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Recapitulation of the Function and Role of ROS Generated in Response to Heat Stress in Plants

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Journal Plants (Basel)
Date 2021 Mar 6
PMID 33671904
Citations 43
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Abstract

In natural ecosystems, plants are constantly exposed to changes in their surroundings as they grow, caused by a lifestyle that requires them to live where their seeds fall. Thus, plants strive to adapt and respond to changes in their exposed environment that change every moment. Heat stress that naturally occurs when plants grow in the summer or a tropical area adversely affects plants' growth and poses a risk to plant development. When plants are subjected to heat stress, they recognize heat stress and respond using highly complex intracellular signaling systems such as reactive oxygen species (ROS). ROS was previously considered a byproduct that impairs plant growth. However, in recent studies, ROS gained attention for its function as a signaling molecule when plants respond to environmental stresses such as heat stress. In particular, ROS, produced in response to heat stress in various plant cell compartments such as mitochondria and chloroplasts, plays a crucial role as a signaling molecule that promotes plant growth and triggers subsequent downstream reactions. Therefore, this review aims to address the latest research trends and understandings, focusing on the function and role of ROS in responding and adapting plants to heat stress.

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References
1.
Choi H, Kim S, Mukhopadhyay P, Cho S, Woo J, Storz G . Structural basis of the redox switch in the OxyR transcription factor. Cell. 2001; 105(1):103-13. DOI: 10.1016/s0092-8674(01)00300-2. View

2.
Prasad P, Craufurd P, Summerfield R, Wheeler T . Effects of short episodes of heat stress on flower production and fruit-set of groundnut (Arachis hypogaea L.). J Exp Bot. 2000; 51(345):777-84. DOI: 10.1093/jexbot/51.345.777. View

3.
Mittler R, Vanderauwera S, Suzuki N, Miller G, Tognetti V, Vandepoele K . ROS signaling: the new wave?. Trends Plant Sci. 2011; 16(6):300-9. DOI: 10.1016/j.tplants.2011.03.007. View

4.
Pospisil P . Production of Reactive Oxygen Species by Photosystem II as a Response to Light and Temperature Stress. Front Plant Sci. 2017; 7:1950. PMC: 5183610. DOI: 10.3389/fpls.2016.01950. View

5.
Poltronieri P, Santino A . Non-coding RNAs in Intercellular and Systemic Signaling. Front Plant Sci. 2012; 3:141. PMC: 3389742. DOI: 10.3389/fpls.2012.00141. View