摘要
本文主要以广州优势水稻稻瘟病菌小种ZC13(97-151a)和以CO39为背景的水稻近等基因系C101LAC为材料,研究水稻激发子与稻瘟病菌之间的互作关系。采用mRNA差异显示技术,将得到的可能差异条带进行重扩增和纯化,最后得到差异显著的条带,采用重复试验,对重复性好且稳定的部分条带利用pMD18-T载体及大肠杆菌DH5α进行克隆测序,NCBI比对分析,发现某些差异片段与水稻的激酶及锌指蛋白有较高的同源性。
In order to reveal the molecular mechanisms of interaction between elicitor and rice, experiments were conducted with C 101LAC, the near isogenic lines of rice sharing CO39 background inoculated with M. grisea and one strain 97-151a of race ZC13, one of the prevalent races office blast fimgus M. grisea in Guangdong province. Differential cDNA fragments were performed by differential display polymerase chain reaction (DD-PCR) technology. Then the differential cDNA fragments were recovered from the gels and reamplified and purified. These fragments were transformed to pMD18-T vector and E. coli DH5a and sequenced and analyzed in NCBI. It indicated zinc finger protein and receptor protein kinase possibly participate in rice disease resistance to rice blast.
出处
《分子植物育种》
CAS
CSCD
2006年第4期535-539,共5页
Molecular Plant Breeding
基金
广东省自然科学基金重点项目(No.010350)
广东省自然科学基金项目(No.980162)资助.
关键词
水稻
稻瘟病
激发子
差异显示
Rice, Magnaporthe grisea, Elicitor, Differential display