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作 者:张通[1] 周燕妮[1] 李长江[1] 张凌云[1]
机构地区:[1]北京林业大学,省部共建森林培育与保护教育部重点实验室,北京100083
出 处:《南京林业大学学报(自然科学版)》2014年第4期34-38,共5页Journal of Nanjing Forestry University:Natural Sciences Edition
基 金:国家自然科学基金面上项目(31270663);国家转基因生物新品种培育科技重大专项(2013ZX08009-003-002)
摘 要:色氨酸阻遏结合蛋白(tryptophan repressor-binding protein,WrbA)是一种重要的抗氧化酶类,参与了多种逆境反应。笔者通过RACE-PCR的方法克隆得到青杄WrbA基因的cDNA全长,共1 045 bp,编码区651 bp,编码203个氨基酸。利用生物信息学工具对其进行理化性质、二级结构和三级结构的分析,该蛋白理论分子质量21.80 ku,pI值6.43,N端11—15位氨基酸和C端112—165位氨基酸是FMN结合位点。荧光定量PCR和半定量RT-PCR发现青杄PwWrbA在各组织中都有表达,但在针叶中表达量最高。同时,PwWrbA在NaCl和ABA胁迫处理后表达量升高,H2O2也会影响其表达的改变,H2O2处理6 h后表达量上调。因此,PwWrbA是一个新的WrbA基因,推测其可能在青杄逆境胁迫应答中发挥作用。The tryptophan( W) repressor-binding protein( WrbA) is an important antioxidant enzyme which has been shown to play roles in a variety of adversities. In this study,PwWrbA cDNA was cloned by RACE-PCR method. Bioinformatics analysis showed that the full length of PwWrbA cDNA was 1 045 bp,including the ORF 651 bp,encoding 203 amino acids. The theoretical molecular weight was 21. 80 ku and value of pI was 6. 43. The ScanProsite online software showed that the N terminal 11- 15 aa and the C terminal 112- 165 aa were supposed to be the FMN binding sites. RTqPCR and semi-quantitative RT-PCR analysis showed PwWrbA expressed in various tissues,while the highest expression level was in pollen. Meanwhile,the expression of PwWrbA increased gradually after stress treatment with NaCl and ABA.In contrast to NaCl and ABA treatment,the expression of PwWrbA decreased in early stage and increased at 6 h after H2O2treatment. Our results suggested that PwWrbA was a new WrbA gene and played roles during different abiotic stresses.
关 键 词:青杄 WrbA基因 生物信息学 组织表达 胁迫响应
分 类 号:Q78[生物学—分子生物学] S792[农业科学—林木遗传育种]
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