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Items: 1 to 50 of 51

1.

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.

2.

A GRAS-type transcription factor with a specific function in mycorrhizal signaling.

Gobbato E, Marsh JF, Vernié T, Wang E, Maillet F, Kim J, Miller JB, Sun J, Bano SA, Ratet P, Mysore KS, Dénarié J, Schultze M, Oldroyd GE.

Curr Biol. 2012 Dec 4;22(23):2236-41. doi: 10.1016/j.cub.2012.09.044. Epub 2012 Nov 1.

3.

Transcriptional responses toward diffusible signals from symbiotic microbes reveal MtNFP- and MtDMI3-dependent reprogramming of host gene expression by arbuscular mycorrhizal fungal lipochitooligosaccharides.

Czaja LF, Hogekamp C, Lamm P, Maillet F, Martinez EA, Samain E, Dénarié J, Küster H, Hohnjec N.

Plant Physiol. 2012 Aug;159(4):1671-85. doi: 10.1104/pp.112.195990. Epub 2012 May 31.

4.

The Medicago genome provides insight into the evolution of rhizobial symbioses.

Young ND, Debellé F, Oldroyd GE, Geurts R, Cannon SB, Udvardi MK, Benedito VA, Mayer KF, Gouzy J, Schoof H, Van de Peer Y, Proost S, Cook DR, Meyers BC, Spannagl M, Cheung F, De Mita S, Krishnakumar V, Gundlach H, Zhou S, Mudge J, Bharti AK, Murray JD, Naoumkina MA, Rosen B, Silverstein KA, Tang H, Rombauts S, Zhao PX, Zhou P, Barbe V, Bardou P, Bechner M, Bellec A, Berger A, Bergès H, Bidwell S, Bisseling T, Choisne N, Couloux A, Denny R, Deshpande S, Dai X, Doyle JJ, Dudez AM, Farmer AD, Fouteau S, Franken C, Gibelin C, Gish J, Goldstein S, González AJ, Green PJ, Hallab A, Hartog M, Hua A, Humphray SJ, Jeong DH, Jing Y, Jöcker A, Kenton SM, Kim DJ, Klee K, Lai H, Lang C, Lin S, Macmil SL, Magdelenat G, Matthews L, McCorrison J, Monaghan EL, Mun JH, Najar FZ, Nicholson C, Noirot C, O'Bleness M, Paule CR, Poulain J, Prion F, Qin B, Qu C, Retzel EF, Riddle C, Sallet E, Samain S, Samson N, Sanders I, Saurat O, Scarpelli C, Schiex T, Segurens B, Severin AJ, Sherrier DJ, Shi R, Sims S, Singer SR, Sinharoy S, Sterck L, Viollet A, Wang BB, Wang K, Wang M, Wang X, Warfsmann J, Weissenbach J, White DD, White JD, Wiley GB, Wincker P, Xing Y, Yang L, Yao Z, Ying F, Zhai J, Zhou L, Zuber A, Dénarié J, Dixon RA, May GD, Schwartz DC, Rogers J, Quétier F, Town CD, Roe BA.

Nature. 2011 Nov 16;480(7378):520-4. doi: 10.1038/nature10625.

5.

Fungal lipochitooligosaccharide symbiotic signals in arbuscular mycorrhiza.

Maillet F, Poinsot V, André O, Puech-Pagès V, Haouy A, Gueunier M, Cromer L, Giraudet D, Formey D, Niebel A, Martinez EA, Driguez H, Bécard G, Dénarié J.

Nature. 2011 Jan 6;469(7328):58-63. doi: 10.1038/nature09622.

PMID:
21209659
6.

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.

8.

A putative Ca2+ and calmodulin-dependent protein kinase required for bacterial and fungal symbioses.

Lévy J, Bres C, Geurts R, Chalhoub B, Kulikova O, Duc G, Journet EP, Ané JM, Lauber E, Bisseling T, Dénarié J, Rosenberg C, Debellé F.

Science. 2004 Feb 27;303(5662):1361-4. Epub 2004 Feb 12.

9.

Medicago truncatula DMI1 required for bacterial and fungal symbioses in legumes.

