Medicago truncatula symbiosis mutants affected in the interaction with a biotrophic root pathogen

New Phytologist

Volumn 206, Issue 2, 2015, Pages 497-500

  Rey, Thomas ^a   Chatterjee, Abhishek ^a   Buttay, Margaux ^a   Toulotte, Justine ^a   Schornack, Sebastian ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

Medicago truncatula; Phytophthora palmivora; Haustoria; Immunity; Root nodules; Symbiosis

Indexed keywords

FUNGAL DISEASE; IMMUNITY; LEGUME; MUTATION; NODULATION; ROOT SYSTEM; SYMBIOSIS;

MEDICAGO TRUNCATULA; PHYTOPHTHORA PALMIVORA;

BARREL MEDIC; DISEASE RESISTANCE; GENETICS; HOST PATHOGEN INTERACTION; IMMUNOLOGY; MICROBIOLOGY; MUTATION; PHYSIOLOGY; PHYTOPHTHORA; PLANT DISEASE; PLANT ROOT; SYMBIOSIS;

DISEASE RESISTANCE; HOST-PATHOGEN INTERACTIONS; MEDICAGO TRUNCATULA; MUTATION; PHYTOPHTHORA; PLANT DISEASES; PLANT ROOTS; SYMBIOSIS;

EID: 84925236395     PISSN: 0028646X     EISSN: 14698137     Source Type: Journal    
DOI: 10.1111/nph.13233     Document Type: Article

References (18)

1. Arrighi JF, Barre A, Ben Amor B, Bersoult A, Soriano LC, Mirabella R, de Carvalho-Niebel F, Journet EP, Ghérardi M, Huguet T et al. 2006. The Medicago truncatula lysin [corrected] motif-receptor-like kinase gene family includes NFP and new nodule-expressed genes. Plant Physiology 142: 265-279.
2. Bright LJ, Liang Y, Mitchell DM, Harris JM. 2005. The LATD gene of Medicago truncatula is required for both nodule and root development. Molecular Plant-Microbe Interactions 18: 521-532.
3. Cerri MR, Frances L, Laloum T, Auriac MC, Niebel A, Oldroyd GE, Barker DG, Fournier J, de Carvalho-Niebel F. 2012. Medicago truncatula ERN transcription factors: regulatory interplay with NSP1/NSP2 GRAS factors and expression dynamics throughout rhizobial infection. Plant Physiology 160: 2155-2172.
4. Czaja LF, Hogekamp C, Lamm P, Maillet F, Martinez EA, Samain E, Dénarié J, Küster H, Hohnjec N. 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 Physiology 159: 1671-1685.
5. Drenth A, Guest DI. 2004. Diversity and management of Phytophthora in Southeast Asia. Aciar Monograph Series 114. Canberra, ACT, Australia: Australian Centre for International Agricultural Research, 1-238.
6. Gobbato E, Marsh JF, Vernié T, Wang E, Maillet F, Kim J, Miller JB, Sun J, Bano SA, Ratet P et al. 2012. A GRAS-type transcription factor with a specific function in mycorrhizal signaling. Current Biology 22: 2236-2241.
7. Gobbato E, Wang E, Higgins G, Bano SA, Henry C, Schultze M, Oldroyd GE. 2013. RAM1 and RAM2 function and expression during arbuscular mycorrhizal symbiosis and Aphanomyces euteiches colonization. Plant Signaling & Behavior 8: e26049.
8. Hardham A. 2001. The cell biology behind Phytophthora pathogenicity. Australasian Plant Pathology 30: 91-98.
9. Kiss E, Oláh B, Kaló P, Morales M, Heckmann AB, Borbola A, Lózsa A, Kontár K, Middleton P, Downie JA et al. 2009. LIN, a novel type of U-box/WD40 protein, controls early infection by rhizobia in legumes. Plant Physiology 151: 1239-1249.
10. Kuppusamy KT, Endre G, Prabhu R, Penmetsa RV, Veereshlingam H, Cook DR, Dickstein R, Vandenbosch KA. 2004. LIN, a Medicago truncatula gene required for nodule differentiation and persistence of rhizobial infections. Plant Physiology 136: 3682-3691.
11. Liang Y, Mitchell DM, Harris JM. 2007. Abscisic acid rescues the root meristem defects of the Medicago truncatula latd mutant. Developmental Biology 304: 297-307.
12. Parniske M. 2000. Intracellular accommodation of microbes by plants: a common developmental program for symbiosis and disease? Current Opinion in Plant Biology 3: 320-328.
13. Rey T, Nars A, Bonhomme M, Bottin A, Huguet S, Balzergue S, Jardinaud MF, Bono JJ, Cullimore J, Dumas B et al. 2013. NFP, a LysM protein controlling Nod factor perception, also intervenes in Medicago truncatula resistance to pathogens. New Phytologist 198: 875-886.
14. Smit P, Limpens E, Geurts R, Fedorova E, Dolgikh E, Gough C, Bisseling T. 2007. Medicago LYK3, an entry receptor in rhizobial nodulation factor signaling. Plant Physiology 145: 183-191.
15. Vernié T, Moreau S, de Billy F, Plet J, Combier JP, Rogers C, Oldroyd G, Frugier F, Niebel A, Gamas P. 2008. EFD Is an ERF transcription factor involved in the control of nodule number and differentiation in Medicago truncatula. Plant Cell 20: 2696-2713.
16. Wang E, Schornack S, Marsh JF, Gobbato E, Schwessinger B, Eastmond P, Schultze M, Kamoun S, Oldroyd GE. 2012. A common signaling process that promotes mycorrhizal and oomycete colonization of plants. Current Biology 22: 2242-2246.
17. Yendrek CR, Lee YC, Morris V, Liang Y, Pislariu CI, Burkart G, Meckfessel MH, Salehin M, Kessler H, Wessler H et al. 2010. A putative transporter is essential for integrating nutrient and hormone signaling with lateral root growth and nodule development in Medicago truncatula. Plant Journal 62: 100-112.
18. Zhang C, Bousquet A, Harris JM. 2014. Abscisic acid and LATERAL ROOT ORGAN DEFECTIVE/NUMEROUS INFECTIONS AND POLYPHENOLICS modulate root elongation via reactive oxygen species in Medicago truncatula. Plant Physiology 166: 644-658.