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Dive into the research topics where Sumita Kumari is active.

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Featured researches published by Sumita Kumari.


Functional & Integrative Genomics | 2009

Transcriptome map for seedling stage specific salinity stress response indicates a specific set of genes as candidate for saline tolerance in Oryza sativa L.

Sumita Kumari; Vaishali Panjabi nee Sabharwal; Hemant R. Kushwaha; Sudhir K. Sopory; Sneh L. Singla-Pareek; Ashwani Pareek

Oryza sativa L. cv IR64 is a widely cultivated, salt-sensitive indica rice, while Pokkali is a well-known, naturally salt-tolerant relative. To understand the molecular basis of differences in their salinity tolerance, three subtractive cDNA libraries were constructed. A total of 1,194 salinity-regulated cDNAs are reported here that may serve as repositories for future individual gene-based functional genomics studies. Gene expression data using macroarrays and Northern blots gives support to our hypothesis that salinity tolerance of Pokkali may be due to constitutive overexpression of many genes that function in salinity tolerance and are stress inducible in IR64. Analysis of genome architecture revealed the presence of these genes on all the chromosomes with several distinct clusters. Notably, a few mapped on one of the major quantitative trait loci – Saltol – on chromosome 1 and were found to be differentially regulated in the two contrasting genotypes. The present study also defines a set of known abiotic stress inducible genes, including CaMBP, GST, LEA, V-ATPase, OSAP1 zinc finger protein, and transcription factor HBP1B, that were expressed at high levels in Pokkali even in the absence of stress. These proposed genes may prove useful as “candidates” in improving salinity tolerance in crop plants using transgenic approach.


Plant Signaling & Behavior | 2013

Cyclophilins: Proteins in search of function

Sumita Kumari; Suchismita Roy; Prabhjeet Singh; Sneh L. Singla-Pareek; Ashwani Pareek

Cyclophilins constitute a subgroup of large family of proteins called immunophilins, which also include FKBPs and Parvulins. They are remarkably conserved in all genera, highlighting their pivotal role in important cellular processes. Most cyclophilins display PPIase enzymatic activity, multiplicity, diverse cellular locations and active role in protein folding which render them to be included in the class of diverse set of proteins called molecular chaperones. Due to their distinct PPIase function, besides protein disulfide isomerases and protein foldases, cyclophilins have been deemed necessary for in vivo chaperoning activity. Unlike other cellular chaperones, these proteins are specific in their respective targets. Not all cyclophilin proteins possess PPIase activity, indicating a loss of their PPIase activity during the course of evolution and gain of function independent of their PPIase activity. The PPIase function of cyclophilins is also compensated by their functional homologs, like FKBPs. Multiple cyclophilin members in plants like Arabidopsis and rice have been reported to be associated with diverse functions and regulatory pathways through their foldase, scaffolding, chaperoning or other unknown activities. Although many functions of plant cyclophilins were reported or suggested, the physiological relevance and molecular basis of stress-responsive expression of plant cyclophilins is still largely unknown. However, their wide distribution and ubiquitous nature signifies their fundamental importance in plant survival. Several of these members have also been directly linked to multiple stresses. This review attempts to deal with plant cyclophilins with respect to their role in stress response.


BMC Plant Biology | 2012

Clustered metallothionein genes are co-regulated in rice and ectopic expression of OsMT1e-P confers multiple abiotic stress tolerance in tobacco via ROS scavenging

Gautam Kumar; Hemant R. Kushwaha; Vaishali Panjabi-Sabharwal; Sumita Kumari; Rohit Joshi; Ratna Karan; Shweta Mittal; Sneh L Singla Pareek; Ashwani Pareek

