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作 者:孟凡荣[1] 冉彩华[1] 刘浩[1] 陈雷[2] 李金花[2] 尹钧[2] 李永春[2]
机构地区:[1]河南农业大学生命科学学院,郑州450002 [2]河南农业大学国家小麦工程技术研究中心,郑州450002
出 处:《植物生理学通讯》2010年第7期671-676,共6页Plant Physiology Communications
基 金:国家转基因生物新品种培育科技重大专项(2009ZX08002-011B);河南省教育厅自然科学研究计划(2009A210012)
摘 要:在水分胁迫反应基因表达谱分析的基础上,采用RACR技术,从‘洛旱2号’小麦中克隆了一个编码富含亮氨酸蛋白的cDNA全长,命名为TaLRI1。序列分析显示,TaLRI1的cDNA全长为2657bp(GenBank登录号为GU593320),其中5'-非翻译区47bp,3'-非翻译区1314bp,开放阅读框1296bp,可编码431个氨基酸。进一步分析显示,TaLRI1基因编码的蛋白具有典型的富含亮氨酸N末端保守域和富含亮氨酸的核酸酶抑制因子保守域,该蛋白为弱酸性蛋白,等电点为5.69,无明显的疏水/亲水区域。三维结构预测显示,TaLRI1蛋白以α-螺旋、β-折叠和无规卷曲为骨架,可形成弧状的螺线管结构以及一对侧臂凸起。RT-PCR分析表明,水分胁迫过程中,TaLRI1基因在根系中的表达量呈先升高后降低的趋势,以胁迫处理12h的表达量最高,推测该基因在水分胁迫反应过程中发挥重要功能。Based on our previous study on the water stress responsive transcriptomes in wheat,a full-length cDNA,encoding a leucine-rich repeat (LRR) protein,was cloned via rapid amplification of cDNA ends (RACE) technology from the wheat (Triticum aestivum) cultivar 'Luohan 2',which was termed as TaLRI1 with the GenBank accession No.of GU593320.Sequence analysis showed that the full-length cDNA of TaLRI1 was 2 657 bp,which including 47 bp 5' UTR,1 314 bp 3' UTR and 1 296 bp open reading frame (ORF) encoding 431 amino acid residues.The further analysis indicated that a typical LRR N-terminal domain and a LRR ribonuclease inhibitor (LRR_RI) domain was included in the deduced amino acid sequence of TaLRI1.The putative TaLRI1 protein was acidulous with a pI of 5.69 and obvious hydrophobic or hydrophilic domains were not found in it.The 3D structure prediction showed that the TaLRI1 was constructed by α-helixes,β-strands and random loops,and could wrap around in a curved,right-handed solenoid with a pair of extended side arms.The expression pattern of TaLRI1 in roots under water stress was analyzed via RT-PCR and the results showed that the gene was gradually induced with the water-stress accumulation,while its expression level decreased after 12 h after water-stress treatment,which indicated that the TaLRI1 played important roles during the water-stress responding in wheat.
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