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Items: 1 to 20 of 77

1.

Lipo-chitooligosaccharidic symbiotic signals are recognized by LysM receptor-like kinase LYR3 in the legume Medicago truncatula.

Fliegmann J, Canova S, Lachaud C, Uhlenbroich S, Gasciolli V, Pichereaux C, Rossignol M, Rosenberg C, Cumener M, Pitorre D, Lefebvre B, Gough C, Samain E, Fort S, Driguez H, Vauzeilles B, Beau JM, Nurisso A, Imberty A, Cullimore J, Bono JJ.

ACS Chem Biol. 2013 Sep 20;8(9):1900-6. doi: 10.1021/cb400369u. Epub 2013 Jul 5.

PMID:
23808871
2.

Molecular basis of lipo-chitooligosaccharide recognition by the lysin motif receptor-like kinase LYR3 in legumes.

Malkov N, Fliegmann J, Rosenberg C, Gasciolli V, Timmers AC, Nurisso A, Cullimore J, Bono JJ.

Biochem J. 2016 May 15;473(10):1369-78. doi: 10.1042/BCJ20160073. Epub 2016 Mar 17.

PMID:
26987814
3.

LYR3, a high-affinity LCO-binding protein of Medicago truncatula, interacts with LYK3, a key symbiotic receptor.

Fliegmann J, Jauneau A, Pichereaux C, Rosenberg C, Gasciolli V, Timmers AC, Burlet-Schiltz O, Cullimore J, Bono JJ.

FEBS Lett. 2016 May;590(10):1477-87. doi: 10.1002/1873-3468.12191. Epub 2016 May 17.

4.
5.

Lipo-chitooligosaccharide signaling in endosymbiotic plant-microbe interactions.

Gough C, Cullimore J.

Mol Plant Microbe Interact. 2011 Aug;24(8):867-78. doi: 10.1094/MPMI-01-11-0019. Review.

6.

Combined genetic and transcriptomic analysis reveals three major signalling pathways activated by Myc-LCOs in Medicago truncatula.

Camps C, Jardinaud MF, Rengel D, Carrère S, Hervé C, Debellé F, Gamas P, Bensmihen S, Gough C.

New Phytol. 2015 Oct;208(1):224-40. doi: 10.1111/nph.13427. Epub 2015 Apr 28.

7.

Interaction of Medicago truncatula lysin motif receptor-like kinases, NFP and LYK3, produced in Nicotiana benthamiana induces defence-like responses.

Pietraszewska-Bogiel A, Lefebvre B, Koini MA, Klaus-Heisen D, Takken FL, Geurts R, Cullimore JV, Gadella TW.

PLoS One. 2013 Jun 4;8(6):e65055. doi: 10.1371/journal.pone.0065055. Print 2013.

8.

Nod factor perception protein carries weight in biotic interactions.

Gough C, Jacquet C.

Trends Plant Sci. 2013 Oct;18(10):566-74. doi: 10.1016/j.tplants.2013.06.001. Epub 2013 Jul 10. Review.

PMID:
23850222
9.

Contribution of NFP LysM domains to the recognition of Nod factors during the Medicago truncatula/Sinorhizobium meliloti symbiosis.

Bensmihen S, de Billy F, Gough C.

PLoS One. 2011;6(11):e26114. doi: 10.1371/journal.pone.0026114. Epub 2011 Nov 8.

10.

The Medicago truncatula lysin [corrected] motif-receptor-like kinase gene family includes NFP and new nodule-expressed genes.

Arrighi JF, Barre A, Ben Amor B, Bersoult A, Soriano LC, Mirabella R, de Carvalho-Niebel F, Journet EP, Ghérardi M, Huguet T, Geurts R, Dénarié J, Rougé P, Gough C.

Plant Physiol. 2006 Sep;142(1):265-79. Epub 2006 Jul 14. Erratum in: Plant Physiol. 2007 Feb;143(2):1078.

11.

Evolution of a symbiotic receptor through gene duplications in the legume-rhizobium mutualism.

De Mita S, Streng A, Bisseling T, Geurts R.

