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小麦NBS-LRR类抗病基因同源序列的分离与鉴定 被引量:14

CLONING AND IDENTIFICATION OF THE RESISTANCE GENE ANALOGS OF WHEAT
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摘要 根据已知植物抗病基因的保守区域设计引物,从抗锈病小麦品种西农88基因组DNA扩增出3条与植物抗病基因同源的序列,分别为WRGA1、WRGA2和WRGA14。这三条同源片段均含有典型的NBS-LRR类抗病基因所拥有的保守性结构域Kinase-2a、Kinase-3a和疏水结构域(HD).它们与部分已知NBS-LRR类抗病基因的氨基酸序列同源性为46.0%-9.9%,三个片段间在氨基酸水平上的同源性为80.7%-56.8%。Northern杂交表明WRGA1在小麦中受水杨酸正调控,属诱导型表达。 Specific primer sequences were designed on the basis of converse motifs of cloned resistance genes and subsequently used as PCR primers to amplify the resistance gene analog (RGA) in wheat (Triticum aestivum L.) Xinong 88 which possesses rust disease resistance. The amplified products of WRGA1,WRGA2 and WRGA14 were cloned and sequenced. The wheat RGAs contain some conserved motifs such as Kinase-2a,Kinase-3a and HD presenting in known NBS-LRR resistance genes from other plants and share between 46.0%-9.9% amino acid sequence identity with them. The amino acid sequence identity among three RGAs is 80.7%-56.8%. The WRGA1 expression was induced and detected by Northern blotting, which is positively regulated by salicylic acid.
出处 《分子细胞生物学报》 CSCD 北大核心 2006年第2期91-96,共6页 Journal of Molecular Cell Biology
基金 陕西省自然科学基金重点项目(2001SM24) 陕西省重点实验室科研计划项目(04JS07) 陕西省教育厅科学研究计划项目(05JK304)资助。
关键词 小麦 NBS—LRR 同源克隆技术 抗病基因同源序列 水杨酸 Wheat. NBS-LRR. Homology-based cloning. Resistance gene analog(RGA).Salicylic acid
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  • 1Johal,G. S. & S. P. Briggs, 1992, Reductase encode by the Hml disease resistance gene in maize. Science , 258:985-987.
  • 2Flor, H.H., 1971, Current status of the gene-for-gene concept. Annu. Rev. Phytopathol,9: 275-296.
  • 3Bakre, B., P. Zambryski, B. Staskawize & S. P. Dineshkumar, 1997, Signaling in plant microbe interactions.Science, 276:726-733.
  • 4Anderson, P. A., G. J. Lawrence, B. C. Morrish, M. A.Ayliffe, E. J. Finnegan & J. G. Ellis, 1997,Inactivation of the flax rust resistance gene M associated with loss of a repeated unit within the leucine-rich repeat coding region.Plant Cell, 9: 641-651.
  • 5Off,N., Y. Eshed, I. Paran, G. Presting, D. Aviv, S.Tanksley, D. Zamir & R. Fluhr, 1997 ,The 12C family from the wilt disease resistance locus 12 belongs to the nucleotide binding, leucine-rich repeat superfamily of plant resistance genes. Plant Cell, 9:521-532.
  • 6Mindrinos, M., F. Katagiri, G. L. Yu & F. M. Ausubel,1994, The A. thaliana disease resistance gene RPS2 encodes a protein containing a nucleotide-bending site and leucine-rich repeats. Cell, 78-1089-1099.
  • 7Yoshimura,S., U. Yamamouchi, Y. Katayose , S. Toki,Z. X. Wang, I. Kono, N. Kurata, M. Yano, N. Iwata & T. Sasaki, 1998, Expression of Xal, a bacterial blight resistance gene in rice, is induced by bacterial inoculation. Proc. Natl. Acad. Sci. U S A., 95:1663-1668.
  • 8Lagudah, E. S., O. Mouller & R. Appels, 1997, Map-based cloning of a gene sequence encoding a nucleotide-binding domain and a leucine-rich repeat region at the Cre3 nematode resistance locus of wheat. Genome, 40: 659-665.
  • 9Huang, L., S. A. Brooks, W. Li, J. P. Fellers, H. N. Trick & B. S. Gill, 2003, Map-based cloning of leaf rust resistance gene Lr21 from the large and polyploid genome of bread wheat. Genetics, 164: 655-664.
  • 10Feuillet,C., S. Travella, N. Stein, L. Albar, A. Nublat & B. Keller, 2003, Map-based isolation of the leaf rust disease resistance gene LrI0 from the hexaploid wheat(Triticum aestivum L) genome. Proc. Natl. Acad. Sci. U S A,100: 15253-15258.

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