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Characterization of the maize lipoxygenase gene family in relation to aflatoxin accumulation resistance

https://doi.org/10.1371/journal.pone.0181265

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What this work says

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

inferredcites →https://doi.org/10.1007/978-94-007-4264-2openalex-snapshot

Biocommunication of Fungi

inferredcites →https://doi.org/10.1007/978-94-007-4264-2_16openalex-snapshot

Lipid-Mediated Signaling Between Fungi and Plants

inferredcites →https://doi.org/10.1007/s11032-010-9446-9openalex-snapshot

Identification of novel QTL contributing resistance to aflatoxin accumulation in maize

inferredcites →https://doi.org/10.1007/s11032-012-9821-9openalex-snapshot

Confirming quantitative trait loci for aflatoxin resistance from Mp313E in different genetic backgrounds

inferredcites →https://doi.org/10.1016/j.fgb.2010.05.005openalex-snapshot

The lipid language of plant–fungal interactions

inferredcites →https://doi.org/10.1016/j.jplph.2015.09.003openalex-snapshot

Resistance to Fusarium verticillioides and fumonisin accumulation in maize inbred lines involves an earlier and enhanced expression of lipoxygenase (LOX) genes

inferredcites →https://doi.org/10.1016/j.pbi.2006.03.002openalex-snapshot

Green leaf volatiles: hydroperoxide lyase pathway of oxylipin metabolism

inferredcites →https://doi.org/10.1016/s0015-6264(70)80458-8openalex-snapshot

Aflatoxin. Scientific Background, Control and Implications

inferredcites →https://doi.org/10.1023/b:plan.0000004331.94803.b0openalex-snapshot

Dual positional specificity and expression of non-traditional lipoxygenase induced by wounding and methyl jasmonate in maize seedlings

inferredcites →https://doi.org/10.1038/nchembio.169openalex-snapshot

Chemical complexity of volatiles from plants induced by multiple attack

inferredcites →https://doi.org/10.1038/ng.2313openalex-snapshot

Maize HapMap2 identifies extant variation from a genome in flux

inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00324.xopenalex-snapshot

C6‐volatiles derived from the lipoxygenase pathway induce a subset of defense‐related genes

inferredcites →https://doi.org/10.1046/j.1439-0523.1999.118001001.xopenalex-snapshot

Aflatoxins in maize: The problem and genetic solutions

inferredcites →https://doi.org/10.1080/15569540802420584openalex-snapshot

Host-derived lipids and oxylipins are crucial signals in modulating mycotoxin production by fungi

inferredcites →https://doi.org/10.1093/bioinformatics/btm308openalex-snapshot

TASSEL: software for association mapping of complex traits in diverse samples

inferredcites →https://doi.org/10.1093/bioinformatics/btp120openalex-snapshot

TopHat: discovering splice junctions with RNA-Seq

inferredcites →https://doi.org/10.1093/bioinformatics/btu638openalex-snapshot

HTSeq—a Python framework to work with high-throughput sequencing data

inferredcites →https://doi.org/10.1093/jxb/erl137openalex-snapshot

Duplicate maize 13-lipoxygenase genes are differentially regulated by circadian rhythm, cold stress, wounding, pathogen infection, and hormonal treatments

inferredcites →https://doi.org/10.1093/molbev/msp077openalex-snapshot

FastTree: Computing Large Minimum Evolution Trees with Profiles instead of a Distance Matrix

inferredcites →https://doi.org/10.1093/nar/30.1.276openalex-snapshot

The Pfam Protein Families Database

inferredcites →https://doi.org/10.1093/nar/gkaa913openalex-snapshot

Pfam: The protein families database in 2021

inferredcites →https://doi.org/10.1093/nar/gkg033openalex-snapshot

Database resources of the National Center for Biotechnology

inferredcites →https://doi.org/10.1093/nar/gkh073openalex-snapshot

Database resources of the National Center for Biotechnology Information: update

inferredcites →https://doi.org/10.1093/nar/gkj154openalex-snapshot

Gramene: a bird's eye view of cereal genomes

inferredcites →https://doi.org/10.1093/nar/gks1109openalex-snapshot

PIECE: a database for plant gene structure comparison and evolution

inferredcites →https://doi.org/10.1093/nar/gks1189openalex-snapshot

Database resources of the National Center for Biotechnology Information

inferredcites →https://doi.org/10.1093/nar/gkt1140openalex-snapshot

Activities at the Universal Protein Resource (UniProt)

