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Lipid transfer from plants to arbuscular mycorrhiza fungi

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What this work says

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

inferredcites →https://doi.org/10.1002/bms.1200200804openalex-snapshot

Mass isotopomer analysis: Theoretical and practical considerations

inferredcites →https://doi.org/10.1007/978-1-62703-401-2openalex-snapshot

Plant Lipid Signaling Protocols

inferredcites →https://doi.org/10.1007/978-1-62703-401-2_8openalex-snapshot

Analysis and Quantification of Plant Membrane Lipids by Thin-Layer Chromatography and Gas Chromatography

inferredcites →https://doi.org/10.1007/978-3-662-07334-6_4openalex-snapshot

At the Interface Between Mycorrhizal Fungi and Plants: the Structural Organization of Cell Wall, Plasma Membrane and Cytoskeleton

inferredcites →https://doi.org/10.1007/s004250000324openalex-snapshot

Arbuscules of vesicular-arbuscular mycorrhizal fungi inhabit an acidic compartment within plant roots

inferredcites →https://doi.org/10.1016/0003-2697(86)90132-6openalex-snapshot

Fatty acid composition of leaf lipids determined after combined digestion and fatty acid methyl ester formation from fresh tissue

inferredcites →https://doi.org/10.1016/j.chroma.2010.01.016openalex-snapshot

Identification of monoacylglycerol regio-isomers by gas chromatography–mass spectrometry

inferredcites →https://doi.org/10.1016/j.cub.2012.09.043openalex-snapshot

A Common Signaling Process that Promotes Mycorrhizal and Oomycete Colonization of Plants

inferredcites →https://doi.org/10.1016/j.cub.2012.09.044openalex-snapshot

A GRAS-Type Transcription Factor with a Specific Function in Mycorrhizal Signaling

inferredcites →https://doi.org/10.1016/j.cub.2016.01.069openalex-snapshot

A CCaMK-CYCLOPS-DELLA Complex Activates Transcription of RAM1 to Regulate Arbuscule Branching

inferredcites →https://doi.org/10.1016/j.molp.2016.02.003openalex-snapshot

Plant ABC Transporters Enable Many Unique Aspects of a Terrestrial Plant's Lifestyle

inferredcites →https://doi.org/10.1016/j.phytochem.2005.01.020openalex-snapshot

Lipid metabolism in arbuscular mycorrhizal roots of Medicago truncatula

inferredcites →https://doi.org/10.1016/s0003-9861(02)00017-6openalex-snapshot

Characterization of substrate specificity of plant FatA and FatB acyl-ACP thioesterases

inferredcites →https://doi.org/10.1016/s0038-0717(01)00151-1openalex-snapshot

Use of fatty acids for identification of AM fungi and estimation of the biomass of AM spores in soil

inferredcites →https://doi.org/10.1038/ismej.2015.91openalex-snapshot

Symbiosis with an endobacterium increases the fitness of a mycorrhizal fungus, raising its bioenergetic potential

inferredcites →https://doi.org/10.1038/nchembio.960openalex-snapshot

The identification of cutin synthase: formation of the plant polyester cutin

inferredcites →https://doi.org/10.1038/nmicrobiol.2016.33openalex-snapshot

Evidence for the sexual origin of heterokaryosis in arbuscular mycorrhizal fungi

inferredcites →https://doi.org/10.1038/nplants.2015.208openalex-snapshot

Genes conserved for arbuscular mycorrhizal symbiosis identified through phylogenomics

inferredcites →https://doi.org/10.1073/pnas.0608136104openalex-snapshot

A Medicago truncatula phosphate transporter indispensable for the arbuscular mycorrhizal symbiosis

inferredcites →https://doi.org/10.1073/pnas.0806858105openalex-snapshot

CYCLOPS, a mediator of symbiotic intracellular accommodation

inferredcites →https://doi.org/10.1073/pnas.0914149107openalex-snapshot

A distinct type of glycerol-3-phosphate acyltransferase with sn -2 preference and phosphatase activity producing 2-monoacylglycerol

inferredcites →https://doi.org/10.1073/pnas.1515426112openalex-snapshot

Algal ancestor of land plants was preadapted for symbiosis

inferredcites →https://doi.org/10.1073/pnas.93.11.5659openalex-snapshot

Congruence of fatty acid methyl ester profiles and morphological characters of arbuscular mycorrhizal fungi in Gigasporaceae.