Ané JM, Kiss GB, Riely BK, Penmetsa RV, Oldroyd GE, Ayax C, Lévy J, Debellé F, Baek JM, Kalo P, Rosenberg C, Roe BA, Long SR, Dénarié J, Cook DR.

Science. 2004 Feb 27;303(5662):1364-7. Epub 2004 Feb 12.

10.

Plant sciences. How legumes select their sweet talking symbionts.

Cullimore J, Dénarié J.

Science. 2003 Oct 24;302(5645):575-8. No abstract available.

PMID:
14576408
11.

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.

Amor BB, Shaw SL, Oldroyd GE, Maillet F, Penmetsa RV, Cook D, Long SR, Dénarié J, Gough C.

Plant J. 2003 May;34(4):495-506. Erratum in: Plant J. 2003 Jul;35(1):140.

12.

A diffusible factor from arbuscular mycorrhizal fungi induces symbiosis-specific MtENOD11 expression in roots of Medicago truncatula.

Kosuta S, Chabaud M, Lougnon G, Gough C, Dénarié J, Barker DG, Bécard G.

Plant Physiol. 2003 Mar;131(3):952-62.

13.

Genetic and cytogenetic mapping of DMI1, DMI2, and DMI3 genes of Medicago truncatula involved in Nod factor transduction, nodulation, and mycorrhization.

Ané JM, Lévy J, Thoquet P, Kulikova O, de Billy F, Penmetsa V, Kim DJ, Debellé F, Rosenberg C, Cook DR, Bisseling T, Huguet T, Dénarié J.

Mol Plant Microbe Interact. 2002 Nov;15(11):1108-18.

14.

Nod genes and Nod signals and the evolution of the Rhizobium legume symbiosis.

Debellé F, Moulin L, Mangin B, Dénarié J, Boivin C.

Acta Biochim Pol. 2001;48(2):359-65. Review.

15.

Unusual methyl-branched alpha,beta-unsaturated acyl chain substitutions in the Nod Factors of an arctic rhizobium, Mesorhizobium sp. strain N33 (Oxytropis arctobia).

Poinsot V, Bélanger E, Laberge S, Yang GP, Antoun H, Cloutier J, Treilhou M, Dénarié J, Promé JC, Debellé F.

J Bacteriol. 2001 Jun;183(12):3721-8.

16.

The HCL gene of Medicago truncatula controls Rhizobium-induced root hair curling.

Catoira R, Timmers AC, Maillet F, Galera C, Penmetsa RV, Cook D, Dénarié J, Gough C.

Development. 2001 May;128(9):1507-18.

17.

Genetic analysis of calcium spiking responses in nodulation mutants of Medicago truncatula.

Wais RJ, Galera C, Oldroyd G, Catoira R, Penmetsa RV, Cook D, Gough C, Denarié J, Long SR.

Proc Natl Acad Sci U S A. 2000 Nov 21;97(24):13407-12.

18.

Four genes of Medicago truncatula controlling components of a nod factor transduction pathway.

Catoira R, Galera C, de Billy F, Penmetsa RV, Journet EP, Maillet F, Rosenberg C, Cook D, Gough C, Dénarié J.

Plant Cell. 2000 Sep;12(9):1647-66.

19.

The common nodulation genes of Astragalus sinicus rhizobia are conserved despite chromosomal diversity.

Zhang XX, Turner SL, Guo XW, Yang HJ, Debellé F, Yang GP, Dénarié J, Young JP, Li FD.

Appl Environ Microbiol. 2000 Jul;66(7):2988-95.

20.

Structure of the Mesorhizobium huakuii and Rhizobium galegae Nod factors: a cluster of phylogenetically related legumes are nodulated by rhizobia producing Nod factors with alpha,beta-unsaturated N-acyl substitutions.

Yang GP, Debellé F, Savagnac A, Ferro M, Schiltz O, Maillet F, Promé D, Treilhou M, Vialas C, Lindstrom K, Dénarié J, Promé JC.

Mol Microbiol. 1999 Oct;34(2):227-37.

21.