inferredcites →https://doi.org/10.1093/nar/gkt1223openalex-snapshot

Pfam: the protein families database

inferredcites →https://doi.org/10.1093/nar/gkv1007openalex-snapshot

MaizeGDB update: new tools, data and interface for the maize model organism database

inferredcites →https://doi.org/10.1094/mpmi-06-13-0184-ropenalex-snapshot

The Novel Monocot-Specific 9-Lipoxygenase ZmLOX12 Is Required to Mount an Effective Jasmonate-Mediated Defense Against Fusarium verticillioides in Maize

inferredcites →https://doi.org/10.1094/mpmi-20-8-0922openalex-snapshot

Disruption of a Maize 9-Lipoxygenase Results in Increased Resistance to Fungal Pathogens and Reduced Levels of Contamination with Mycotoxin Fumonisin

inferredcites →https://doi.org/10.1094/mpmi-21-1-0098openalex-snapshot

Maize 9-Lipoxygenase ZmLOX3 Controls Development, Root-Specific Expression of Defense Genes, and Resistance to Root-Knot Nematodes

inferredcites →https://doi.org/10.1094/phyto-74-1284openalex-snapshot

Preharvest Infection of Corn Silks and Kernels byAspergillus flavus

inferredcites →https://doi.org/10.1105/tpc.111.094151openalex-snapshot

Disruption of OPR7 and OPR8 Reveals the Versatile Functions of Jasmonic Acid in Maize Development and Defense

inferredcites →https://doi.org/10.1111/j.1439-0434.2007.01301.xopenalex-snapshot

Increased Resistance of a Maize Mutant Lacking the 9‐Lipoxygenase Gene, ZmLOX3, to Root Rot Caused by Exserohilum pedicellatum

inferredcites →https://doi.org/10.1111/tpj.12101openalex-snapshot

The maize lipoxygenase, Zm LOX 10 , mediates green leaf volatile, jasmonate and herbivore‐induced plant volatile production for defense against insect attack

inferredcites →https://doi.org/10.1126/science.1164645openalex-snapshot

tasselseed1 Is a Lipoxygenase Affecting Jasmonic Acid Signaling in Sex Determination of Maize

inferredcites →https://doi.org/10.1146/annurev.arplant.48.1.355openalex-snapshot

BIOSYNTHESIS AND ACTION OF JASMONATES IN PLANTS

inferredcites →https://doi.org/10.1146/annurev.arplant.53.100301.135248openalex-snapshot

T HE L IPOXYGENASE P ATHWAY

inferredcites →https://doi.org/10.1155/2008/496957openalex-snapshot

MaizeGDB: The Maize Model Organism Database for Basic, Translational, and Applied Research

inferredcites →https://doi.org/10.1155/2014/352831openalex-snapshot

Aflatoxin Resistance in Maize: What Have We Learned Lately?

inferredcites →https://doi.org/10.1186/1471-2164-16-1openalex-snapshot

Uncovering the novel characteristics of Asian honey bee, Apis cerana, by whole genome sequencing

inferredcites →https://doi.org/10.1186/1471-2164-16-s7-s12openalex-snapshot

Comprehensive genome-wide transcription factor analysis reveals that a combination of high affinity and low affinity DNA binding is needed for human gene regulation

inferredcites →https://doi.org/10.1186/s12864-015-1874-9openalex-snapshot

Using genome-wide associations to identify metabolic pathways involved in maize aflatoxin accumulation resistance

inferredcites →https://doi.org/10.1371/journal.pone.0053973openalex-snapshot

Characterization of Genetic Diversity and Linkage Disequilibrium of ZmLOX4 and ZmLOX5 Loci in Maize

inferredcites →https://doi.org/10.2135/cropsci2005.0171aopenalex-snapshot

Quantitative Trait Loci Contributing Resistance to Aflatoxin Accumulation in the Maize Inbred Mp313E