BackgroundMetallothioneins (MT) are low molecular weight, cysteine rich metal binding proteins, found across genera and species, but their function(s) in abiotic stress tolerance are not well documented.ResultsWe have characterized a rice MT gene, OsMT1e-P, isolated from a subtractive library generated from a stressed salinity tolerant rice genotype, Pokkali. Bioinformatics analysis of the rice genome sequence revealed that this gene belongs to a multigenic family, which consists of 13 genes with 15 protein products. OsMT1e-P is located on chromosome XI, away from the majority of other type I genes that are clustered on chromosome XII. Various members of this MT gene cluster showed a tight co-regulation pattern under several abiotic stresses. Sequence analysis revealed the presence of conserved cysteine residues in OsMT1e-P protein. Salinity stress was found to regulate the transcript abundance of OsMT1e-P in a developmental and organ specific manner. Using transgenic approach, we found a positive correlation between ectopic expression of OsMT1e-P and stress tolerance. Our experiments further suggest ROS scavenging to be the possible mechanism for multiple stress tolerance conferred by OsMT1e-P.ConclusionWe present an overview of MTs, describing their gene structure, genome localization and expression patterns under salinity and development in rice. We have found that ectopic expression of OsMT1e-P enhances tolerance towards multiple abiotic stresses in transgenic tobacco and the resultant plants could survive and set viable seeds under saline conditions. Taken together, the experiments presented here have indicated that ectopic expression of OsMT1e-P protects against oxidative stress primarily through efficient scavenging of reactive oxygen species.


Functional & Integrative Genomics | 2015

Expression of a cyclophilin OsCyp2-P isolated from a salt-tolerant landrace of rice in tobacco alleviates stress via ion homeostasis and limiting ROS accumulation

Sumita Kumari; Rohit Joshi; Kushwant Singh; Suchismita Roy; Amit K. Tripathi; Prabhjeet Singh; Sneh L. Singla-Pareek; Ashwani Pareek

Cyclophilins are a set of ubiquitous proteins present in all subcellular compartments, involved in a wide variety of cellular processes. Comparative bioinformatics analysis of the rice and Arabidopsis genomes led us to identify novel putative cyclophilin gene family members in both the genomes not reported previously. We grouped cyclophilin members with similar molecular weight and subtypes together in the phylogenetic tree which indicated their co-evolution in rice and Arabidopsis. We also characterized a rice cyclophilin gene, OsCyp2-P (Os02g0121300), isolated from a salinity-tolerant landrace, Pokkali. Publicly available massively parallel signature sequencing (MPSS) and microarray data, besides our quantitative real time PCR (qRT-PCR) data suggest that transcript abundance of OsCyp2-P is regulated under different stress conditions in a developmental and organ specific manner. Ectopic expression of OsCyp2-P imparted multiple abiotic stress tolerance to transgenic tobacco plants as evidenced by higher root length, shoot length, chlorophyll content, and K+/Na+ ratio under stress conditions. Transgenic plants also showed reduced lipid peroxidase content, electrolyte leakage, and superoxide content under stress conditions suggesting better ion homeostasis than WT plants. Localization studies confirmed that OsCyp2-P is localized in both cytosol and nucleus, indicating its possible interaction with several other proteins. The overall results suggest the explicit role of OsCyp2-P in bestowing multiple abiotic stress tolerance at the whole plant level. OsCyp2-P operates via reactive oxygen species (ROS) scavenging and ion homeostasis and thus is a promising candidate gene for enhancing multiple abiotic stress tolerance in crop plants.


PLOS ONE | 2016

Arabidopsis thaliana Contains Both Ni2+ and Zn2+ Dependent Glyoxalase I Enzymes and Ectopic Expression of the Latter Contributes More towards Abiotic Stress Tolerance in E. coli

Muskan Jain; Rituraj Batth; Sumita Kumari; Ananda Mustafiz

The glyoxalase pathway is ubiquitously found in all the organisms ranging from prokaryotes to eukaryotes. It acts as a major pathway for detoxification of methylglyoxal (MG), which deleteriously affects the biological system in stress conditions. The first important enzyme of this system is Glyoxalase I (GLYI). It is a metalloenzyme which requires divalent metal ions for its activity. This divalent metal ion can be either Zn2+ as found in most of eukaryotes or Ni2+ as seen in prokaryotes. In the present study, we have found three active GLYI enzymes (AtGLYI2, AtGLYI3 and AtGLYI6) belonging to different metal activation classes coexisting in Arabidopsis thaliana. These enzymes have been found to efficiently complement the GLYI yeast mutants. These three enzymes have been characterized in terms of their activity, metal dependency, kinetic parameters and their role in conferring tolerance to multiple abiotic stresses in E. coli and yeast. AtGLYI2 was found to be Zn2+ dependent whereas AtGLYI3 and AtGLYI6 were Ni2+ dependent. Enzyme activity of Zn2+ dependent enzyme, AtGLYI2, was observed to be exceptionally high (~250–670 fold) as compared to Ni2+ dependent enzymes, AtGLYI3 and AtGLYI6. The activity of these GLYI enzymes correlated well to their role in stress tolerance. Heterologous expression of these enzymes in E. coli led to better tolerance against various stress conditions. This is the first report of a higher eukaryotic species having multiple active GLYI enzymes belonging to different metal activation classes.


