Symbiosis genes for immunity and vice versa
Tóm tắt
Từ khóa
Tài liệu tham khảo
Badis, 2015, Transcriptome analysis highlights preformed defences and signalling pathways controlled by the prAe1 quantitative trait locus (QTL), conferring partial resistance to Aphanomyces euteiches in Medicago truncatula, Mol Plant Pathol, 16, 973, 10.1111/mpp.12253
Liu, 2017, Ethylene signaling is important for isoflavonoid-mediated resistance to Rhizoctonia solani in roots of Medicago truncatula, Mol Plant Microbe Interact, 30, 691, 10.1094/MPMI-03-17-0057-R
Ben, 2013, MtQRRS1, an R-locus required for Medicago truncatula quantitative resistance to Ralstonia solanacearum, New Phytol, 199, 758, 10.1111/nph.12299
Nishimura, 2010, Arabidopsis and the plant immune system, Plant J, 61, 1053, 10.1111/j.1365-313X.2010.04131.x
Rey, 2013, NFP, a LysM protein controlling Nod factor perception, also intervenes in Medicago truncatula resistance to pathogens, New Phytol, 198, 875, 10.1111/nph.12198
Rey, 2015, Medicago truncatula symbiosis mutants affected in the interaction with a biotrophic root pathogen, New Phytol, 206, 497, 10.1111/nph.13233
Ben, 2013, Natural diversity in the model legume Medicago truncatula allows identifying distinct genetic mechanisms conferring partial resistance to Verticillium wilt, J Exp Bot, 64, 317, 10.1093/jxb/ers337
Moreau, 2014, The symbiotic transcription factor MtEFD and cytokinins are positively acting in the Medicago truncatula and Ralstonia solanacearum pathogenic interaction, New Phytol, 201, 1343, 10.1111/nph.12636
Zhang, 2015, The receptor kinase CERK1 has dual functions in symbiosis and immunity signalling, Plant J, 81, 258, 10.1111/tpj.12723
Buendia, 2016, The LysM receptor-like kinase SlLYK 10 regulates the arbuscular mycorrhizal symbiosis in tomato, New Phytol, 210, 184, 10.1111/nph.13753
Tanaka, 2015, Effect of lipo-chitooligosaccharide on early growth of C4 grass seedlings, J Exp Bot, 66, 5727, 10.1093/jxb/erv260
Liang, 2013, Nonlegumes respond to rhizobial Nod factors by suppressing the innate immune response, Science, 341, 1384, 10.1126/science.1242736
Carotenuto, 2017, The rice LysM receptor-like kinase OsCERK1 is required for the perception of short-chain chitin oligomers in arbuscular mycorrhizal signaling, New Phytol, 214, 1440, 10.1111/nph.14539
Genre, 2013, Short-chain chitin oligomers from arbuscular mycorrhizal fungi trigger nuclear Ca2+ spiking in Medicago truncatula roots and their production is enhanced by strigolactone, New Phytol, 198, 190, 10.1111/nph.12146
Gourion, 2015, Rhizobium–legume symbioses: the crucial role of plant immunity, Trends Plant Sci, 20, 186, 10.1016/j.tplants.2014.11.008
Domonkos, 2017, NAD1 controls defense-like responses in Medicago truncatula symbiotic nitrogen fixing nodules following rhizobial colonization in a BacA-independent manner, Genes, 8, 387, 10.3390/genes8120387
Fuechtbauer, 2017, LYS12 LysM receptor decelerates Phytophthora palmivora disease progression in Lotus japonicus, Plant J, 93, 297, 10.1111/tpj.13785
Shinya, 2015, Chitin-mediated plant–fungal interactions: catching, hiding and handshaking, Curr Opin Plant Biol, 26, 64, 10.1016/j.pbi.2015.05.032
Cao, 2017, The role of plant innate immunity in the legume–rhizobium symbiosis, Annu Rev Plant Biol, 68, 535, 10.1146/annurev-arplant-042916-041030
Desaki, 2017, OsCERK1 plays a crucial role in the lipopolysaccharide-induced immune response of rice, New Phytol, 217, 1042, 10.1111/nph.14941
Miyata, 2014, The bifunctional plant receptor, OsCERK1, regulates both chitin-triggered immunity and arbuscular mycorrhizal symbiosis in rice, Plant Cell Physiol, 55, 1864, 10.1093/pcp/pcu129
Miyata, 2016, Evaluation of the role of the LysM receptor-like kinase, OsNFR5/OsRLK2 for AM symbiosis in rice, Plant Cell Physiol, 57, 2283, 10.1093/pcp/pcw144
Liu, 2012, Chitin-induced dimerization activates a plant immune receptor, Science, 336, 1160, 10.1126/science.1218867
Hayafune, 2014, Chitin-induced activation of immune signaling by the rice receptor CEBiP relies on a unique sandwich-type dimerization, Proc Natl Acad Sci U S A, 11, 404, 10.1073/pnas.1312099111
