Olguin-Alor, Roxana, Bedoya-López, Andrea, Dinkova, Tzvetanka D, Salazar-Díaz, Kenia, Vázquez-Santana, Sonia, Vázquez-Ramos, Jorge Manuel, Lara-Núñez, Aurora
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2020
Zugriff auf das übergeordnete Werk:Plant physiology and biochemistry : PPB
Schlagworte:Journal Article CDK Cell cycle D cyclins Germination Glucose Maize TOR IY9XDZ35W2
Beschreibung
Zusammenfassung:Copyright © 2020 Elsevier Masson SAS. All rights reserved.
The Glucose-Target of Rapamycin (Glc-TOR) pathway has been studied in different biological systems, but scarcely during early seed germination. This work examines its importance for cell proliferation, expression of cell cycle key genes, their protein levels, besides morphology and cellularization of the root apical meristem of maize (Zea mays) embryo axes during germination under the influence of two simple sugars, glucose and sucrose, and a specific inhibitor of TOR activity, AZD 8055. The two sugars promote germination similarly and to an extent, independently of TOR activity. However, the Glc-TOR pathway increases the number of cells committed to proliferation, increasing the expression of a cell cycle gene, ZmCycD4;2, a putative G1/S regulator. Also, Glc-TOR may have influence on the protein stability of another G1/S cyclin, ZmCycD3, but had no influence on ZmCDKA;1 or ZmKRP3 or their proteins. Results suggest that the Glc-TOR pathway participates in the regulation of proliferation through different mechanisms that, in the end, modify the timing of seed germination
Beschreibung:Date Completed 16.12.2020
Date Revised 16.12.2020
published: Print-Electronic
Citation Status MEDLINE
ISSN:1873-2690
DOI:10.1016/j.plaphy.2020.07.041