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TabHLH1, a bHLH-type transcription factor gene in wheat, improves plant tolerance to Pi and N deprivation via regulation of nutrient transporter gene transcription and ROS homeostasis

https://doi.org/10.1016/j.plaphy.2016.03.023
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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/s00239-002-2449-3openalex-snapshot
Phylogenetic Analysis of Plant Basic Helix-Loop-Helix Proteins
inferredcites →https://doi.org/10.1007/s00299-011-1068-0openalex-snapshot
Plant tolerance to drought and salinity: stress regulating transcription factors and their functional significance in the cellular transcriptional network
inferredcites →https://doi.org/10.1007/s00425-004-1266-xopenalex-snapshot
Disruption of the nitrate transporter genes AtNRT2.1 and AtNRT2.2 restricts growth at low external nitrate concentration
inferredcites →https://doi.org/10.1007/s00425-005-0015-0openalex-snapshot
Cereal phosphate transporters associated with the mycorrhizal pathway of phosphate uptake into roots
inferredcites →https://doi.org/10.1007/s00425-012-1836-2openalex-snapshot
Function of wheat phosphate transporter gene TaPHT2;1 in Pi translocation and plant growth regulation under replete and limited Pi supply conditions
inferredcites →https://doi.org/10.1007/s11103-008-9380-yopenalex-snapshot
Plant hormones and nutrient signaling
inferredcites →https://doi.org/10.1007/s11703-011-1069-3openalex-snapshot
Effects of chromosome substitution on the utilization efficiency of nitrogen, phosphorus, and potassium in wheat
inferredcites →https://doi.org/10.1016/b978-0-12-473542-2.x5000-7openalex-snapshot
Mineral Nutrition of Higher Plants
inferredcites →https://doi.org/10.1016/j.gene.2006.10.009openalex-snapshot
Deciphering the regulatory mechanisms of abiotic stress tolerance in plants by genomic approaches
inferredcites →https://doi.org/10.1016/j.gene.2008.10.016openalex-snapshot
Identification of ICE2, a gene involved in cold acclimation which determines freezing tolerance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.plantsci.2011.11.010openalex-snapshot
A full-length R-like basic-helix-loop-helix transcription factor is required for anthocyanin upregulation whereas the N-terminal region regulates epidermal hair formation
inferredcites →https://doi.org/10.1016/j.plaphy.2010.08.016openalex-snapshot
Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants
inferredcites →https://doi.org/10.1016/s0014-5793(01)02096-8openalex-snapshot
An Arabidopsis T‐DNA mutant affected in Nrt2 genes is impaired in nitrate uptake
inferredcites →https://doi.org/10.1016/s0092-8674(00)81636-0openalex-snapshot
PIF3, a Phytochrome-Interacting Factor Necessary for Normal Photoinduced Signal Transduction, Is a Novel Basic Helix-Loop-Helix Protein
inferredcites →https://doi.org/10.1016/s1671-2927(12)60780-9openalex-snapshot
Molecular Characterization and Expression Analysis of TaZFP15, a C2H2-Type Zinc Finger Transcription Factor Gene in Wheat (Triticum aestivum L.)
inferredcites →https://doi.org/10.1034/j.1399-3054.2001.1120204.xopenalex-snapshot
Role of the Arabidopsis CBF transcriptional activators in cold acclimation
inferredcites →https://doi.org/10.1034/j.1399-3054.2001.1120405.xopenalex-snapshot
Response of the cultivated tomato and its wild salt‐tolerant relative Lycopersiconpennellii to salt‐dependent oxidative stress: The root antioxidative system
inferredcites →https://doi.org/10.1038/cr.2008.26openalex-snapshot
FIT interacts with AtbHLH38 and AtbHLH39 in regulating iron uptake gene expression for iron homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1038/nature11909openalex-snapshot
Using membrane transporters to improve crops for sustainable food production
inferredcites →https://doi.org/10.1071/fp12242openalex-snapshot
TaPht1;4, a high-affinity phosphate transporter gene in wheat (Triticum aestivum), plays an important role in plant phosphate acquisition under phosphorus deprivation
inferredcites →https://doi.org/10.1073/pnas.0407107101openalex-snapshot
The phytochrome-interacting transcription factor, PIF3, acts early, selectively, and positively in light-induced chloroplast development
inferredcites →https://doi.org/10.1073/pnas.1118876109openalex-snapshot
FLOWERING BHLH transcriptional activators control expression of the photoperiodic flowering regulator CONSTANS in Arabidopsis
inferredcites →https://doi.org/10.1080/10715769900301561openalex-snapshot
Purification of Catalase from Pea Leaf Peroxisomes: Identification of Five Different Isoforms
inferredcites →https://doi.org/10.1093/emboj/21.10.2441openalex-snapshot
PIF4, a phytochrome‐interacting bHLH factor, functions as a negative regulator of phytochrome B signaling in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/erh103openalex-snapshot
Characterization of promoter expression patterns derived from the Pht1 phosphate transporter genes of barley (Hordeum vulgare L.)