inferredcites →https://doi.org/10.1074/jbc.m110.210880openalex-snapshot

Sequences in the Nonconsensus Nucleotide-binding Domain of ABCG5/ABCG8 Required for Sterol Transport

inferredcites →https://doi.org/10.1074/jbc.m205375200openalex-snapshot

Profiling Membrane Lipids in Plant Stress Responses

inferredcites →https://doi.org/10.1093/database/bau077openalex-snapshot

'Isotopo' a database application for facile analysis and management of mass isotopomer data

inferredcites →https://doi.org/10.1093/dnares/dsn008openalex-snapshot

Genome Structure of the Legume, Lotus japonicus

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/pcp/pcu024openalex-snapshot

Isolation and Phenotypic Characterization of Lotus japonicus Mutants Specifically Defective in Arbuscular Mycorrhizal Formation

inferredcites →https://doi.org/10.1104/pp.102.007765openalex-snapshot

Carbon Export from Arbuscular Mycorrhizal Roots Involves the Translocation of Carbohydrate as well as Lipid

inferredcites →https://doi.org/10.1104/pp.102.017384openalex-snapshot

A TILLING Reverse Genetics Tool and a Web-Accessible Collection of Mutants of the Legume Lotus japonicus

inferredcites →https://doi.org/10.1104/pp.107.099432openalex-snapshot

Monoacylglycerols Are Components of Root Waxes and Can Be Produced in the Aerial Cuticle by Ectopic Expression of a Suberin-Associated Acyltransferase

inferredcites →https://doi.org/10.1104/pp.107.1.7openalex-snapshot

The Shikimate Pathway as an Entry to Aromatic Secondary Metabolism

inferredcites →https://doi.org/10.1104/pp.108.124867openalex-snapshot

Finding and Comparing Syntenic Regions among Arabidopsis and the Outgroups Papaya, Poplar, and Grape: CoGe with Rosids

inferredcites →https://doi.org/10.1104/pp.109.142190openalex-snapshot

TILLING in Lotus japonicus Identified Large Allelic Series for Symbiosis Genes and Revealed a Bias in Functionally Defective Ethyl Methanesulfonate Alleles toward Glycine Replacements

inferredcites →https://doi.org/10.1104/pp.112.201996openalex-snapshot

A Land-Plant-Specific Glycerol-3-Phosphate Acyltransferase Family in Arabidopsis: Substrate Specificity, sn -2 Preference, and Evolution

inferredcites →https://doi.org/10.1104/pp.114.255430openalex-snapshot

Network of GRAS Transcription Factors Involved in the Control of Arbuscule Development inLotus japonicus

inferredcites →https://doi.org/10.1104/pp.120.2.587openalex-snapshot

Carbon Uptake and the Metabolism and Transport of Lipids in an Arbuscular Mycorrhiza1

inferredcites →https://doi.org/10.1104/pp.15.01155openalex-snapshot

Hyphal branching during arbuscule development requires RAM1

inferredcites →https://doi.org/10.1105/tpc.108.059014openalex-snapshot

Prepenetration Apparatus Assembly Precedes and Predicts the Colonization Patterns of Arbuscular Mycorrhizal Fungi within the Root Cortex of Both Medicago truncatula and Daucus carota

inferredcites →https://doi.org/10.1105/tpc.109.069807openalex-snapshot

NENA , a Lotus japonicus Homolog of Sec13 , Is Required for Rhizodermal Infection by Arbuscular Mycorrhiza Fungi and Rhizobia but Dispensable for Cortical Endosymbiotic Development

inferredcites →https://doi.org/10.1105/tpc.110.074955openalex-snapshot

Two Medicago truncatula Half-ABC Transporters Are Essential for Arbuscule Development in Arbuscular Mycorrhizal Symbiosis

inferredcites →https://doi.org/10.1105/tpc.110.075564openalex-snapshot

Arabidopsis β-Ketoacyl-[Acyl Carrier Protein] Synthase I Is Crucial for Fatty Acid Synthesis and Plays a Role in Chloroplast Division and Embryo Development

inferredcites →https://doi.org/10.1105/tpc.111.089813openalex-snapshot

A Versatile Monosaccharide Transporter That Operates in the Arbuscular Mycorrhizal Fungus Glomus sp Is Crucial for the Symbiotic Relationship with Plants

inferredcites →https://doi.org/10.1105/tpc.111.091827openalex-snapshot

Nuclear-Localized and Deregulated Calcium- and Calmodulin-Dependent Protein Kinase Activates Rhizobial and Mycorrhizal Responses in Lotus japonicus

inferredcites →https://doi.org/10.1105/tpc.112.095588openalex-snapshot

Fatty Acid Phytyl Ester Synthesis in Chloroplasts of Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.7.3.359openalex-snapshot

