4.7 Article

CsGSTU8, a Glutathione S-Transferase From Camellia sinensis, Is Regulated by CsWRKY48 and Plays a Positive Role in Drought Tolerance

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FRONTIERS IN PLANT SCIENCE
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fpls.2021.795919

关键词

Camellia sinensis; glutathione S-transferases (GSTs); ROS; WRKY TF; drought stress

资金

  1. China Agriculture Research System of MOF and MARA [CARS-19]
  2. Agricultural Special Fund Project of Shaanxi Province [NYKJ-2020-YL-13]
  3. Key RAMP
  4. D Program of Shaanxi Province [2020LSFP3-16]
  5. special fund for University-Supported Extension Model [XTG2021-04]

向作者/读者索取更多资源

The study demonstrates that in tea plants, the CsGSTU8 gene is upregulated in response to drought stress and ABA treatment, playing a critical role in enhancing drought tolerance. It also reveals that CsWRKY48 functions as a transcriptional activator and activates the expression of CsGSTU8, providing new insights into drought stress responses in tea plants.
Glutathione S-transferases (GSTs) constitute a large family of enzymes with a wide range of cellular functions. Recently, plant GSTs have gained a great deal of attention due to their involvement in the detoxification of electrophilic xenobiotics and peroxides under adverse environmental conditions, such as salt, cold, UV-B and drought stress. A previous study reported that a GST gene (CsGSTU8) in tea plant was distinctly induced in response to drought, suggesting this gene plays a critical role in the drought stress response. In this study, by using quantitative real-time PCR (qRT-PCR) and beta-glucuronidase (GUS) reporter lines, we further demonstrated that CsGSTU8 was upregulated in response to drought stress and exogenous abscisic acid (ABA) treatments. Overexpression of CsGSTU8 in Arabidopsis resulted in enhanced drought tolerance as indicated by the improved scavenging of excess amounts of reactive oxygen species (ROS) under drought conditions. Furthermore, we found that CsWRKY48 acts as a transcriptional activator and that its expression is induced in response to drought stress and ABA treatment. Electrophoretic mobility shift assays (EMSAs), dual-luciferase (LUC) assays and transient expression assays in tea plant leaves revealed that CsWRKY48 directly binds to the W-box elements in the promoter of CsGSTU8 and activates its expression. Taken together, our results provide additional knowledge of drought stress responses in tea plant.

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