inferredcites →https://doi.org/10.1093/jxb/erq409openalex-snapshot
From the soil to the seeds: the long journey of nitrate in plants
inferredcites →https://doi.org/10.1093/jxb/err216openalex-snapshot
A bHLH transcription factor, DvIVS, is involved in regulation of anthocyanin synthesis in dahlia (Dahlia variabilis)
inferredcites →https://doi.org/10.1093/jxb/err229openalex-snapshot
Cloning and molecular characterization of a mitogen-activated protein kinase gene from Poncirus trifoliata whose ectopic expression confers dehydration/drought tolerance in transgenic tobacco
inferredcites →https://doi.org/10.1093/molbev/msp288openalex-snapshot
Origin and Diversification of Basic-Helix-Loop-Helix Proteins in Plants
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a078903openalex-snapshot
Plant Transcription Factors
inferredcites →https://doi.org/10.1093/pcp/pcq095openalex-snapshot
Recent Progress in Plant Nutrition Research: Cross-Talk Between Nutrients, Plant Physiology and Soil Microorganisms
inferredcites →https://doi.org/10.1093/treephys/tpq030openalex-snapshot
Spermine pretreatment confers dehydration tolerance of citrus in vitro plants via modulation of antioxidative capacity and stomatal response
inferredcites →https://doi.org/10.1101/gad.1077503openalex-snapshot
ICE1: a regulator of cold-induced transcriptome and freezing tolerance in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.828000openalex-snapshot
Functional selectivity of recombinant mammalian SWI/SNF subunits
inferredcites →https://doi.org/10.1104/pp.104.045823openalex-snapshot
Promoter Analysis of the Barley Pht1;1 Phosphate Transporter Gene Identifies Regions Controlling Root Expression and Responsiveness to Phosphate Deprivation
inferredcites →https://doi.org/10.1104/pp.105.063115openalex-snapshot
OsPTF1, a Novel Transcription Factor Involved in Tolerance to Phosphate Starvation in Rice
inferredcites →https://doi.org/10.1104/pp.106.080580openalex-snapshot
Genome-Wide Analysis of Basic/Helix-Loop-Helix Transcription Factor Family in Rice and Arabidopsis
inferredcites →https://doi.org/10.1104/pp.106.091223openalex-snapshot
Dissection of the AtNRT2.1 : AtNRT2.2 Inducible High-Affinity Nitrate Transporter Gene Cluster
inferredcites →https://doi.org/10.1104/pp.108.129791openalex-snapshot
Transcriptional Regulatory Networks in Response to Abiotic Stresses in Arabidopsis and Grasses
inferredcites →https://doi.org/10.1104/pp.109.143867openalex-snapshot
Conservation of Lotus and Arabidopsis Basic Helix-Loop-Helix Proteins Reveals New Players in Root Hair Development
inferredcites →https://doi.org/10.1104/pp.111.190983openalex-snapshot
Co-Overexpression FIT with AtbHLH38 or AtbHLH39 in Arabidopsis-Enhanced Cadmium Tolerance via Increased Cadmium Sequestration in Roots and Improved Iron Homeostasis of Shoots
inferredcites →https://doi.org/10.1104/pp.112.210740openalex-snapshot
A Basic Helix-Loop-Helix Transcription Factor, PtrbHLH, of Poncirus trifoliata Confers Cold Tolerance and Modulates Peroxidase-Mediated Scavenging of Hydrogen Peroxide
inferredcites →https://doi.org/10.1105/tpc.006130openalex-snapshot
Arabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) Function as Transcriptional Activators in Abscisic Acid Signaling
inferredcites →https://doi.org/10.1105/tpc.013839openalex-snapshot
The Arabidopsis Basic/Helix-Loop-Helix Transcription Factor Family[W]
inferredcites →https://doi.org/10.1105/tpc.12.10.1863openalex-snapshot
The TT8 Gene Encodes a Basic Helix-Loop-Helix Domain Protein Required for Expression of DFR and BAN Genes in Arabidopsis Siliques
