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    • 2. 发明申请
    • RESISTANCE GENE
    • 抗性基因
    • WO0140512A3
    • 2001-10-25
    • PCT/GB0004562
    • 2000-11-29
    • PLANT BIOSCIENCE LTDUS HEALTHUNIV IOWA STATE RES FOUND INCSCHULZE LEFERT PAUL MARIA JOSEKURTH JOACHIMFASONG ZHOUELLIOTT CANDACEWISE ROGER PHILIPHALTERMAN DENNIS ALLENWEI FUSHENG
    • SCHULZE-LEFERT PAUL MARIA JOSEKURTH JOACHIMFASONG ZHOUELLIOTT CANDACEWISE ROGER PHILIPHALTERMAN DENNIS ALLENWEI FUSHENG
    • C07K14/415C12N15/82C12Q1/68C12N15/29A01H5/00
    • C12N15/8282C07K14/415C12Q1/6895C12Q2600/13C12Q2600/156
    • Disclosed are isolated nucleic acid molecules which comprise an M1a nucleotide sequence derived form an M1a locus (e.g. M1a1 , 6, 12) encoding an MLA polypeptide which is capable of recognising and activating a race specific defence response in a plant into which the nucleic acid is introduced and expressed, in response to challenge with a cognate Erysiphe graminis isolate. Also disclosed are novel methods for selecting such sequences based on the determination of an M1a (AT)n micro-satellite identified by the present inventors. Also provided is an novel (3) component activity assay, for assessing the ability of nucleic acid encoding a putative resistance (R) gene to confer resistance against a pathogen expressing a cognate AVR gene, which comprises the steps of: (a) selecting plant material which comprises plant cells which express a recessive gene conferring resistance against the pathogen, (b) introducing into the plant material, nucleic acid encoding (i) a detectable marker, (ii) a dominant susceptibility gene which inhibits the resistance conferred by the recessive gene, and (iii) the putative R gene, (c) challenging the plant material with the pathogen, (d) observing cells in the plant material in which the marker is expressed to determine the amount of pathogen growth present, and (e) correlating the amount of pathogen growth with the ability of the R gene to confer resistance against the pathogen. Also provided are corresponding methods and materials (e.g. vectors, polypeptides, plants, kits) based on the use of M1a nucleotide sequences or identification methods.
    • 公开了分离的核酸分子,其包含编码MLA多肽的M1a基因座(例如M1a1,6,12)衍生的M1a核苷酸序列,所述MLA多肽能够识别和活化 在引入和表达核酸的植物中的种族特异性防御​​反应,响应于用同源物禾谷类分枝杆菌分离物进行攻击。 还公开了用于基于由本发明人识别的M1a(AT)n微卫星的确定来选择这种序列的新颖方法。 还提供了用于评估编码推定的抗性(R)基因的核酸赋予针对表达同源AVR基因的病原体的抗性的能力的新型(3)组分活性测定法,其包括以下步骤:(a)选择植物 (b)将编码(i)可检测标记,(ii)显性易感基因的核酸导入植物材料中,所述显性易感基因抑制由隐性基因所赋予的抗性 基因和(iii)推定的R基因,(c)用病原体攻击植物材料,(d)观察表达标记物的植物材料中的细胞以确定存在的病原体生长量,以及(e) 将病原体生长量与R基因赋予针对病原体的抗性的能力相关联。 还提供了基于使用M1a核苷酸序列或鉴定方法的相应方法和材料(例如载体,多肽,植物,试剂盒)。