Literature DB >> 9057330

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

F Han1, A Kleinhofs, A Kilian, S E Ullrich.   

Abstract

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 Hm1 homolog in rice (Y. Hihara, M. Umeda, C. Hara, Q. Liu, S. Aotsuka, K. Toriyama, and H. Uchimiya, unpublished) and HCTR activity in barley, wheat, oats and sorghum have been reported (R. B. Meeley and J. D. Walton, Plant Physiol. 97:1080-1086, 1993).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.

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Year:  1997        PMID: 9057330     DOI: 10.1094/MPMI.1997.10.2.234

Source DB:  PubMed          Journal:  Mol Plant Microbe Interact        ISSN: 0894-0282            Impact factor:   4.171


  4 in total

1.  Plant-pathogen microevolution: molecular basis for the origin of a fungal disease in maize.

Authors:  D S Multani; R B Meeley; A H Paterson; J Gray; S P Briggs; G S Johal
Journal:  Proc Natl Acad Sci U S A       Date:  1998-02-17       Impact factor: 11.205

2.  Enhanced dihydroflavonol-4-reductase activity and NAD homeostasis leading to cell death tolerance in transgenic rice.

Authors:  Mitsunori Hayashi; Hideyuki Takahashi; Katsunori Tamura; Jirong Huang; Li-Hua Yu; Maki Kawai-Yamada; Takafumi Tezuka; Hirofumi Uchimiya
Journal:  Proc Natl Acad Sci U S A       Date:  2005-04-29       Impact factor: 11.205

3.  A guardian of grasses: specific origin and conservation of a unique disease-resistance gene in the grass lineage.

Authors:  Anoop Sindhu; Satya Chintamanani; Amanda S Brandt; Michael Zanis; Steven R Scofield; Gurmukh S Johal
Journal:  Proc Natl Acad Sci U S A       Date:  2008-01-29       Impact factor: 11.205

4.  Structure-based computational study of two disease resistance gene homologues (Hm1 and Hm2) in maize (Zea mays L.) with implications in plant-pathogen interactions.

Authors:  Budheswar Dehury; Mahesh Chandra Patra; Jitendra Maharana; Jagajjit Sahu; Priyabrata Sen; Mahendra Kumar Modi; Manabendra Dutta Choudhury; Madhumita Barooah
Journal:  PLoS One       Date:  2014-05-21       Impact factor: 3.240

  4 in total

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