A protein repairing enzyme, PROTEIN L- ISOASPARTYL METHYLTRANSFERASE is involved in salinity stress tolerance by increasing efficiency of ROS-scavenging enzymes

dc.contributor.authorGhosh, Shraboni
dc.contributor.authorKamble, Nitin Uttam
dc.contributor.authorMajee, Manoj
dc.date.accessioned2020-09-21T09:58:56Z
dc.date.available2020-09-21T09:58:56Z
dc.date.issued2020
dc.descriptionAccepted date: 2 September 2020en_US
dc.description.abstractSaline conditions can significantly affect plant growth and development, leading to massive reduction in crop yield. Herein, we show that a protein repairing enzyme PROTEIN L-ISOASPARTYL METHYLTRANSFERASE imparts salinity stress tolerance in Arabidopsis thaliana by repairing deleterious isoAsp accumulation during salinity stress. We demonstrate that salinity stress accelerates isoAsp accumulation in proteins and also induces PIMT activity in Arabidopsis. Transcript analysis indicates that both PIMT1 and PIMT2 are upregulated in response to salinity stress. Subsequent functional analysis reveals that PIMT1 and PIMT2 overexpression lines are tolerant, while RNAi lines are hyper sensitive to salinity stress in comparison to wild type (WT). Biochemical analyses of thesePIMT transgenic lines also reveals that compromised salinity tolerance of RNAi lines are linked to increased isoAsp accumulation, while improved tolerance of overexpression lines is associated with reduced isoAsp accumulation in proteins. Histochemical and biochemical studies further confirm lower accumulation of ROS and reduced lipid peroxidation in PIMT overexpression lines, while increased ROS accumulation and increased lipid peroxidation in RNAi lines as compared to WT under salinity stress. Interestingly, PIMToverexpression lines exhibit improved antioxidant enzyme efficiency, while RNAi lines display compromised antioxidant enzyme efficacy as compared to WT type plants. Our study suggests that PIMT improves salinity stress tolerance by restricting salt induced-excess ROS accumulation possibly by repairing isoAsp mediated protein damage of antioxidant enzymes. Our study can be utilized for enhancing salinity stress tolerance of economically important crops.en_US
dc.description.sponsorshipThis work was supported by a grant from Department of Biotechnology (BT/PR8000/BRB/10/1210/2013), Government of India and core grant of National Institute of Plant Genome Research, New Delhi, India. SG and NUK thank University Grant Commission, Government of India and NIPGR, for research fellowship. We thank technicians of NIPGR central instrumentation facility. We thank Metabolomics facility at NIPGR for ICP-MS analysis (BT/INF/22/SP28268/2018). The authors are thankful to DBT-eLibrary Consortium (DeLCON) for providing access to e-resources.en_US
dc.identifier.citationEnvironmental and Experimental Botany, 180: 104266en_US
dc.identifier.issn0098-8472
dc.identifier.otherhttps://doi.org/10.1016/j.envexpbot.2020.104266
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0098847220302926
dc.identifier.urihttps://ndkr-library.nipgr.ac.in/handle/123456789/1097
dc.language.isoen_USen_US
dc.publisherElsevier B.V.en_US
dc.subjectSalinity stress toleranceen_US
dc.subjectPIMTen_US
dc.subjectisoAspen_US
dc.subjectROSen_US
dc.subjectAntioxidant enzymesen_US
dc.subjectArabidopsisen_US
dc.titleA protein repairing enzyme, PROTEIN L- ISOASPARTYL METHYLTRANSFERASE is involved in salinity stress tolerance by increasing efficiency of ROS-scavenging enzymesen_US
dc.typeArticleen_US

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