Frontiers in Plant Science | 2017

Transcript Profiling Reveals the Presence of Abiotic Stress and Developmental Stage Specific Ascorbate Oxidase Genes in Plants

Rituraj Batth; Kapil Singh; Sumita Kumari; Ananda Mustafiz

Abiotic stress and climate change is the major concern for plant growth and crop yield. Abiotic stresses lead to enhanced accumulation of reactive oxygen species (ROS) consequently resulting in cellular damage and major losses in crop yield. One of the major scavengers of ROS is ascorbate (AA) which acts as first line of defense against external oxidants. An enzyme named ascorbate oxidase (AAO) is known to oxidize AA and deleteriously affect the plant system in response to stress. Genome-wide analysis of AAO gene family has led to the identification of five, three, seven, four, and six AAO genes in Oryza sativa, Arabidopsis, Glycine max, Zea mays, and Sorghum bicolor genomes, respectively. Expression profiling of these genes was carried out in response to various abiotic stresses and during various stages of vegetative and reproductive development using publicly available microarray database. Expression analysis in Oryza sativa revealed tissue specific expression of AAO genes wherein few members were exclusively expressed in either root or shoot. These genes were found to be regulated by both developmental cues as well as diverse stress conditions. The qRT-PCR analysis in response to salinity and drought stress in rice shoots revealed OsAAO2 to be the most stress responsive gene. On the other hand, OsAAO3 and OsAAO4 genes showed enhanced expression in roots under salinity/drought stresses. This study provides lead about important stress responsive AAO genes in various crop plants, which could be used to engineer climate resilient crop plants.


Acta Crystallographica Section D-biological Crystallography | 2013

Structural and biochemical characterization of the cytosolic wheat cyclophilin TaCypA-1.

Simranjeet Singh Sekhon; Harsimran Kaur; Tanima Dutta; Khushwant Singh; Sumita Kumari; Sunghyun Kang; Sung Goo Park; Byoung Chul Park; Dae Gwin Jeong; Ashwani Pareek; Eui-Jeon Woo; Prabhjeet Singh; Tae-Sung Yoon

Cyclophilins belong to a family of proteins that bind to the immunosuppressive drug cyclosporin A (CsA). Several members of this protein family catalyze the cis-trans isomerization of peptide bonds preceding prolyl residues. The present study describes the biochemical and structural characteristics of a cytosolic cyclophilin (TaCypA-1) cloned from wheat (Triticum aestivum L.). Purified TaCypA-1 expressed in Escherichia coli showed peptidyl-prolyl cis-trans isomerase activity, which was inhibited by CsA with an inhibition constant of 78.3 nM. The specific activity and catalytic efficiency (kcat/Km) of the purified TaCypA-1 were 99.06 ± 0.13 nmol s(-1) mg(-1) and 2.32 × 10(5) M(-1) s(-1), respectively. The structures of apo TaCypA-1 and the TaCypA-1-CsA complex were determined at 1.25 and 1.20 Å resolution, respectively, using X-ray diffraction. Binding of CsA to the active site of TaCypA-1 did not result in any significant conformational change in the apo TaCypA-1 structure. This is consistent with the crystal structure of the human cyclophilin D-CsA complex reported at 0.96 Å resolution. The TaCypA-1 structure revealed the presence of a divergent loop of seven amino acids (48)KSGKPLH(54) which is a characteristic feature of plant cyclophilins. This study is the first to elucidate the structure of an enzymatically active plant cyclophilin which shows peptidyl-prolyl cis-trans isomerase activity and the presence of a divergent loop.


