A 500-bp cDNA fragment was amplified via RT-PCR from drought-induced total RNA of the drought-tolerant B. crassifolia Hemsl. using primers based on the sequence of published dehydrin conserved region. By using 5’ RAC...A 500-bp cDNA fragment was amplified via RT-PCR from drought-induced total RNA of the drought-tolerant B. crassifolia Hemsl. using primers based on the sequence of published dehydrin conserved region. By using 5’ RACE, full-length coding region (1 148 bp) of BDN1 gene was produced. It is a new member of the dehydrin gene family. Southern analysis indicated that BDN1 is present in the 6. crassifolia genome as a single-copy gene. Northern analysis revealed that its expression is inducible by drought and cold stresses as well as ABA application.展开更多
通过RT-PCR程序,从经过SA诱导的厚叶悬蒴苣苔中获得含WRKY家族保守序列的一条cDNA片段。运用RACE(Rapid Amplification of cDNA Ends)技术获得全长1803bp的cDNA克隆,名之为BcWRKY1。序列分析表明:BcWRKY1与甘薯SPF1[D30038]相似性最高,...通过RT-PCR程序,从经过SA诱导的厚叶悬蒴苣苔中获得含WRKY家族保守序列的一条cDNA片段。运用RACE(Rapid Amplification of cDNA Ends)技术获得全长1803bp的cDNA克隆,名之为BcWRKY1。序列分析表明:BcWRKY1与甘薯SPF1[D30038]相似性最高,保守区同源性达到84%。初步的Northern杂交分析表明:干旱、低温、高盐等逆境胁迫和外加SA、MeJA、JA、ABA等信号分子的诱导均能提高BcWRKY1基因的表达。但是表达情况各不相同。150mmol/L NaCl对BcWRKY1的诱导作用尤为明显和迅速。2168bp的BcWRKY1的基因组DNA克隆亦已获得,序列分析表明它含有4个内含子。展开更多
文摘A 500-bp cDNA fragment was amplified via RT-PCR from drought-induced total RNA of the drought-tolerant B. crassifolia Hemsl. using primers based on the sequence of published dehydrin conserved region. By using 5’ RACE, full-length coding region (1 148 bp) of BDN1 gene was produced. It is a new member of the dehydrin gene family. Southern analysis indicated that BDN1 is present in the 6. crassifolia genome as a single-copy gene. Northern analysis revealed that its expression is inducible by drought and cold stresses as well as ABA application.
