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引用本文:刘维青,倪多娇,宋林生,吴龙涛,胥炜,孔晓瑜.海湾扇贝(Argopecten irradians)金属硫蛋白基因的克隆与分析.海洋与湖沼,2006,37(5):444-449.
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海湾扇贝(Argopecten irradians)金属硫蛋白基因的克隆与分析
刘维青1,2, 倪多娇1, 宋林生1, 吴龙涛1, 胥炜1, 孔晓瑜3
1.中国科学院海洋研究所实验海洋生物学重点实验室 青岛266071;2.中国海洋大学水产学院 青岛266003;3.中国海洋大学水产学院青岛266003
摘要:
金属硫蛋白是一种普遍存在于生物体内的低分子量、半胱氨酸含量丰富、易于被外界刺激诱导的金属结合蛋白。采用表达序列标签法,结合cDNA末端快速扩增技术,首次获得了海湾扇贝金属硫蛋白(AiMT)的全长cDNA序列。该序列全长787bp,5′UTR(UntranslatedRegion)为79bp,3′UTR为270bp,开放阅读框(OpenReadingFrame,ORF)长度为438bp,可编码145个氨基酸。在其编码的氨基酸序列中半胱氨酸含量丰富,甘氨酸含量也较高,芳香族氨基酸含量低,不含组氨酸,存在有无脊椎动物和软体动物金属硫蛋白的特征序列CKCXXX-CXCX,C-末端的氨基酸序列也符合软体动物金属硫蛋白标签序列C-x-C-x(3)-C-T-G-x(3)-C-x-C-x(3)-C-x-C-K。序列特征分析表明,该序列具备金属硫蛋白的典型特征,是金属硫蛋白家族的成员。
关键词:  海湾扇贝  金属硫蛋白基因  EST  cDNA文库
DOI:
分类号:
基金项目:863国家高技术研究发展计划资助项目,2002AA626020号;国家自然科学基金资助项目,40276045号
附件
CLONING AND CHARACTERIZATION OF A METALLOTHIONEIN GENE IN BAY SCALLOP ARGOPECTEN IRRADIANS
LIU Wei-Qing,NI Duo-Jiao,SONG Lin-Sheng,WU Long-Tao,XU Wei,KONG Xiao-Yu
1.Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071;2.College of Fisheries, Ocean University of China, Qingdao, 266003
Abstract:
Metallothioneins (MTs) are low molecular weight, cysteine-rich, inducible metal-binding proteins found in a variety of organ isms. MTs have many important biological functions acted as a protective role against excess reactive heavy metal ions, free radical scavengers and reservoir of essential metals that can be donated to other metalloproteins. A partial sequence of the bay scallop Argopecten irradians metallothione in (named as AMiT) gene was identified from A. irradians cDNA library using expressed sequence tag method. A pair o f gene-specific primers was designed according to this sequence and the full-length of AMiT cDNA was obtained using rapid amplification of cDNA end technique. The full-length cDNA of AMiT was of 787bp including a 5' untranslated region (UTR) of 79bp, a 3' UTR of 270 bp and an open reading frame (ORF) of 438bp encoding a polypeptide of 145 amino acids. The predicted amino acid sequence of AMiT contained 40 cysteine residues organized in Cys-X(n)-Cys (n=1–3) motif as classically described for MTs. The contents of cysteine, glycine and phenylalanine in the AMiT amino acids sequence were 27.6%, 13.1% and 2.1% respectively while no histidine residue was found. The CKCXXXCXCX motif, a conserved feature for invertebrate and molluscan MT, was found in two regions of the AMiT. A specific pattern of mollusca MT C-x-C-x(3)-C-T-G-x(3)-C-x-C-x(3)-C-x-C-K located at the C-terminal. The result of sequence analysis indicated that AMiT was the member of metallothione in family.
Key words:  Argopecten irradians, Metallothionein gene, EST, cDNA library
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