102-1 Response of Microtubule Arrays and Ca2+ Signal Transduction in Sugarcane Cultivars of Different Tolerance to Cold Stress.

Poster Number 309

See more from this Division: C02 Crop Physiology and Metabolism
See more from this Session: Stress Physiology

Monday, November 4, 2013
Tampa Convention Center, East Exhibit Hall

Suli Li, Agronomy Deparment, Guangxi University, Nanning, China, Zhigang Li, University of Florida Indian River Research & Education Center, Fort Pierce, FL, Litao Yang, State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guanxi University, Nanning, China and Zhenli He, Indian River Research and Education Center, Institute of Food and Agricultural Sciences, University of Florida, Fort Pierce, FL
Abstract:
Microtubules are an important component of cells and their rearrangement is closely related to Ca2+ concentration of cell signal transduction under cold stress.  An investigation was conducted in two sugarcane cultivars, GT28 (cold-tolerance) and YL6 (cold-susceptible) to better understand the relationship between the cytoskeleton and signaling of cold stress. Two different temperature regimes were used (0°C, cold stress and 25°C, control) and the plants at early ripening stage were exposed to cold-stress for 6 days. The results showed: (1) before cold stress, the cortical microtubule arrays were mainly oriented transversely to the elongation axis and orderly structured in the cells for both sugarcane cultivars, though the microtubule arrays were more densely structured in GT28 than in YL6. After cold stress, the microtubules in YL6 were disarrayed due to depolymerization and condensation, and the cell boundary became indistinct, while the cortical microtubule arrays in GT28 were re-ordered, re-oriented in all directions after depolymerization, and thus became more densely  arranged; (2) both sugarcane cultivars accumulated Ca2+ pellets in cytoplasm and nucleolus at the beginning of cold stress, but Ca2+ pellets in GT28 decreased and maintained at a low level while they were maintained at a high level in YL6 with the extension of cold stress. (3) Cold stress had a minimal influence on Ca2+-ATPase activity and its distribution in GT28, which was maintained at a high level. On the contrary, Ca2+-ATPase activity in YL6 was reduced with extended cold stress. It suggests that a high level of Ca2+ in cytoplasm is one of the important reasons for cell injury from cold for the cold sensitive cultivars, while high Ca2+-ATPase activity mitigates such effect by reducing Ca2+ accumulation in cytoplasm, thus rendering the microtubule arrays more acclimatized to cold stress for the cold tolerant cultivars of sugarcane.

See more from this Division: C02 Crop Physiology and Metabolism
See more from this Session: Stress Physiology

Previous Abstract | Next Abstract >>