Archive | 2017

Glyoxalase System: A Glutathione-Dependent Pathway for Abiotic Stress Tolerance in Plants

Rituraj Batth; Muskan Jain; Sumita Kumari; Ananda Mustafiz

Due to their sessile nature, plants have to go through various adverse environmental conditions. Abiotic stresses, such as salinity, drought, flooding, cold, heat, etc. have been the major environmental factors contributing to the decreased yield of important crop plants. Abiotic stress leads to an abrupt increase in the contents of methylglyoxal (MG) in plants. MG is a potent cytotoxin, and readily reacts with major macromolecules of the cell to form advanced glycation end-products (AGEs ). MG detoxification is principally carried out by the glyoxalase (GLY) system, which consists of two enzymes, GLYI and GLYII. GLYI acts upon the non-enzymatically formed complex of MG and a molecule of reduced glutathione (GSH), leading to the production of S-D-lactoylglutathione (SLG). GLYII, then, catalyzes the conversion of SLG to D-lactate giving GSH back to the system, thereby maintaining GSH homeostasis. The glyoxalase pathway keeps a check on the elevation of the MG level and helps in maintaining a higher “reduced to oxidized” GSH ratio. The glyoxalase pathway has been directly correlated to abiotic stress tolerance. Overexpression of GLY enzymes confers improved abiotic stress tolerance in plants. This chapter provides insights into the importance of the glyoxalase pathway in stress response and sheds light on the dependence of the glyoxalase pathway on GSH as the key player in regulating the pathway.


Scientific Reports | 2018

GLYI and D-LDH play key role in methylglyoxal detoxification and abiotic stress tolerance

Muskan Jain; Preeti Nagar; Ayush Sharma; Rituraj Batth; Sakshi Aggarwal; Sumita Kumari; Ananda Mustafiz

Methylglyoxal(MG) is a potent cytotoxin that is produced as a byproduct of various metabolic reactions in the cell. The major enzymes for MG detoxification are Glyoxalase I(GLYI), Glyoxalase II(GLYII) and D-lactate dehydrogenase(D-LDH). These three enzymes work together and convert MG into D-pyruvate, which directly goes to TCA cycle. Here, a comparative study of the ability of MG detoxification of these three enzymes has been done in both E. coli and yeast. Ectopic expression of these three genes from Arabidopsis in E. coli in presence of different abiotic stress revealed the contribution of each of these genes in detoxifying MG. Yeast mutants of MG detoxification enzymes were also grown in different stress conditions to record the effect of each gene. These mutants were also used for complementation assays using the respective MG detoxifying genes from Arabidopsis in presence of various stress conditions. The MG content and the corresponding growth of cells was measured in all the bacterial as well as yeast strains. This study reveals differential contribution of MG detoxification enzymes in mitigating MG levels and alleviating stress in both prokaryotes as well as eukaryotes. GLYI and D-LDH were found to be key enzymes in MG detoxification under various abiotic stresses.


Archive | 2018

Second Messengers: Central Regulators in Plant Abiotic Stress Response

Muskan Jain; Preeti Nagar; Parul Goel; Anil Kumar Singh; Sumita Kumari; Ananda Mustafiz

Plants differ from animals by lacking the ability to escape from their environmental conditions. Plants adapt to the seasonal as well as nonseasonal perturbations by means of stress-responsive genes. Manipulation of such genes has been shown to provide abiotic stress tolerance in plants. Since abiotic stress is a polygenic trait, overexpression of single stress-responsive gene would not serve the purpose of getting stress-tolerant plants. So, the focus needs to be shifted towards the “master regulators” which are critical for plant growth and development and play an important role in integrating various stress signals and controlling downstream stress responses by modulating gene expression machinery. In plants, there are various second messengers including calcium, ROS, phosphoinositides, cyclic nucleotides, etc., which are known to initiate the downstream signaling cascade leading to response against different, multiple, and simultaneous ambient cues. A better understanding of these elements will allow us to engineer a particular stress-responsive pathway, to achieve better stress-tolerant plants.

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Ashwani Pareek

Jawaharlal Nehru University

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Prabhjeet Singh

Guru Nanak Dev University

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Muskan Jain

South Asian University

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Sneh L. Singla-Pareek

International Centre for Genetic Engineering and Biotechnology

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Jebi Sudan

Sher-e-Kashmir University of Agricultural Sciences and Technology of Jammu

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Harsimran Kaur

Jawaharlal Nehru University

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Hemant R. Kushwaha

Jawaharlal Nehru University

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