Le, 2014, LIK1, a CERK1-interacting kinase, regulates plant immune responses in Arabidopsis, PLoS One, 9, e102245, 10.1371/journal.pone.0102245
Shinya, 2017, Selective regulation of the chitin-induced defense response by the Arabidopsis receptor-like cytoplasmic kinase PBL27, Plant J, 79, 56, 10.1111/tpj.12535
Yamada, 2016, The Arabidopsis CERK1-associated kinase PBL27 connects chitin perception to MAPK activation, EMBO J, 35, 2468, 10.15252/embj.201694248
Espinoza, 2017, Chitin receptor CERK1 links salt stress and chitin-triggered innate immunity in Arabidopsis, Plant J, 89, 984, 10.1111/tpj.13437
Ben Amor, 2003, The NFP locus of Medicago truncatula controls an early step of Nod factor signal transduction upstream of a rapid calcium flux and root hair deformation, Plant J, 34, 495, 10.1046/j.1365-313X.2003.01743.x
Czaja, 2012, Transcriptional responses toward diffusible signals from symbiotic microbes reveal MtNFP- and MtDMI3-dependent reprogramming of host gene expression by arbuscular mycorrhizal fungal lipochitooligosaccharides, Plant Physiol, 159, 1671, 10.1104/pp.112.195990
Buendia, 2016, The LysM receptor-like kinase SlLYK10 regulates the arbuscular mycorrhizal symbiosis in tomato, New Phytol, 210, 184, 10.1111/nph.13753
Gough, 2013, Nod factor perception protein carries weight in biotic interactions, Trends Plant Sci, 18, 566, 10.1016/j.tplants.2013.06.001
Moling, 2014, Nod factor receptors form heteromeric complexes and are essential for intracellular infection in Medicago nodules, Plant Cell, 26, 4188, 10.1105/tpc.114.129502
Pietraszewska-Bogiel, 2013, Interaction of Medicago truncatula lysin motif receptor-like kinases, NFP and LYK3, produced in Nicotiana benthamiana induces defence-like responses, PLoS One, 8, e65055, 10.1371/journal.pone.0065055
Madsen, 2011, Autophosphorylation is essential for the in vivo function of the Lotus japonicus Nod factor receptor 1 and receptor-mediated signalling in cooperation with Nod factor receptor 5, Plant J, 65, 404, 10.1111/j.1365-313X.2010.04431.x
Larrainzar, 2015, Deep sequencing of the Medicago truncatula root transcriptome reveals a massive and early interaction between nodulation factor and ethylene signals, Plant Physiol, 169, 233, 10.1104/pp.15.00350
Maillet, 2011, Fungal lipochitooligosaccharide symbiotic signals in arbuscular mycorrhiza, Nature, 469, 58, 10.1038/nature09622
Bozsoki, 2017, Receptor-mediated chitin perception in legume roots is functionally separable from Nod factor perception, Proc Natl Acad Sci U S A, 114, 8118, 10.1073/pnas.1706795114
Kiirika, 2012, Silencing of the Rac1 GTPase MtROP9 in Medicago truncatula stimulates early mycorrhizal and oomycete root colonizations but negatively affects rhizobial infection, Plant Physiol, 159, 501, 10.1104/pp.112.193706
Wang, 2012, A common signaling process that promotes mycorrhizal and oomycete colonization of plants, Curr Biol, 22, 2242, 10.1016/j.cub.2012.09.043
Luginbuehl, 2017, Fatty acids in arbuscular mycorrhizal fungi are synthesized by the host plant, Science, 356, 1175, 10.1126/science.aan0081
Bravo, 2017, Arbuscular mycorrhiza-specific enzymes FatM and RAM2 fine-tune lipid biosynthesis to promote development of arbuscular mycorrhiza, New Phytol, 214, 1631, 10.1111/nph.14533
Jiang, 2017, Plants transfer lipids to sustain colonization by mutualistic mycorrhizal and parasitic fungi, Science, 356, 1172, 10.1126/science.aam9970
Keymer, 2017, Lipid transfer from plants to arbuscular mycorrhiza fungi, eLife, 6, e29107, 10.7554/eLife.29107
Rey, 2016, MtNF-YA1, a central transcriptional regulator of symbiotic nodule development, is also a determinant of Medicago truncatula susceptibility toward a root pathogen, Front Plant Sci, 7, 1837, 10.3389/fpls.2016.01837
Fonouni-Farde, 2016, DELLA-mediated gibberellin signalling regulates Nod factor signalling and rhizobial infection, Nat Commun, 7, 12636, 10.1038/ncomms12636
Baudin, 2015, A phylogenetically conserved group of nuclear factor-Y transcription factors interact to control nodulation in legumes, Plant Physiol, 169, 2761
Laporte, 2014, The CCAAT box-binding transcription factor NF-YA1 controls rhizobial infection, J Exp Bot, 65, 481, 10.1093/jxb/ert392
