scholarly journals Characterization of the Glehnia littoralis Non-specific Phospholipase C Gene GlNPC3 and Its Involvement in the Salt Stress Response

2021 ◽  
Vol 12 ◽  
Author(s):  
Li Li ◽  
Naiwei Li ◽  
Xiwu Qi ◽  
Yang Bai ◽  
Qiutong Chen ◽  
...  

Glehnia littoralis is a medicinal halophyte that inhabits sandy beaches and has high ecological and commercial value. However, the molecular mechanism of salt adaptation in G. littoralis remains largely unknown. Here, we cloned and identified a non-specific phospholipase C gene (GlNPC3) from G. littoralis, which conferred lipid-mediated signaling during the salt stress response. The expression of GlNPC3 was induced continuously by salt treatment. Overexpression of GlNPC3 in Arabidopsis thaliana increased salt tolerance compared to wild-type (WT) plants. GlNPC3-overexpressing plants had longer roots and higher fresh and dry masses under the salt treatment. The GlNPC3 expression pattern revealed that the gene was expressed in most G. littoralis tissues, particularly in roots. The subcellular localization of GlNPC3 was mainly at the plasma membrane, and partially at the tonoplast. GlNPC3 hydrolyzed common membrane phospholipids, such as phosphotidylserine (PS), phosphoethanolamine (PE), and phosphocholine (PC). In vitro enzymatic assay showed salt-induced total non-specific phospholipase C (NPC) activation in A. thaliana GlNPC3-overexpressing plants. Plant lipid profiling showed a significant change in the membrane-lipid composition of A. thaliana GlNPC3-overexpressing plants compared to WT after the salt treatment. Furthermore, downregulation of GlNPC3 expression by virus-induced gene silencing in G. littoralis reduced the expression levels of some stress-related genes, such as SnRK2, P5SC5, TPC1, and SOS1. Together, these results indicated that GlNPC3 and GlNPC3-mediated membrane lipid change played a positive role in the response of G. littoralis to a saline environment.

Author(s):  
Cecilia Eugenia María Grossi ◽  
Franco Santin ◽  
Silverio Andrés Quintana ◽  
Elisa Fantino ◽  
Rita María Ulloa

2021 ◽  
Vol 329 ◽  
pp. 180-191
Author(s):  
Ulkar İbrahimova ◽  
Pragati Kumari ◽  
Saurabh Yadav ◽  
Anshu Rastogi ◽  
Michal Antala ◽  
...  

BMC Genomics ◽  
2012 ◽  
Vol 13 (1) ◽  
pp. 215 ◽  
Author(s):  
Guido Mastrobuoni ◽  
Susann Irgang ◽  
Matthias Pietzke ◽  
Heike E Aßmus ◽  
Markus Wenzel ◽  
...  

2007 ◽  
Vol 27 (22) ◽  
pp. 7771-7780 ◽  
Author(s):  
Paul E. Verslues ◽  
Giorgia Batelli ◽  
Stefania Grillo ◽  
Fernanda Agius ◽  
Yong-Sig Kim ◽  
...  

ABSTRACT SOS2, a class 3 sucrose-nonfermenting 1-related kinase, has emerged as an important mediator of salt stress response and stress signaling through its interactions with proteins involved in membrane transport and in regulation of stress responses. We have identified additional SOS2-interacting proteins that suggest a connection between SOS2 and reactive oxygen signaling. SOS2 was found to interact with the H2O2 signaling protein nucleoside diphosphate kinase 2 (NDPK2) and to inhibit its autophosphorylation activity. A sos2-2 ndpk2 double mutant was more salt sensitive than a sos2-2 single mutant, suggesting that NDPK2 and H2O2 are involved in salt resistance. However, the double mutant did not hyperaccumulate H2O2 in response to salt stress, suggesting that it is altered signaling rather than H2O2 toxicity alone that is responsible for the increased salt sensitivity of the sos2-2 ndpk2 double mutant. SOS2 was also found to interact with catalase 2 (CAT2) and CAT3, further connecting SOS2 to H2O2 metabolism and signaling. The interaction of SOS2 with both NDPK2 and CATs reveals a point of cross talk between salt stress response and other signaling factors including H2O2.


2021 ◽  
Author(s):  
Ashok Saddhe Ankush ◽  
Ajay Kumar Mishra ◽  
Kumar Kundan

2018 ◽  
Vol 132 (2) ◽  
pp. 323-346 ◽  
Author(s):  
Benedict C. Oyiga ◽  
Francis C. Ogbonnaya ◽  
Ram C. Sharma ◽  
Michael Baum ◽  
Jens Léon ◽  
...  

2017 ◽  
Vol 94 (4-5) ◽  
pp. 531-548 ◽  
Author(s):  
Hung-Chi Chen ◽  
Vicki Hsieh-Feng ◽  
Pei-Chun Liao ◽  
Wan-Hsing Cheng ◽  
Li-Yu Liu ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document