Nodule-inducing activity of synthetic Sinorhizobium meliloti nodulation factors and related lipo-chitooligosaccharides on alfalfa. Importance of the acyl chain structure.

Demont-Caulet N, Maillet F, Tailler D, Jacquinet JC, Promé JC, Nicolaou KC, Truchet G, Beau JM, Dénarié J.

Plant Physiol. 1999 May;120(1):83-92.

22.

Specific flavonoids promote intercellular root colonization of Arabidopsis thaliana by Azorhizobium caulinodans ORS571.

Gough C, Galera C, Vasse J, Webster G, Cocking EC, Dénarié J.

Mol Plant Microbe Interact. 1997 Jul;10(5):560-70.

23.

The common nodABC genes of Rhizobium meliloti are host-range determinants.

Roche P, Maillet F, Plazanet C, Debellé F, Ferro M, Truchet G, Promé JC, Dénarié J.

Proc Natl Acad Sci U S A. 1996 Dec 24;93(26):15305-10.

24.

The NodA proteins of Rhizobium meliloti and Rhizobium tropici specify the N-acylation of Nod factors by different fatty acids.

Debellé F, Plazanet C, Roche P, Pujol C, Savagnac A, Rosenberg C, Promé JC, Dénarié J.

Mol Microbiol. 1996 Oct;22(2):303-14.

PMID:
8930915
25.

Rhizobium lipo-chitooligosaccharide nodulation factors: signaling molecules mediating recognition and morphogenesis.

Dénarié J, Debellé F, Promé JC.

Annu Rev Biochem. 1996;65:503-35. Review.

PMID:
8811188
26.
27.
28.

Lipo-oligosaccharide signalling: the mediation of recognition and nodule organogenesis induction in the legume-Rhizobium symbiosis.

Dénarié J, Truchet G, Promé JC.

Biochem Soc Symp. 1994;60:51-60. Review. No abstract available.

PMID:
7639792
29.

Role of the Rhizobium meliloti nodF and nodE genes in the biosynthesis of lipo-oligosaccharidic nodulation factors.

Demont N, Debellé F, Aurelle H, Dénarié J, Promé JC.

J Biol Chem. 1993 Sep 25;268(27):20134-42.

30.

Lipo-oligosaccharide nodulation factors: a minireview new class of signaling molecules mediating recognition and morphogenesis.

Dénarié J, Cullimore J.

Cell. 1993 Sep 24;74(6):951-4. Review. No abstract available.

PMID:
8402884
31.

Broad-host-range Rhizobium species strain NGR234 secretes a family of carbamoylated, and fucosylated, nodulation signals that are O-acetylated or sulphated.

Price NP, Relić B, Talmont F, Lewin A, Promé D, Pueppke SG, Maillet F, Dénarié J, Promé JC, Broughton WJ.

Mol Microbiol. 1992 Dec;6(23):3575-84.

PMID:
1474899
32.

The Rhizobium, Bradyrhizobium, and Azorhizobium NodC proteins are homologous to yeast chitin synthases.

Debellé F, Rosenberg C, Dénarié J.

Mol Plant Microbe Interact. 1992 Sep-Oct;5(5):443-6.

PMID:
1472721
33.

The lipo-oligosaccharidic symbiotic signals of Rhizobium meliloti.

Roche P, Debellé F, Lerouge P, Vasse J, Truchet G, Promé JC, Dénarié J.

Biochem Soc Trans. 1992 May;20(2):288-91. Review. No abstract available.

PMID:
1397613
34.

Signaling and host range variation in nodulation.

Dénarié J, Debellé F, Rosenberg C.

Annu Rev Microbiol. 1992;46:497-531. Review.

PMID:
1444265
35.

Molecular basis of symbiotic host specificity in Rhizobium meliloti: nodH and nodPQ genes encode the sulfation of lipo-oligosaccharide signals.

Roche P, Debellé F, Maillet F, Lerouge P, Faucher C, Truchet G, Dénarié J, Promé JC.

Cell. 1991 Dec 20;67(6):1131-43.

PMID:
1760841
36.
37.

Symbiotic host-specificity of Rhizobium meliloti is determined by a sulphated and acylated glucosamine oligosaccharide signal.

