文献类型：期刊文献

中文题名：马氏珠母贝(Pinctada fucata)组织蛋白酶L基因的克隆与表达分析

英文题名：CLONING AND EXPRESSION ANALYSIS OF THE CATHEPSIN L GENE FROM PEARL OYSTER PINCTADA FUCATA

作者：王忠良[1,2];简纪常[1,3];鲁义善[1,3];丁燏[1,3];王蓓[1,3];陈刚[1,2];吴灶和[3,4]

机构：[1]广东海洋大学水产学院,湛江524088;[2]广东海洋大学南海水产经济动物增养殖重点实验室,湛江524088;[3]广东省水产经济动物病原生物学及流行病学重点实验室,湛江524088;[4]仲恺农业工程学院,广州510225

年份：2013

卷号：44

期号：6

起止页码：1604

中文期刊名：海洋与湖沼

外文期刊名：Oceanologia Et Limnologia Sinica

收录：CSTPCD、、北大核心2011、Scopus、北大核心、CSCD、CSCD2013_2014

基金：国家自然科学基金项目;31202023号;国家科技支撑计划课题;2012BAD17B00号

语种：中文

中文关键词：马氏珠母贝;组织蛋白酶L;cDNA末端快速扩增;实时荧光定量PCR

外文关键词：Pinctada fucata; cathepsin L; rapid amplification of cDNA ends （RACE）; fluorescent quantitativereal-time PCR

中文摘要：根据已构建的溶藻弧菌(Vibro alginolyticus)诱导的马氏珠母贝(Pinctada fucata)血淋巴cDNA差减文库得到的ESTs序列,应用cDNA末端快速扩增(RACE)技术成功克隆了其组织蛋白酶L基因(PFCatL),并对其进行了生物信息学分析;应用实时荧光定量PCR(Real-time PCR)技术,研究了PFCatL基因在溶藻弧菌刺激前后马氏珠母贝足、外套膜、鳃、闭壳肌等8个组织中的表达变化。结果表明,PFCatL基因cDNA全长2004bp,其中5′非编码区(5′-UTR)50bp,3′非编码区(3′-UTR)865bp,开放阅读框(ORF)1089bp,编码362个氨基酸,其分子量计算值(MW)为40.52kDa,理论等电点(IP)为5.20;生物信息学分析表明,PFCatL含有16个氨基酸残基组成的信号肽序列以及组织蛋白酶前体抑制功能域I29;Clustalw2多重比对发现PFCatL氨基酸序列在催化三联体Cys-His-Asn、底物结合位点以及二硫键形成相关的半胱氨酸残基位点高度保守;Real-time PCR研究发现,PFCatL在马氏珠母贝各组织中均有表达,但各组织间的表达量存在差异,其中以肾和闭壳肌中的表达量最高;溶藻弧菌感染4h后,外套膜、鳃以及血淋巴中PFCatL基因的表达较感染前显著上调。

外文摘要：To examine the expression patterns of the PFCatLgene in various tissues, including foot, mantle, gill, adductor, heart, kidney, hepatopancreas, and haemolymph of healthy and Vibrio alginolyticus challenged oyster Pinctada fucata, we cloned the cDNA of cathepsin L （PFCatL） in the oyster by rapid amplification cDNA ends （RACE） technique based on the ESTs that analyzed from SSH cDNA library, and employed fluorescent real-time quantitative PCR （RT-PCR）. The results show that the full length of PFCatLcDNA was 2004bp, including a 5＇ 50bp UTR, a 3＇ 865bp UTR, and a 1089bp ORF encoding a polypeptide of 362 amino acids with an MW at 40.52 kDa, and a 5.20 IP. A signal peptide of 16 amino acids and a peptidase inhibitor domain I29 were detected in PFCatLby SignalP and Prosite analysis. The catalytic triad, substrate binding sites, and cysteine disulfide linkage sites were highly conserved in PFCatL, indicated by multiple alignment analysis. PFCatLtranscripts were expressed ubiquitously in all tested tissues, while the expression levels were significantly different from each other; and the highest expression was detected in kidney and adductor. Four hours after injection with V. alginolyticus, the expression of PFCatLtranscripts in mantle, gill, and haemolymph of P. fucatawere significantly up-regulated relative to that of the control.