Cloning and mapping of a putative barley NADPH-dependent HC-toxin reductase.

The NADPH-dependent HC-toxin reductase (HCTR), encoded by Hm1 in maize, inactivates HC-toxin produced by the fungus Cochliobolus carbonum, and thus confers resistance to the pathogen. The fact that C. carbonum only infects maize (Zea mays) and is the only species known to produce HC-toxin raises the question: What are the biological functions of HCTR in other plant species? An HCTR-like enzyme may function to detoxify toxins produced by pathogens which infect other plant species (R. B. Meeley, G. S. Johal, S. E. Briggs, and J. D. Walton, Plant Cell, 4:71-77, 1992). Hm1 homolog in rice (Y. Hihara, M. Umeda, C. Hara, Q. Liu, S. Aotsuka, K. Toriyama, and H. Uchimiya, unpublished) and HCTR activity in barley, wheat, oats and sorghum have been reported (R. B. Meeley and J. D. Walton, Plant Physiol. 97:1080-1086, 1993). To investigate the sequence conservation of Hm1 and HCTR in barley and the possible relationship of barley Hm1 homolog to the known disease resistance genes, we cloned and mapped a barley (Hordeum vulgare) Hm1-like gene. A putative full-length cDNA clone, Bhm1-18, was isolated from a cDNA library consisting of mRNA from young leaves, inflorescences, and immature embryos. This 1,297-bp clone encodes 363 amino acids which show great similarity (81.6%) with the amino acid sequence of HM1 in maize. Two loci were mapped to barley molecular marker linkage maps with Bhm1-18 as the probe; locus A (Bhm1A) on the long arm of chromosome 1, and locus B (Bhm1B) on the short arm of chromosome 1 which is syntenic to maize chromosome 9 containing the Hm2 locus. The Bhm1-18 probe hybridized strongly to a Southern blot of a wide range of grass species, indicating high conservation of HCTR at the DNA sequence level among grasses. The HCTR mRNA was detected in barley roots, leaves, inflorescences, and immature embryos. The conservation of the HCTR sequence, together with its expression in other plant species (R. B. Meeley and J. D. Walton, Plant Physiol. 97:1080-1086, 1993), suggest HCTR plays an important functional role in other plant species.

[1]  R. L. Warner,et al.  Variation of nitrate reductase genes in selected grass species. , 1995, Genome.

[2]  D. Ad,et al.  Use of filtered pipet tips to elute DNA from agarose gels. , 1995 .

[3]  S. Lin,et al.  A 300 kilobase interval genetic map of rice including 883 expressed sequences , 1994, Nature Genetics.

[4]  C. Lamb Plant disease resistance genes in signal perception and transduction , 1994, Cell.

[5]  S. Tanksley,et al.  Comparative linkage maps of the rice and maize genomes. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[6]  J. Walton,et al.  The cyclic peptide synthetase catalyzing HC-toxin production in the filamentous fungus Cochliobolus carbonum is encoded by a 15.7-kilobase open reading frame. , 1992, The Journal of biological chemistry.

[7]  S. Briggs,et al.  Reductase activity encoded by the HM1 disease resistance gene in maize. , 1992, Science.

[8]  J. Walton,et al.  A cyclic peptide synthetase gene required for pathogenicity of the fungus Cochliobolus carbonum on maize. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[9]  S. Briggs,et al.  A Biochemical Phenotype for a Disease Resistance Gene of Maize. , 1992, The Plant cell.

[10]  R. Meeley,et al.  Enzymatic Detoxification of HC-toxin, the Host-Selective Cyclic Peptide from Cochliobolus carbonum. , 1991, Plant physiology.

[11]  N. Scrutton,et al.  New enzymes for old: Redesigning the coenzyme and substrate specificities of glutathione reductase , 1991, BioEssays : news and reviews in molecular, cellular and developmental biology.

[12]  J. Walton Two enzymes involved in biosynthesis of the host-selective phytotoxin HC-toxin. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[13]  M. Daly,et al.  MAPMAKER: an interactive computer package for constructing primary genetic linkage maps of experimental and natural populations. , 1987, Genomics.

[14]  J. Devereux,et al.  A comprehensive set of sequence analysis programs for the VAX , 1984, Nucleic Acids Res..

[15]  R. B. Pringle Comparative biochemistry of the phytopathogenic fungus Helminthosporium. XVI. The production of victoxinine by H. sativum and H. victoriae. , 1976, Canadian journal of biochemistry.

[16]  C. Fyfe,et al.  Potential energy calculations of the mechanisms of self-diffusion in molecular crystals: adamantane , 1976 .

[17]  A. J. Ullstrup,et al.  RESISTANCE TO LEAF SPOT IN MAIZEGenetic Control of Resistance to Race I of Helminthosporium carbonum Ull , 1964 .

[18]  S. Tamura,et al.  Isolation of Helminthosporol as a Natural Plant Growth Regulator and its Chemical Structure , 1963 .

[19]  P. D. Mayo,et al.  The Constitution of Helminthosporal , 1962 .

[20]  A. J. Ullstrup,et al.  Linkage Relationships of a Gene in Corn Determining Susceptibility to a Helminthosporium Leaf Spot 1 , 1947 .

[21]  L. Dunkle,et al.  Analysis of Cochliobolus carbonum races by PCR amplification with arbitrary and gene-specific primers. , 1993 .

[22]  R. Scheffer Ecological Consequences of Toxin Production by Cochliobolus and Related Fungi , 1989 .

[23]  J. Walton,et al.  Properties of two enzymes involved in the biosynthesis of the fungal pathogenicity factor HC-toxin , 1988 .

[24]  R. Scheffer Host-specific Toxins in Relation to Pathogenesis and Disease Resistance , 1976 .