Watanabe, J. A., 1,2) M. Ikegawa 1,3), T. Yamada 1) & K. N. Watanabe 1,2)

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Fishing Genes from germplasm: Cloning, testing and use of gene-like fragments associated with root-knot nematode resistance in tuber-bearing Solanum genetic resources Patent: WO03/080838 A1 Watanabe, J. A., 1,2) M. Ikegawa 1,3), T. Yamada 1) & K. N. Watanabe 1,2) 1. Dept. Biotech. Sci., Kinki University, Uchita, Wakayama, Japan 2. Gene Research Center, Univ. of Tsukuba, Ibaraki, Japan 3. Nara Advanced Inst. for Sci. and Technol., Ikoma, Nara, Japan

Root-knot nematodes infest over 2000 plant species Mi is a known plant resistance gene to some Meloidogyne incognita

Root-knot nematode resistance genes in Potato RKN is an important pest in warm and tropical zones including Southern part of Japan such as Nagasaki 1) Original genetics lines developed (Watanabe et al. 1994) 2) Genetics and physiology of the trait analyzed well (Iwanaga et al. 1989, Watanabe et al. 1996, 1999) -> Quantitative, additive, temperature insensitive in phenotype. -> Broad range of reactions to different taxa of the nematode. 3) Diverse sources of resistances in various wild and cultivated species (Watanabe and Watanabe 2000) 4) Base work and patent filed in potatoes on markers(pct/jp02/12392)

Specific focuses Cloning gene-like fragments associated with rootknot nematode (Meloidogyne spp) resistance genes in potatoes Testing transgenic plants using the fragments Use of the gene information for diversity study and molecular breeding

Structure of Plant R genes (Science 292 #5525, Nature 411 #6839) Common Features in Plant R genes LZ: Leucine Zipper (Coiled coil) NBS: Nucleotide Binding Site LRR: Leucine-Rich Repeat TIR: Drosophila Toll and mammalian interleukin-1 recepter (IL-1R) homologous region PK: Protein Kinase Common Defense Mechanisms among Plants Signal Transduction Pathway: Nature 415:977-983, 2002

Common features in plant resistance genes T/S Kinases LZ(CC)/ TIR NBS LRR LRR: leucine rich repeats LZ: Leucine zipper/ CC: Coiled coil NBS:Nucleotide binding site TIR: Homologous region with Toll/IL-1R

Plasma membrane Intra cellar CC NBS LRR TIR NBS LRR RPM1, RPP2 N, L6, RPP5 avr gene LRR LRR Ser/Thr Protein Kinase CC Protein Kinase Pto/Fen Xa21 Cf-2, 4, 5, 9 RPW8 Categories of primary products from Plant disease resistance genes (Simplified from Dangl & Jones 2001, Science 411:826-827)

RKN resistance gene in Sweetpotato Similar structure to known plant R genes but not identical Variation occurs in hexasomic hexaploid genome Diversity among 6x genotypes Possibility of SNPs for identification of R/S Weak expression Need elaboration of transgenic manipulation I Base knowledge filed as patent (JP 2001-223606)

Materials Diploid potato breeding lines with high levels of resistance to RKN (Watanabe et al. 1996, 1999) Tetraploid potato cultivars with known S for comparison

Methods PCR:Primers designed from common motifs in PDR genes especially from Mi and sweetpotato information Cloning:Random cloning of PCR products Sequence comparison:difference between fragments from R and S genotypes Amino acid identity: with known PDR genes Construction of binary vector: pbi121 or pbe2113 Not Transformation: Agrobacterium tumefaciens LBA4404 Resistance evaluation: regenrants on N. benthamiana and Desiree

NBS region comparison 85.37.38 G M P G S G K T T L A Y R V Y N D K S V Beniazuma (SP) G M G G I G K T T L A E R V Y N D K A V Mi-1.1 G M P G S G K T T L A Y K V Y N D K S V Mi-1.2 G M P G S G K T T L A Y K V Y N D K S V PRF G M P G L G K T T L A K K I Y N D P E V I2C-1 G M G G M G K T T L A K A V Y N D E R V I2C-2 G M G G L G K T T L A K A V Y N D E R V RPM1 G M G G S G K T T L S A N V F K S Q S V N G M G G V G K T T I A R A L F D T L L G RPP5 G Q S G I G K S T L G R A F RPP2 G P G G V G K T T L L M S I ADG2 --------------------- Kinase 1a 85.37.38 I S S Y F D L H A W C T V S Q G H D E R Beniazuma (SP) I A S Y F D I R A W T T I S Q Q H N L R Mi-1.1 - S S R F D L R A W C T V D Q G C D E K Mi-1.2 - S R H F D L R A W C T V D Q G Y D D K PRF - T S R F D V H A W C T V D Q L Y S W R I2C-1 - Q K H F G L T A W F C V S E A Y D A F I2C-2 - K N H F D L K A W F C V S E A Y N A F RPM1 - R R H F E S Y A W V T I S K S Y V I E N - R M D RPP5 RPP2 ADG2

Deduced amino acid identity with known PDR genes Solanum acaule NBS-LRR protein 607/867 (70%) Solanum tuberosum RGC1 protein, 607/867 (70%) Solanum tuberosum NBS-LRR protein, 611/867 (70.5%) Solanum tuberosum disease resistance protein Gpa2 protein 611/867 (70.5%) Solanum tuberosum Rx protein protein 604/867 (70%) Capsicum chacoense disease resistance protein BS2 protein, 482/870 (55.4%) Lycopersicon esculentum PRF protein, 403/742 (54%) Lycopersicon pimpinellifolium PRF protein, 391/726 (54%) Lycopersicon esculentum root-knot nematode resistance protein, 410/816 (50%) Arabidopsis thaliana RPP13 protein, 338/682 (50%) Arabidopsis thaliana rpp8 protein, 399/822 (49%) Arabidopsis lyrata NBS/LRR disease resistance protein RPM1, 352/675 (52%)

Summary results of cloning and sequence study 2613 bps fragment containing NBS and LRR regions with incomplete CC Conserved in NBS and LRR, but not identical to known genes Mapped at Chrom VI of potato around Mi of tomato R & S alleles: probably stop codons at introns in S Variation in S alleles

1 2 3 4 5 6 7 8 9 2600bp RT-PCR using LRR region specific to the potato RKN gene 1. Marker, 2. N.bensamiana control, 3. And 4 transgenic plants, 5. S. tuberosum Susceptible control, 6 and 7 S. tuberosum donor, 8. And 9. Negative control

Resistance evaluation in N. benthamiana Root-knot nematodes (RKN) were maintained in soil pots with susceptible tomato genotypes. Minimum of five cuttings per line were used for the evaluation. Cuttings were made three weeks before transplanting to the RKN infested soil to let rooting enough. General infection method Iwanaga et al. (1989) except the incubation temperature of the plants were conducted between 30-35 degree Celsius at day temperature for 16 hours and 25-30 degree Celcius at night temperature for 8 hours at the controlled growth chambers.

Resistance evaluation Galls were scored in roots. Clones with only no galls were subjected to microscopic observation using erioglaucine (0.05% aqueous solution for 10 min, Yaghoobi et al. 1995) for egg observation. Further microscopic observation was conducted on the presence of adults.

Resistance scoring HR: No gall and no egg in root R: No gall and presence of some egg in root mass MR: Some galls @ specific root region and presence of eggs in root mass MS: Many galls @ specific root region S: Many galls over root system