Institutional Repository of Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences
Molecular cloning, characterization and mRNA expression of peroxiredoxin in Zhikong scallop Chlamys farreri | |
Cong, Ming1,2; Ni, Duojiao1,2; Song, Linsheng1; Wang, Lingling1; Zhao, Jianmin1; Qiu, Limei1; Li, Ling1,2 | |
2009-07-01 | |
发表期刊 | MOLECULAR BIOLOGY REPORTS |
ISSN | 0301-4851 |
卷号 | 36期号:6页码:1451-1459 |
文章类型 | Article |
摘要 | Peroxiredoxin V (PRX V) is known as an atypical 2-cysteine peroxiredoxin that protects the organisms against various oxidative stresses and functions in signal transduction. The cDNA of a PRX V gene (designated as CfPRX) was cloned from scallop Chlamys farreri. The full-length sequence of CfPRX cDNA was of 2,179 bp with a 564 bp open reading frame encoding a peptide of 187 amino acids. Sequence comparison showed that CfPRX shared higher identities with PRX Vs than that with other isoforms of PRX, indicating CfPRX was a member of the PRX V family. Fluorescent real-time quantitative PCR analysis revealed the presence of CfPRX transcripts in gill filaments, adductor muscle, heart, gonad, kidney and hemocytes, and the stimulation of Listonella anguillarum significantly (P < 0.01) enhanced the mRNA expression of CfPRX in hemocyte. These results indicated that CfPRX was a constitutive and inducible acute-phase protein which was involved in the immune resistance to L. anguillarum stimulation.; Peroxiredoxin V (PRX V) is known as an atypical 2-cysteine peroxiredoxin that protects the organisms against various oxidative stresses and functions in signal transduction. The cDNA of a PRX V gene (designated as CfPRX) was cloned from scallop Chlamys farreri. The full-length sequence of CfPRX cDNA was of 2,179 bp with a 564 bp open reading frame encoding a peptide of 187 amino acids. Sequence comparison showed that CfPRX shared higher identities with PRX Vs than that with other isoforms of PRX, indicating CfPRX was a member of the PRX V family. Fluorescent real-time quantitative PCR analysis revealed the presence of CfPRX transcripts in gill filaments, adductor muscle, heart, gonad, kidney and hemocytes, and the stimulation of Listonella anguillarum significantly (P < 0.01) enhanced the mRNA expression of CfPRX in hemocyte. These results indicated that CfPRX was a constitutive and inducible acute-phase protein which was involved in the immune resistance to L. anguillarum stimulation. |
关键词 | Chlamys Farreri Fluorescent Real-time Quantitative Pcr Immune Response Listonella Anguillarum Peroxiredoxin |
学科领域 | Biochemistry & Molecular Biology |
DOI | 10.1007/s11033-008-9335-z |
URL | 查看原文 |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000266454500034 |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | http://ir.qdio.ac.cn/handle/337002/2886 |
专题 | 实验海洋生物学重点实验室 |
作者单位 | 1.Chinese Acad Sci, Inst Oceanol, Qingdao 266071, Shandong, Peoples R China 2.Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China |
第一作者单位 | 中国科学院海洋研究所 |
推荐引用方式 GB/T 7714 | Cong, Ming,Ni, Duojiao,Song, Linsheng,et al. Molecular cloning, characterization and mRNA expression of peroxiredoxin in Zhikong scallop Chlamys farreri[J]. MOLECULAR BIOLOGY REPORTS,2009,36(6):1451-1459. |
APA | Cong, Ming.,Ni, Duojiao.,Song, Linsheng.,Wang, Lingling.,Zhao, Jianmin.,...&Li, Ling.(2009).Molecular cloning, characterization and mRNA expression of peroxiredoxin in Zhikong scallop Chlamys farreri.MOLECULAR BIOLOGY REPORTS,36(6),1451-1459. |
MLA | Cong, Ming,et al."Molecular cloning, characterization and mRNA expression of peroxiredoxin in Zhikong scallop Chlamys farreri".MOLECULAR BIOLOGY REPORTS 36.6(2009):1451-1459. |
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