inferredcites →https://doi.org/10.2135/cropsci2008.12.0696openalex-snapshot

Identification and Mapping of New Sources of Resistance to Aflatoxin Accumulation in Maize

inferredcites →https://doi.org/10.2135/cropsci2012.10.0616openalex-snapshot

Phenotypic and Genetic Characterization of a Maize Association Mapping Panel Developed for the Identification of New Sources of Resistance to Aspergillus flavus and Aflatoxin Accumulation

inferredcites →https://doi.org/10.2135/cropsci2014.06.0424openalex-snapshot

Genome‐Wide Association Mapping of Aspergillus flavus and Aflatoxin Accumulation Resistance in Maize

inferredcites →https://doi.org/10.3835/plantgenome2012.09.0025openalex-snapshot

Maize Metabolic Network Construction and Transcriptome Analysis

inferredcites →https://doi.org/10.3835/plantgenome2015.04.0025openalex-snapshot

An Expanded Maize Gene Expression Atlas based on RNA Sequencing and its Use to Explore Root Development

inferredcites →https://doi.org/10.3920/wmj2014.1751openalex-snapshot

Identifying and developing maize germplasm with resistance to accumulation of aflatoxins

What points at this work

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

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Relative contribution of LOX10, green leaf volatiles and JA to wound-induced local and systemic oxylipin and hormone signature in Zea mays (maize)

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inferred← citeshttps://doi.org/10.1002/csc2.20629openalex-snapshot

Association mapping and pathway analysis of ear rot disease caused by Aspergillus flavus in a panel of tropical maize germplasm

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inferred← citeshttps://doi.org/10.1007/s00425-023-04114-2openalex-snapshot

Genome-wide identification and characterization of lipoxygenase genes related to the English grain aphid infestation response in wheat

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An overview of the transcriptional responses of two tolerant and susceptible sugarcane cultivars to borer (Diatraea saccharalis) infestation

inferred← citeshttps://doi.org/10.1007/s11033-023-08820-8openalex-snapshot

Low expression of lipoxygenase 3 (LOX3) enhances the retention of kernel tocopherols in maize during storage

inferred← citeshttps://doi.org/10.1007/s11103-020-01107-7openalex-snapshot

Genome-wide identification and classification of Lipoxygenase gene family and their roles in sorghum-aphid interaction

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ZmILI1 confers salt stress tolerance by regulating genes of phytohormone response in maize

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Lipoxygenases (LOXs): Will turning off this genetic switch help safeguard the flavor and nutritional quality of stored lipid-rich staple foods?

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Evolution and functional diversity of lipoxygenase (LOX) genes in allotetraploid rapeseed (Brassica napus L.)

inferred← citeshttps://doi.org/10.1016/j.micres.2019.126406openalex-snapshot

Selected isolates of Trichoderma gamsii induce different pathways of systemic resistance in maize upon Fusarium verticillioides challenge

inferred← citeshttps://doi.org/10.1016/j.molp.2023.07.003openalex-snapshot

9,10-KODA, an α-ketol produced by the tonoplast-localized 9-lipoxygenase ZmLOX5, plays a signaling role in maize defense against insect herbivory

inferred← citeshttps://doi.org/10.1016/j.pep.2026.106937openalex-snapshot

Extraction, purification and characterization of lipoxygenase from foxtail millet (Setaria italica)

inferred← citeshttps://doi.org/10.1016/j.plgene.2025.100557openalex-snapshot

Lipoxygenases: The gatekeepers in plant resilience against biotic stress

inferred← citeshttps://doi.org/10.1021/acs.jafc.4c01258openalex-snapshot

Discovery and Molecular Characterization of a Novel 9S-Lipoxygenase from Enhygromyxa salina for Fatty Acid Biotransformations

inferred← citeshttps://doi.org/10.1080/13102818.2020.1738956openalex-snapshot

Genome-wide identification and expression analysis of lipoxygenase genes in Tartary buckwheat

inferred← citeshttps://doi.org/10.1080/21645698.2025.2523069openalex-snapshot

CRISPR/Cas9-mediated editing of barley lipoxygenase genes promotes grain fatty acid accumulation and storability