Floss, 2016, DELLA proteins regulate expression of a subset of AM symbiosis-induced genes in Medicago truncatula, Plant Signal Behav, 11, e1162369, 10.1080/15592324.2016.1162369
Park, 2015, Hyphal branching during arbuscule development requires reduced arbuscular mycorrhiza, Plant Physiol, 169, 2774
Xue, 2015, Network of GRAS transcription factors involved in the control of arbuscule development in Lotus japonicus, Plant Physiol, 167, 854, 10.1104/pp.114.255430
Kim, 2013, A novel GRAS protein gene MtSymSCL1 plays a role in regulating nodule number in Medicago truncatula, Plant Growth Regul, 71, 77, 10.1007/s10725-013-9814-7
Rey, 2017, The Medicago truncatula GRAS protein RAD1 supports arbuscular mycorrhiza symbiosis and Phytophthora palmivora susceptibility, J Exp Bot, 68, 5871, 10.1093/jxb/erx398
Jin, 2016, DELLA proteins are common components of symbiotic rhizobial and mycorrhizal signalling pathways, Nat Commun, 7, 12433, 10.1038/ncomms12433
Tatsukami, 2016, Rhizobial gibberellin negatively regulates host nodule number, Sci Rep, 6, 27998, 10.1038/srep27998
Yu, 2014, A DELLA protein complex controls the arbuscular mycorrhizal symbiosis in plants, Cell Res, 24, 130, 10.1038/cr.2013.167
Takeda, 2015, Gibberellins interfere with symbiosis signaling and gene expression and alter colonization by arbuscular mycorrhizal fungi in Lotus japonicus, Plant Physiol, 167, 545, 10.1104/pp.114.247700
De Bruyne, 2014, Connecting growth and defense: the emerging roles of brassinosteroids and gibberellins in plant innate immunity, Mol Plant, 7, 943, 10.1093/mp/ssu050
De Vleesschauwer, 2016, The DELLA protein SLR1 integrates and amplifies salicylic acid- and jasmonic acid-dependent innate immunity in rice, Plant Physiol, 170, 1831, 10.1104/pp.15.01515
Berens, 2017, Evolution of hormone signaling networks in plant defense, Annu Rev Phytopathol, 55, 401, 10.1146/annurev-phyto-080516-035544
Penmetsa, 2008, The Medicago truncatula ortholog of Arabidopsis EIN2, sickle, is a negative regulator of symbiotic and pathogenic microbial associations, Plant J, 55, 580, 10.1111/j.1365-313X.2008.03531.x
Laffont, 2015, The CRE1 cytokinin pathway is differentially recruited depending on Medicago truncatula root environments and negatively regulates resistance to a pathogen, PLoS One, 10, e0116819, 10.1371/journal.pone.0116819
Besserer, 2006, Strigolactones stimulate arbuscular mycorrhizal fungi by activating mitochondria, PLoS Biol, 4, e226, 10.1371/journal.pbio.0040226
Piisilä, 2015, The F-box protein MAX2 contributes to resistance to bacterial phytopathogens in Arabidopsis thaliana, BMC Plant Biol, 15, 53, 10.1186/s12870-015-0434-4
Foo, 2016, The role of strigolactones during plant interactions with the pathogenic fungus Fusarium oxysporum, Planta, 243, 1387, 10.1007/s00425-015-2449-3
Marzec, 2016, Strigolactones as part of the plant defence system, Trends Plant Sci, 21, 900, 10.1016/j.tplants.2016.08.010
Chen, 2017, The phenylalanine ammonia lyase gene ljpal1 is involved in plant defense responses to pathogens and plays diverse roles in Lotus japonicusvrhizobium symbioses, Mol Plant Microbe Interact, 30, 739, 10.1094/MPMI-04-17-0080-R
Venkateshwaran, 2015, A role for the mevalonate pathway in early plant symbiotic signaling, Proc Natl Acad Sci U S A, 112, 9781, 10.1073/pnas.1413762112
Le Fevre, 2015, Modulation of host cell biology by plant pathogenic microbes, Annu Rev Cell Dev Biol, 31, 201, 10.1146/annurev-cellbio-102314-112502
Nars, 2013, Aphanomyces euteiches cell wall fractions containing novel glucan-chitosaccharides induce defense genes and nuclear calcium oscillations in the plant host Medicago truncatula, PLoS One, 8, e75039, 10.1371/journal.pone.0075039
Nadal, 2017, An N-acetylglucosamine transporter required for arbuscular mycorrhizal symbioses in rice and maize, Nat Plants, 3, 17073, 10.1038/nplants.2017.73
Sun, 2015, Activation of symbiosis signaling by arbuscular mycorrhizal fungi in legumes and rice, Plant Cell, 27, 823, 10.1105/tpc.114.131326
Sánchez-Vallet, 2015, The battle for chitin recognition in plant–microbe interactions, FEMS Microbiol Rev, 39, 171, 10.1093/femsre/fuu003