Palmitoyl-acyl carrier protein (ACP) thioesterase and the evolutionary origin of plant acyl-ACP thioesterases.

inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03824.xopenalex-snapshot

Apoplastic plant subtilases support arbuscular mycorrhiza development in Lotus japonicus

inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04810.xopenalex-snapshot

Arbuscule‐containing and non‐colonized cortical cells of mycorrhizal roots undergo extensive and specific reprogramming during arbuscular mycorrhizal development

inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04842.xopenalex-snapshot

The half‐size ABC transporters STR1 and STR2 are indispensable for mycorrhizal arbuscule formation in rice

inferredcites →https://doi.org/10.1111/j.1469-8137.1988.tb03698.xopenalex-snapshot

Early events of vesicular–arbuscular mycorrhiza formation on Ri T‐DNA transformed roots

inferredcites →https://doi.org/10.1111/j.1469-8137.1990.tb00476.xopenalex-snapshot

A new method which gives an objective measure of colonization of roots by vesicular—arbuscular mycorrhizal fungi

inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03608.xopenalex-snapshot

The Arabidopsis ABCG13 transporter is required for flower cuticle secretion and patterning of the petal epidermis

inferredcites →https://doi.org/10.1111/nph.13608openalex-snapshot

The ABCG transporter PEC1/ABCG32 is required for the formation of the developing leaf cuticle in Arabidopsis

inferredcites →https://doi.org/10.1111/nph.14403openalex-snapshot

Phosphorus acquisition efficiency in arbuscular mycorrhizal maize is correlated with the abundance of root‐external hyphae and the accumulation of transcripts encoding PHT1 phosphate transporters

inferredcites →https://doi.org/10.1111/nph.14533openalex-snapshot

Arbuscular mycorrhiza‐specific enzymes FatM and RAM 2 fine‐tune lipid biosynthesis to promote development of arbuscular mycorrhiza

inferredcites →https://doi.org/10.1111/tpj.12045openalex-snapshot

An AM ‐induced, MYB ‐family gene of Lotus japonicus (Lj MAMI ) affects root growth in an AM ‐independent manner

inferredcites →https://doi.org/10.1111/tpj.12220openalex-snapshot

Two L otus japonicus symbiosis mutants impaired at distinct steps of arbuscule development

inferredcites →https://doi.org/10.1111/tpj.12241openalex-snapshot

The role of lipid metabolism in the acquisition of desiccation tolerance in C raterostigma plantagineum: a comparative approach

inferredcites →https://doi.org/10.1111/tpj.12566openalex-snapshot

Fatty acid synthesis and lipid metabolism in the obligate biotrophic fungus R hizophagus irregularis during mycorrhization of L otus japonicus

inferredcites →https://doi.org/10.1111/tpj.12706openalex-snapshot

A set of fluorescent protein‐based markers expressed from constitutive and arbuscular mycorrhiza‐inducible promoters to label organelles, membranes and cytoskeletal elements in Medicago truncatula

inferredcites →https://doi.org/10.1126/science.1102331openalex-snapshot

Plant Cuticular Lipid Export Requires an ABC Transporter

inferredcites →https://doi.org/10.1128/aem.61.1.58-64.1995openalex-snapshot

Fatty Acid methyl ester profiles for characterization of glomalean fungi and their endomycorrhizae

inferredcites →https://doi.org/10.1128/aem.64.12.5004-5007.1998openalex-snapshot

Ink and Vinegar, a Simple Staining Technique for Arbuscular-Mycorrhizal Fungi

inferredcites →https://doi.org/10.1128/aem.69.11.6762-6767.2003openalex-snapshot

Fungal Lipid Accumulation and Development of Mycelial Structures by Two Arbuscular Mycorrhizal Fungi

inferredcites →https://doi.org/10.1128/aem.71.9.5341-5347.2005openalex-snapshot

Dependence of Arbuscular-Mycorrhizal Fungi on Their Plant Host for Palmitic Acid Synthesis

inferredcites →https://doi.org/10.1128/ec.00002-11openalex-snapshot

Evidence for Host Cells as the Major Contributor of Lipids in the Intravacuolar Network of Toxoplasma-Infected Cells