Lerouge P, Roche P, Faucher C, Maillet F, Truchet G, Promé JC, Dénarié J.

Nature. 1990 Apr 19;344(6268):781-4.

PMID:
2330031
38.

Rhizobium meliloti host range nodH gene determines production of an alfalfa-specific extracellular signal.

Faucher C, Maillet F, Vasse J, Rosenberg C, van Brussel AA, Truchet G, Dénarié J.

J Bacteriol. 1988 Dec;170(12):5489-99.

39.

Interference between Rhizobium meliloti and Rhizobium trifolii nodulation genes: genetic basis of R. meliloti dominance.

Debellé F, Maillet F, Vasse J, Rosenberg C, de Billy F, Truchet G, Dénarié J, Ausubel FM.

J Bacteriol. 1988 Dec;170(12):5718-27.

40.

A plasmid of Rhizobium meliloti 41 encodes catabolism of two compounds from root exudate of Calystegium sepium.

Tepfer D, Goldmann A, Pamboukdjian N, Maille M, Lepingle A, Chevalier D, Dénarié J, Rosenberg C.

J Bacteriol. 1988 Mar;170(3):1153-61.

41.

Multiple host-specificity loci of the broad host-range Rhizobium sp. NGR234 selected using the widely compatible legume Vigna unguiculata.

Lewin A, Rosenberg C, H Meyer ZA, Wong CH, Nelson L, Manen JF, Stanley J, Dowling DN, Denarie J, Broughton WJ.

Plant Mol Biol. 1987 Nov;8(6):447-59. doi: 10.1007/BF00017990.

PMID:
24301307
42.

Assignment of symbiotic developmental phenotypes to common and specific nodulation (nod) genetic loci of Rhizobium meliloti.

Debellé F, Rosenberg C, Vasse J, Maillet F, Martinez E, Dénarié J, Truchet G.

J Bacteriol. 1986 Dec;168(3):1075-86.

43.

Identification of a Rhizobium meliloti pSym2011 region controlling the host specificity of root hair curling and nodulation.

Truchet G, Debellé F, Vasse J, Terzaghi B, Garnerone AM, Rosenberg C, Batut J, Maillet F, Dénarié J.

J Bacteriol. 1985 Dec;164(3):1200-10.

44.

Transfer of Rhizobium meliloti pSym genes into Agrobacterium tumefaciens: host-specific nodulation by atypical infection.

Truchet G, Rosenberg C, Vasse J, Julliot JS, Camut S, Denarie J.

J Bacteriol. 1984 Jan;157(1):134-42.

45.
46.

Genes controlling early and late functions in symbiosis are located on a megaplasmid in Rhizobium meliloti.

Rosenberg C, Boistard P, Dénarié J, Casse-Delbart F.

Mol Gen Genet. 1981;184(2):326-33.

PMID:
6949001
47.

Use of RP4 plasmids carrying bacteriophage Mu insertions in nitrogen fixing bacteria Klebsiella pneumoniae and Rhizobium meliloti.

Rosenberg C, Bergeron B, Julliot JS, Dénarié J.

Basic Life Sci. 1977;9:411-6. Review. No abstract available.

PMID:
336028
48.

Introduction of bacteriophage Mu into Pseudomonas solanacearum and Rhizobium meliloti using the R factor RP4.

Boucher C, Bergeron B, De Bertalmio MB, Dénarié J.

J Gen Microbiol. 1977 Jan;98(1):253-63.

PMID:
319201
49.

[Introduction of the bacteriophage Mu into a nitrogen-fixing strain Klebsiella pneumoniae M 5 a 1].

Rosenberg C, Dénarié J.

C R Acad Sci Hebd Seances Acad Sci D. 1976 Sep 13;283(4):423-5. French.

PMID:
825294
50.

[Transduction of a gene controlling the expression of nitrogen fixation in Rhizobium meliloti].

Kowalski M, Dénarié J.

C R Acad Sci Hebd Seances Acad Sci D. 1972 Jul 3;275(1):141-4. French. No abstract available.

PMID:
4631535

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