Cloning and expression of glucose regulated protein 78 (GRP78) in Fenneropenaeus chinensis
文献类型:期刊论文
作者 | Luan, Wei1,2; Li, Fuhua1; Zhang, Jiquan1; Wang, Bing1; Xiang, Jianhai1![]() |
刊名 | MOLECULAR BIOLOGY REPORTS
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出版日期 | 2009-02-01 |
卷号 | 36期号:2页码:289-298 |
关键词 | Glucose-regulated Protein 78 Fenneropenaeus Chinensis Heat Shock Wssv Challenge |
ISSN号 | 0301-4851 |
DOI | 10.1007/s11033-007-9178-z |
文献子类 | Article |
英文摘要 | GRP78 (78 kDa glucose-regulated protein), also known as BiP (immunoglobulin heavy-chain-binding protein), is an essential regulator of endoplasmic reticulum (ER) homeostasis because of its multiple functions in protein folding, ER calcium binding, and controlling of the activation of transmembrane ER stress sensors. In this report, we cloned the full length cDNA of GRP78 (FcGRP78) from Chinese shrimp Fenneropenaeus chinensis. This cDNA revealed a 2,325 bp with 1,968 bp open reading frame encoding 655 amino acids. This is the first reported GRP78 gene in Crustacea. The deduced amino acid sequence of FcGRP78 shared high identity with previously reported insect GRP78s: 86, 87 and 85% identity with GRP78s of Drosophila melanogaster, Aedes aegypti and Bombyx mori, respectively. Northern blot analysis shows that FcGRP78 is ubiquitously expressed in tissues of shrimp. Heat shock at 35A degrees C significantly enhanced the expression of FcGRP78 at the first hour, reached the maximum at 4 h post heat shock, dropped after that and resumed to the normal level until 48 h of post recovery at 25A degrees C. Additionally, differential expression of FcGRP78 was detected in haemocytes, hepatopancreas and lymphoid organ when shrimp were challenged by white spot syndrome virus (WSSV). We inferred that FcGRP78 may play important roles in chaperoning, protein folding and immune function of shrimp.; GRP78 (78 kDa glucose-regulated protein), also known as BiP (immunoglobulin heavy-chain-binding protein), is an essential regulator of endoplasmic reticulum (ER) homeostasis because of its multiple functions in protein folding, ER calcium binding, and controlling of the activation of transmembrane ER stress sensors. In this report, we cloned the full length cDNA of GRP78 (FcGRP78) from Chinese shrimp Fenneropenaeus chinensis. This cDNA revealed a 2,325 bp with 1,968 bp open reading frame encoding 655 amino acids. This is the first reported GRP78 gene in Crustacea. The deduced amino acid sequence of FcGRP78 shared high identity with previously reported insect GRP78s: 86, 87 and 85% identity with GRP78s of Drosophila melanogaster, Aedes aegypti and Bombyx mori, respectively. Northern blot analysis shows that FcGRP78 is ubiquitously expressed in tissues of shrimp. Heat shock at 35A degrees C significantly enhanced the expression of FcGRP78 at the first hour, reached the maximum at 4 h post heat shock, dropped after that and resumed to the normal level until 48 h of post recovery at 25A degrees C. Additionally, differential expression of FcGRP78 was detected in haemocytes, hepatopancreas and lymphoid organ when shrimp were challenged by white spot syndrome virus (WSSV). We inferred that FcGRP78 may play important roles in chaperoning, protein folding and immune function of shrimp. |
学科主题 | Biochemistry & Molecular Biology |
URL标识 | 查看原文 |
语种 | 英语 |
WOS记录号 | WOS:000262088300010 |
公开日期 | 2010-12-22 |
源URL | [http://ir.qdio.ac.cn/handle/337002/2985] ![]() |
专题 | 海洋研究所_实验海洋生物学重点实验室 |
作者单位 | 1.Chinese Acad Sci, Inst Oceanol, Qingdao 266071, Peoples R China 2.Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China |
推荐引用方式 GB/T 7714 | Luan, Wei,Li, Fuhua,Zhang, Jiquan,et al. Cloning and expression of glucose regulated protein 78 (GRP78) in Fenneropenaeus chinensis[J]. MOLECULAR BIOLOGY REPORTS,2009,36(2):289-298. |
APA | Luan, Wei,Li, Fuhua,Zhang, Jiquan,Wang, Bing,&Xiang, Jianhai.(2009).Cloning and expression of glucose regulated protein 78 (GRP78) in Fenneropenaeus chinensis.MOLECULAR BIOLOGY REPORTS,36(2),289-298. |
MLA | Luan, Wei,et al."Cloning and expression of glucose regulated protein 78 (GRP78) in Fenneropenaeus chinensis".MOLECULAR BIOLOGY REPORTS 36.2(2009):289-298. |
入库方式: OAI收割
来源:海洋研究所
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