inferredcites →https://doi.org/10.1111/j.1365-3040.2009.02041.xopenalex-snapshot
Reactive oxygen species homeostasis and signalling during drought and salinity stresses
inferredcites →https://doi.org/10.1111/j.1365-3040.2012.02523.xopenalex-snapshot
The bHLH transcription factor MdbHLH3 promotes anthocyanin accumulation and fruit colouration in response to low temperature in apples
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04239.xopenalex-snapshot
Identification of a nitrate‐responsive cis ‐element in the Arabidopsis NIR1 promoter defines the presence of multiple cis ‐regulatory elements for nitrogen response
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04477.xopenalex-snapshot
OsbHLH148, a basic helix‐loop‐helix protein, interacts with OsJAZ proteins in a jasmonate signaling pathway leading to drought tolerance in rice
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03718.xopenalex-snapshot
MtbHLH1, a bHLH transcription factor involved in Medicago truncatula nodule vascular patterning and nodule to plant metabolic exchanges
inferredcites →https://doi.org/10.1146/annurev-arplant-042110-103849openalex-snapshot
Signaling Network in Sensing Phosphate Availability in Plants
inferredcites →https://doi.org/10.1146/annurev-arplant-042811-105522openalex-snapshot
Iron Uptake, Translocation, and Regulation in Higher Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.51.1.463openalex-snapshot
P LANT C ELLULAR AND M OLECULAR R ESPONSES TO H IGH S ALINITY
inferredcites →https://doi.org/10.1146/annurev.arplant.58.032806.103750openalex-snapshot
Nutrient Sensing and Signaling: NPKS
inferredcites →https://doi.org/10.1155/2015/603182openalex-snapshot
A Classification of Basic Helix-Loop-Helix Transcription Factors of Soybean
inferredcites →https://doi.org/10.1186/1471-2148-12-154openalex-snapshot
Accurate discrimination of bHLH domains in plants, animals, and fungi using biologically meaningful sites
inferredcites →https://doi.org/10.1186/1471-2229-10-230openalex-snapshot
Overexpression of PtrABF gene, a bZIP transcription factor isolated from Poncirus trifoliata, enhances dehydration and drought tolerance in tobacco via scavenging ROS and modulating expression of stress-responsive genes
inferredcites →https://doi.org/10.1186/1471-2229-12-22openalex-snapshot
The cold-induced basic helix-loop-helix transcription factor gene MdCIbHLH1encodes an ICE-like protein in apple
inferredcites →https://doi.org/10.1242/dev.00880openalex-snapshot
The bHLH genes GLABRA3 (GL3) and ENHANCER OF GLABRA3(EGL3) specify epidermal cell fate in the Arabidopsis root
inferredcites →https://doi.org/10.1371/journal.pone.0044843openalex-snapshot
Arabidopsis bHLH100 and bHLH101 Control Iron Homeostasis via a FIT-Independent Pathway
inferredcites →https://doi.org/10.1371/journal.pone.0137098openalex-snapshot
Overexpression of EcbHLH57 Transcription Factor from Eleusine coracana L. in Tobacco Confers Tolerance to Salt, Oxidative and Drought Stress
inferredcites →https://doi.org/10.3389/fpls.2011.00083openalex-snapshot
Phosphate import in plants: focus on the PHT1 transporters
inferredcites →https://doi.org/10.3969/j.issn.1000-5137.2017.05.018openalex-snapshot
Iron uptake, translocation, and regulation in higher plants

What points at this work

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

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inferred← citeshttps://doi.org/10.1093/jxb/erz307openalex-snapshot
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