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A cassava drought inducible CC-type glutaredoxin, MeGRX232 , negatively regulates drought tolerance in Arabidopsis by inhibition of ABA-dependent stomatal closure

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s00299-007-0378-8openalex-snapshot

Characterization of an 18,166 EST dataset for cassava (Manihot esculenta Crantz) enriched for drought-responsive genes

inferredcites →https://doi.org/10.1007/s00299-013-1418-1openalex-snapshot

ABA signaling in stress-response and seed development

inferredcites →https://doi.org/10.1007/s00425-013-1940-yopenalex-snapshot

Modified expression of an auxin-responsive rice CC-type glutaredoxin gene affects multiple abiotic stress responses

inferredcites →https://doi.org/10.1007/s10265-011-0412-3openalex-snapshot

ABA-mediated transcriptional regulation in response to osmotic stress in plants

inferredcites →https://doi.org/10.1007/s11033-011-0823-1openalex-snapshot

Signal transduction during cold, salt, and drought stresses in plants

inferredcites →https://doi.org/10.1016/j.bbrc.2010.11.050openalex-snapshot

Engineered mutated glutaredoxins mimicking peculiar plant class III glutaredoxins bind iron–sulfur centers and possess reductase activity

inferredcites →https://doi.org/10.1016/j.plantsci.2015.05.011openalex-snapshot

Rice OsiSAP7 negatively regulates ABA stress signalling and imparts sensitivity to water-deficit stress in Arabidopsis

inferredcites →https://doi.org/10.1038/35021067openalex-snapshot

Calcium channels activated by hydrogen peroxide mediate abscisic acid signalling in guard cells

inferredcites →https://doi.org/10.1038/srep21542openalex-snapshot

Reactive oxygen species regulate leaf pulvinus abscission zone cell separation in response to water-deficit stress in cassava

inferredcites →https://doi.org/10.1038/srep22783openalex-snapshot

Genome-wide characterization and analysis of bZIP transcription factor gene family related to abiotic stress in cassava

inferredcites →https://doi.org/10.1046/j.0016-8025.2001.00824.xopenalex-snapshot

ABA‐based chemical signalling: the co‐ordination of responses to stress in plants

inferredcites →https://doi.org/10.1046/j.1365-313x.1997.11061187.xopenalex-snapshot

Subcellular localization of H2O2 in plants. H2O2 accumulation in papillae and hypersensitive response during the barley—powdery mildew interaction

inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot

Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana

inferredcites →https://doi.org/10.1073/pnas.0702268104openalex-snapshot

Functional, structural, and spectroscopic characterization of a glutathione-ligated [2Fe–2S] cluster in poplar glutaredoxin C1

inferredcites →https://doi.org/10.1074/jbc.m111.228726openalex-snapshot

Arabidopsis Chloroplastic Glutaredoxin C5 as a Model to Explore Molecular Determinants for Iron-Sulfur Cluster Binding into Glutaredoxins

inferredcites →https://doi.org/10.1074/jbc.m600138200openalex-snapshot

The Effects of Glutaredoxin and Copper Activation Pathways on the Disulfide and Stability of Cu,Zn Superoxide Dismutase

inferredcites →https://doi.org/10.1074/jbc.m604359200openalex-snapshot

Glutaredoxin Modulates Platelet-derived Growth Factor-dependent Cell Signaling by Regulating the Redox Status of Low Molecular Weight Protein-tyrosine Phosphatase

inferredcites →https://doi.org/10.1089/ars.2011.4327openalex-snapshot

Thioredoxin and Glutaredoxin Systems in Plants: Molecular Mechanisms, Crosstalks, and Functional Significance

inferredcites →https://doi.org/10.1093/aob/mch179openalex-snapshot

Response of Cassava Leaf Area Expansion to Water Deficit: Cell Proliferation, Cell Expansion and Delayed Development

inferredcites →https://doi.org/10.1093/dnares/dsq023openalex-snapshot

Genome-Wide Survey and Expression Analysis Suggest Diverse Roles of Glutaredoxin Gene Family Members During Development and Response to Various Stimuli in Rice

inferredcites →https://doi.org/10.1093/gbe/evp025openalex-snapshot

Origin and Diversification of Land Plant CC-Type Glutaredoxins

inferredcites →https://doi.org/10.1093/jexbot/53.366.33openalex-snapshot

ABA, ethylene and the control of shoot and root growth under water stress

inferredcites →https://doi.org/10.1093/jxb/erl001openalex-snapshot

Genome-wide analysis of plant glutaredoxin systems

inferredcites →https://doi.org/10.1093/jxb/err301openalex-snapshot

Glutaredoxin GRXS13 plays a key role in protection against photooxidative stress in Arabidopsis

inferredcites →https://doi.org/10.1093/jxb/ers389openalex-snapshot

TGA transcription factors and jasmonate-independent COI1 signalling regulate specific plant responses to reactive oxylipins

inferredcites →https://doi.org/10.1093/jxb/eru507openalex-snapshot

Analysis of different strategies adapted by two cassava cultivars in response to drought stress: ensuring survival or continuing growth

inferredcites →https://doi.org/10.1093/molbev/msr121openalex-snapshot

MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods

inferredcites →https://doi.org/10.1093/mp/ssn078openalex-snapshot

Conserved Functions of Arabidopsis and Rice CC-Type Glutaredoxins in Flower Development and Pathogen Response

inferredcites →https://doi.org/10.1093/mp/ssr113openalex-snapshot

Repression of the Arabidopsis thaliana Jasmonic Acid/Ethylene-Induced Defense Pathway by TGA-Interacting Glutaredoxins Depends on Their C-Terminal ALWL Motif

inferredcites →https://doi.org/10.1093/nar/22.22.4673openalex-snapshot

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

inferredcites →https://doi.org/10.1104/pp.106.095299openalex-snapshot

Genetic Interactions of TGA Transcription Factors in the Regulation of Pathogenesis-Related Genes and Disease Resistance in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.111.185199openalex-snapshot

