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蚕豆保卫细胞中ABA响应蛋白基因的转录
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作者 沈黎明 《植物生理学报(0257-4829)》 CSCD 1997年第3期288-292,共5页
Guard cells of V. faba were prepared by sonicating epidermal Peels andtreated with ABA, mannitol and Ca2+.RNAs extracted from leaf tissue andguard cells were hybridized with RNAprobes of several representative RABgene... Guard cells of V. faba were prepared by sonicating epidermal Peels andtreated with ABA, mannitol and Ca2+.RNAs extracted from leaf tissue andguard cells were hybridized with RNAprobes of several representative RABgenes. An RNA with a sequence cognated to Pea dehydrin (psdhn1 ) was detected in water-stressed leaves and inthe guard cells treated with ABA for 1and 6 h (Figs. 1 & 2). No RNA cognate to osmotin gene was detected in either tissue preparation. No differencewas found between the transcripts ofRAB genes from whole leaves and thosefrom guard cells (Fig. 1). ABA, butnot Ca2+, was required for the formation of sequence cognated to psdhn1 inguard cells. Exogenous osmotun did notpromote the formation of the RNA sequence. 展开更多
关键词 蚕豆 保卫细胞 脱落酸 响应蛋白基因 转录
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极端耐盐植物盐穗木脱水胁迫响应基因Rd22的克隆及表达分析 被引量:4
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作者 张霞 常丹 +1 位作者 彭丹 张富春 《生物技术》 CAS CSCD 北大核心 2013年第6期5-8,共4页
目的:选择合适的标记基因用于检测胁迫处理盐穗木的有效性。方法:根据NCBI同源序列比对设计简并引物,通过RT-PCR从盐穗木(Halostachys caspica)中克隆获得盐穗木脱水胁迫响应基因Rd22(HcRd22)基因,并采用实时定量PCR技术检测其逆境胁迫... 目的:选择合适的标记基因用于检测胁迫处理盐穗木的有效性。方法:根据NCBI同源序列比对设计简并引物,通过RT-PCR从盐穗木(Halostachys caspica)中克隆获得盐穗木脱水胁迫响应基因Rd22(HcRd22)基因,并采用实时定量PCR技术检测其逆境胁迫下的表达规律。结果:最终扩增获得301bp盐穗木HcRd22核酸序列,NCBI和clustalwz序列比对分析表明HcRd22具有BURP结构域。400 mmol/L盐胁迫和50μmol/L ABA处理分别使HcRd22的基因表达量在处理12h上调2.5倍和3倍。结论:所克隆的HcRd22基因属于盐胁迫和ABA处理的响应基因,可作为今后研究盐穗木胁迫处理的标准基因。 展开更多
关键词 盐穗木 脱水胁迫响应蛋白基因Rd22 同源克隆 实时定量PCR
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