inferredcites →https://doi.org/10.1152/ajpendo.90899.2008openalex-snapshot

Intestinal lipid absorption

inferredcites →https://doi.org/10.1172/jci200216548openalex-snapshot

Biliary cholesterol secretion by the twinned sterol half-transporters ABCG5 and ABCG8

inferredcites →https://doi.org/10.1177/002215549904700910openalex-snapshot

Alexa Dyes, a Series of New Fluorescent Dyes that Yield Exceptionally Bright, Photostable Conjugates

inferredcites →https://doi.org/10.1186/s12870-014-0333-0openalex-snapshot

A novel bioinformatics pipeline to discover genes related to arbuscular mycorrhizal symbiosis based on their evolutionary conservation pattern among higher plants

inferredcites →https://doi.org/10.1194/jlr.d013987openalex-snapshot

Quantification of sterol lipids in plants by quadrupole time-of-flight mass spectrometry

inferredcites →https://doi.org/10.1199/tab.0133openalex-snapshot

Acyl-Lipid Metabolism

inferredcites →https://doi.org/10.1371/journal.pgen.1004487openalex-snapshot

Comparative Phylogenomics Uncovers the Impact of Symbiotic Associations on Host Genome Evolution

inferredcites →https://doi.org/10.1371/journal.pone.0088218openalex-snapshot

A Modular Plasmid Assembly Kit for Multigene Expression, Gene Silencing and Silencing Rescue in Plants

inferredcites →https://doi.org/10.1371/journal.ppat.1002198openalex-snapshot

Chlamydia trachomatis Co-opts GBF1 and CERT to Acquire Host Sphingomyelin for Distinct Roles during Intracellular Development

inferredcites →https://doi.org/10.1385/1-59259-192-2:365openalex-snapshot

Primer3 on the WWW for General Users and for Biologist Programmers

inferredcites →https://doi.org/10.3389/fmicb.2016.00233openalex-snapshot

A Survey of the Gene Repertoire of Gigaspora rosea Unravels Conserved Features among Glomeromycota for Obligate Biotrophy

inferredcites →https://doi.org/10.4161/psb.19650openalex-snapshot

Cell type-specific protein and transcription profiles implicate periarbuscular membrane synthesis as an important carbon sink in the mycorrhizal symbiosis

inferredcites →https://doi.org/10.4161/psb.26049openalex-snapshot

RAM1andRAM2function and expression during Arbuscular Mycorrhizal Symbiosis andAphanomyces euteichescolonization

inferredcites →https://doi.org/10.7554/elife.02964openalex-snapshot

Insect endosymbiont proliferation is limited by lipid availability

What points at this work

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

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Symrk Significantly Affected Am Fungal Symbiosis and Plant Growth in Maize

inferred← citeshttps://doi.org/10.1038/s41598-021-87886-5openalex-snapshot

Metabolomics and transcriptomics to decipher molecular mechanisms underlying ectomycorrhizal root colonization of an oak tree

inferred← citeshttps://doi.org/10.1038/s41598-022-23502-4openalex-snapshot

Label-free third harmonic generation imaging and quantification of lipid droplets in live filamentous fungi

inferred← citeshttps://doi.org/10.1093/pcp/pcz122openalex-snapshot

Structure-Specific Regulation of Nutrient Transport and Metabolism in Arbuscular Mycorrhizal Fungi

inferred← citeshttps://doi.org/10.1111/pce.15612openalex-snapshot

Metabolic Shifts and Nutrient Transfer Patterns in Orchid Seeds During Symbiotic Germination

inferred← citeshttps://doi.org/10.1111/prd.12360openalex-snapshot

Interactions of host‐associated multispecies bacterial communities

inferred← citeshttps://doi.org/10.1186/s40538-019-0150-7openalex-snapshot

To trade in the field: the molecular determinants of arbuscular mycorrhiza nutrient exchange

inferred← citeshttps://doi.org/10.18174/547713openalex-snapshot

Partner control in arbuscular mycorrhizal symbiosis

inferred← citeshttps://doi.org/10.21931/rb/2019.04.04.6openalex-snapshot

The intensity of symbiotic relationships between arbuscular mycorrhizae and differentiated tree species regarding their age group and plant family in semi-arid Andine dynamical agroforestry system

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Descripción morfológica y caracterización molecular de los hongos asociados a la raíz de Masdevallia coccinea Linden ex Lindl.

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