The ROXY1 C-Terminal L**LL Motif Is Essential for the Interaction with TGA Transcription Factors

inferredcites →https://doi.org/10.1104/pp.112.212803openalex-snapshot

Enhanced Reactive Oxygen Species Scavenging by Overproduction of Superoxide Dismutase and Catalase Delays Postharvest Physiological Deterioration of Cassava Storage Roots

inferredcites →https://doi.org/10.1105/tpc.108.064477openalex-snapshot

Nuclear Activity of ROXY1, a Glutaredoxin Interacting with TGA Factors, Is Required for Petal Development inArabidopsis thaliana

inferredcites →https://doi.org/10.1105/tpc.111.093740openalex-snapshot

Somatic and Reproductive Cell Development in Rice Anther Is Regulated by a Putative Glutaredoxin

inferredcites →https://doi.org/10.1111/j.1365-3040.2011.02383.xopenalex-snapshot

Differential response of young and adult leaves to herbicide 2,4‐dichlorophenoxyacetic acid in pea plants: role of reactive oxygen species

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02593.xopenalex-snapshot

Methods and concepts in quantifying resistance to drought, salt and freezing, abiotic stresses that affect plant water status

inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03039.xopenalex-snapshot

SA‐inducible Arabidopsis glutaredoxin interacts with TGA factors and suppresses JA‐responsive PDF1.2 transcription

inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03375.xopenalex-snapshot

ROXY1 and ROXY2, two Arabidopsis glutaredoxin genes, are required for anther development

inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04044.xopenalex-snapshot

Arabidopsis thaliana class-II TGA transcription factors are essential activators of jasmonic acid/ethylene-induced defense responses

inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04706.xopenalex-snapshot

The glutaredoxin ATGRXS13 is required to facilitate Botrytis cinerea infection of Arabidopsis thaliana plants

inferredcites →https://doi.org/10.1186/1471-2164-13-64openalex-snapshot

Transcriptome profiling of low temperature-treated cassava apical shoots showed dynamic responses of tropical plant to cold stress

inferredcites →https://doi.org/10.1186/1471-2164-15-634openalex-snapshot

Endogenous small-noncoding RNAs and their roles in chilling response and stress acclimation in Cassava

inferredcites →https://doi.org/10.1186/1471-2229-7-66openalex-snapshot

Sequencing analysis of 20,000 full-length cDNA clones from cassava reveals lineage specific expansions in gene families related to stress response

inferredcites →https://doi.org/10.1186/s12864-016-2845-5openalex-snapshot

Exposure to various abscission-promoting treatments suggests substantial ERF subfamily transcription factors involvement in the regulation of cassava leaf abscission

inferredcites →https://doi.org/10.1186/s12870-014-0207-5openalex-snapshot

Chilling acclimation provides immunity to stress by altering regulatory networks and inducing genes with protective functions in Cassava

inferredcites →https://doi.org/10.1242/dev.01725openalex-snapshot

ROXY1 , a member of the plant glutaredoxin family, is required for petal development in Arabidopsis thaliana

inferredcites →https://doi.org/10.1371/journal.pone.0113718openalex-snapshot

Transcriptome Analysis Reveals Genes Commonly Induced by Botrytis cinerea Infection, Cold, Drought and Oxidative Stresses in Arabidopsis

inferredcites →https://doi.org/10.1371/journal.pone.0136993openalex-snapshot

Genome-Wide Identification and Expression Analysis of the NAC Transcription Factor Family in Cassava

inferredcites →https://doi.org/10.1515/hsz-2014-0300openalex-snapshot

Plant-specific CC-type glutaredoxins: functions in developmental processes and stress responses

inferredcites →https://doi.org/10.3389/fphys.2013.00093openalex-snapshot

Phenotypic approaches to drought in cassava: review

inferredcites →https://doi.org/10.3389/fpls.2015.00914openalex-snapshot

Genome-wide gene phylogeny of CIPK family in cassava and expression analysis of partial drought-induced genes

inferredcites →https://doi.org/10.3389/fpls.2015.00934openalex-snapshot

Overexpression of the CC-type glutaredoxin, OsGRX6 affects hormone and nitrogen status in rice plants

inferredcites →https://doi.org/10.4161/psb.24525openalex-snapshot

Coupled expression of Cu/Zn-superoxide dismutase and catalase in cassava improves tolerance against cold and drought stresses

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/s44340-024-00006-7openalex-snapshot

A review of drought-stress responsive genes and their applications for drought stress tolerance in cassava (Manihot esculenta Crantz)

inferred← citeshttps://doi.org/10.1111/nph.16346openalex-snapshot

The chaperone MeHSP90 recruits MeWRKY20 and MeCatalase1 to regulate drought stress resistance in cassava

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