inferred← citeshttps://doi.org/10.1088/1755-1315/432/1/012007openalex-snapshot

Plant defense-related gene expression analysis of canker-infected lime seedling

inferred← citeshttps://doi.org/10.1093/jxb/erab264openalex-snapshot

Reduced expression of lipoxygenase genes improves flour processing quality in soft wheat

inferred← citeshttps://doi.org/10.1093/jxb/erac522openalex-snapshot

Overexpression of maizeZmLOX6inArabidopsis thalianaenhances damage-induced pentyl leaf volatile emissions that affect plant growth and interaction with aphids

inferred← citeshttps://doi.org/10.1093/jxb/erad113openalex-snapshot

Combining quantitative trait locus mapping with multiomics profiling reveals genetic control of corn leaf aphid (Rhopalosiphum maidis) resistance in maize

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Maize Kernel Development Stage the Primary Factor in Differential Gene Expression in Response to Two Methods of Field Inoculation with Aspergillus flavus

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Combination of transcriptomic, proteomic, and degradomic profiling reveals common and distinct patterns of pathogen‐induced cell death in maize

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Disruption of allene oxide cyclase in maize reveals the necessity of enzymatically produced 12‐ OPDA for the induction of jasmonic acid during herbivory

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Transcriptomic and volatile signatures associated with maize defense against corn leaf aphid

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Additional file 7 of Transcriptomic and volatile signatures associated with maize defense against corn leaf aphid

inferred← citeshttps://doi.org/10.6084/m9.figshare.14594409openalex-snapshot

Additional file 10 of Comparative transcriptome profiling and co-expression network analysis uncover the key genes associated withearly-stage resistance to Aspergillus flavus in maize

inferred← citeshttps://doi.org/10.6084/m9.figshare.14594415openalex-snapshot

Additional file 11 of Comparative transcriptome profiling and co-expression network analysis uncover the key genes associated withearly-stage resistance to Aspergillus flavus in maize

inferred← citeshttps://doi.org/10.6084/m9.figshare.14594418openalex-snapshot

Additional file 1 of Comparative transcriptome profiling and co-expression network analysis uncover the key genes associated withearly-stage resistance to Aspergillus flavus in maize

inferred← citeshttps://doi.org/10.6084/m9.figshare.14594421openalex-snapshot

Additional file 2 of Comparative transcriptome profiling and co-expression network analysis uncover the key genes associated withearly-stage resistance to Aspergillus flavus in maize

inferred← citeshttps://doi.org/10.6084/m9.figshare.14594424openalex-snapshot

Additional file 3 of Comparative transcriptome profiling and co-expression network analysis uncover the key genes associated withearly-stage resistance to Aspergillus flavus in maize

inferred← citeshttps://doi.org/10.6084/m9.figshare.14594427openalex-snapshot

Additional file 4 of Comparative transcriptome profiling and co-expression network analysis uncover the key genes associated withearly-stage resistance to Aspergillus flavus in maize

inferred← citeshttps://doi.org/10.6084/m9.figshare.14594430openalex-snapshot

Additional file 5 of Comparative transcriptome profiling and co-expression network analysis uncover the key genes associated withearly-stage resistance to Aspergillus flavus in maize

inferred← citeshttps://doi.org/10.6084/m9.figshare.14594433openalex-snapshot

Additional file 6 of Comparative transcriptome profiling and co-expression network analysis uncover the key genes associated withearly-stage resistance to Aspergillus flavus in maize

inferred← citeshttps://doi.org/10.6084/m9.figshare.14594436openalex-snapshot

Additional file 7 of Comparative transcriptome profiling and co-expression network analysis uncover the key genes associated withearly-stage resistance to Aspergillus flavus in maize

inferred← citeshttps://doi.org/10.6084/m9.figshare.14594439openalex-snapshot

Additional file 8 of Comparative transcriptome profiling and co-expression network analysis uncover the key genes associated withearly-stage resistance to Aspergillus flavus in maize

inferred← citeshttps://doi.org/10.6084/m9.figshare.14594442openalex-snapshot

Additional file 9 of Comparative transcriptome profiling and co-expression network analysis uncover the key genes associated withearly-stage resistance to Aspergillus flavus in maize

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