New Phytol. 2014 Feb;201(3):961-72. doi: 10.1111/nph.12549. Epub 2013 Oct 28.

12.

Rhizobium Lipo-chitooligosaccharide Signaling Triggers Accumulation of Cytokinins in Medicago truncatula Roots.

van Zeijl A, Op den Camp RH, Deinum EE, Charnikhova T, Franssen H, Op den Camp HJ, Bouwmeester H, Kohlen W, Bisseling T, Geurts R.

Mol Plant. 2015 Aug;8(8):1213-26. doi: 10.1016/j.molp.2015.03.010. Epub 2015 Mar 21.

13.

Activation of symbiosis signaling by arbuscular mycorrhizal fungi in legumes and rice.

Sun J, Miller JB, Granqvist E, Wiley-Kalil A, Gobbato E, Maillet F, Cottaz S, Samain E, Venkateshwaran M, Fort S, Morris RJ, Ané JM, Dénarié J, Oldroyd GE.

Plant Cell. 2015 Mar;27(3):823-38. doi: 10.1105/tpc.114.131326. Epub 2015 Feb 27.

14.

Knowing your friends and foes--plant receptor-like kinases as initiators of symbiosis or defence.

Antolín-Llovera M, Petutsching EK, Ried MK, Lipka V, Nürnberger T, Robatzek S, Parniske M.

New Phytol. 2014 Dec;204(4):791-802. doi: 10.1111/nph.13117. Review.

15.

A novel nuclear protein interacts with the symbiotic DMI3 calcium- and calmodulin-dependent protein kinase of Medicago truncatula.

Messinese E, Mun JH, Yeun LH, Jayaraman D, Rougé P, Barre A, Lougnon G, Schornack S, Bono JJ, Cook DR, Ané JM.

Mol Plant Microbe Interact. 2007 Aug;20(8):912-21.

16.

Annexins - calcium- and membrane-binding proteins in the plant kingdom: potential role in nodulation and mycorrhization in Medicago truncatula.

Talukdar T, Gorecka KM, de Carvalho-Niebel F, Downie JA, Cullimore J, Pikula S.

Acta Biochim Pol. 2009;56(2):199-210. Epub 2009 May 7. Review.

17.

Role of N-glycosylation sites and CXC motifs in trafficking of medicago truncatula Nod factor perception protein to plasma membrane.

Lefebvre B, Klaus-Heisen D, Pietraszewska-Bogiel A, Hervé C, Camut S, Auriac MC, Gasciolli V, Nurisso A, Gadella TW, Cullimore J.

J Biol Chem. 2012 Mar 30;287(14):10812-23. doi: 10.1074/jbc.M111.281634. Epub 2012 Feb 9.

18.

A novel RNA-binding peptide regulates the establishment of the Medicago truncatula-Sinorhizobium meliloti nitrogen-fixing symbiosis.

Laporte P, Satiat-Jeunemaître B, Velasco I, Csorba T, Van de Velde W, Campalans A, Burgyan J, Arevalo-Rodriguez M, Crespi M.

Plant J. 2010 Apr 1;62(1):24-38. doi: 10.1111/j.1365-313X.2009.04121.x. Epub 2009 Dec 23.

19.

Lipo-chitin oligosaccharides, plant symbiosis signalling molecules that modulate mammalian angiogenesis in vitro.

Djordjevic MA, Bezos A, Susanti, Marmuse L, Driguez H, Samain E, Vauzeilles B, Beau JM, Kordbacheh F, Rolfe BG, Schwörer R, Daines AM, Gresshoff PM, Parish CR.

PLoS One. 2014 Dec 23;9(12):e112635. doi: 10.1371/journal.pone.0112635. eCollection 2014.

20.

Biochemical and phylogenetic analysis of CEBiP-like LysM domain-containing extracellular proteins in higher plants.

Fliegmann J, Uhlenbroich S, Shinya T, Martinez Y, Lefebvre B, Shibuya N, Bono JJ.

Plant Physiol Biochem. 2011 Jul;49(7):709-20. doi: 10.1016/j.plaphy.2011.04.004. Epub 2011 Apr 9.

PMID:
21527207

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