摘要
[研究目的]克隆羊草的乙醛脱氢酶ALDH基因片段,研究该基因在不同条件下的表达情况。[方法]采用RT-PCR技术克隆羊草的ALDH基因片段,并对其核苷酸和氨基酸序列进行分析,采用RealTimeRT-PCR方法研究该基因的表达。[结果]获得了羊草的ALDH基因片段,长度为675bp,编码225aa。核苷酸序列比较表明,与水稻ALDH1a序列(AB037421)同源性为86%,与玉米RF2C(AF348413)同源性为85%。BLASTp分析,该序列与水稻、玉米、拟南芥的乙醛脱氢酶一致性分别高达87%、86%、60%,含有醛脱氢酶基因家族的保守结构域。RealTimeRT-PCR数据表明,在诱导条件下该基因的表达量呈先升高后降低的趋势。总体上来说,该基因对盐的响应要高于干旱和冷冻。[结论]成功获得了羊草ALDH基因片段,并研究了该基因的表达情况,为进一步克隆羊草ALDH全长基因奠定了基础。
[Objective]Aldehyde Dehydrogenase （ALDH） gene segment from Leymus Chinensis was cloned and the expression of it was researched under the different situations. [Method]ALDH gene segment was cloned by RT-PCR. The nucleotide and amino acid sequence of ALDH were analyzed. The expression of ALDH was researched by Real Time RT-PCR. [Result]ALDH gene segment was obtained which was 675bp and coding 225aa. The compare of nucleotide sequences indicated that it has 86% identity with rice ALDHla （AB037421）, and 85% identity with maize RF2C （AF348413）. By BLASTp Analysis, it shares 87%, 86% and 60% amino acid sequence identity with rice, maize and Arabidopsis thaliana ALDH, respectively, which containing conservation region of aldehyde dehydrogenase families. The data of Real Time RT-PCR indicated that the expression of ALDH was increased first, and then decreased under the inducing situations. As a whole, the responses of ALDH to salt and drought were much higher than to cold. [Conclusion]In this research, ALDH gene segment was obtained, and we researched the expression of ALDH. It established basis on cloning the soan of ALDH in Leyrnus Chinensis.
出处
《中国农学通报》
CSCD
2007年第6期115-120,共6页
Chinese Agricultural Science Bulletin
基金
黑龙江省重大攻关课题(GA06B103-10)
哈尔滨市培养学科后备带头人基金(2005AFXXJ027)
