Molecular cloning and functional analysis of polymeric immunoglobulin receptor gene in orange-spotted grouper (Epinephelus coioides)

被引:68
作者
Feng, Li-Na [1 ,2 ]
Lu, Dan-Qi [2 ]
Bei, Jin-Xin [1 ,2 ]
Chen, Jie-Lin [1 ,2 ]
Liu, Yun [1 ,2 ]
Zhang, Yong [1 ,2 ]
Liu, Xiao-Chun [1 ,2 ]
Meng, Zi-Ning [1 ,2 ]
Wang, Lei [3 ]
Lin, Hao-Ran [1 ,2 ,4 ]
机构
[1] Sun Yat Sen Zhongshan Univ, Inst Aquat Econ Anim, State Key Lab Biocontrol, Coll Life Sci, Guangzhou 510275, Guangdong, Peoples R China
[2] Sun Yat Sen Zhongshan Univ, Inst Aquat Econ Anim, Guangdong Prov Key Lab Aquat Econ Anim, Coll Life Sci, Guangzhou 510275, Guangdong, Peoples R China
[3] Sun Yat Sen Zhongshan Univ, Dept Biochem, State Key Lab Biocontrol, Coll Life Sci, Guangzhou 510275, Guangdong, Peoples R China
[4] Hainan Univ, Coll Ocean, Haikou 570228, Peoples R China
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY | 2009年 / 154卷 / 03期
基金
中国博士后科学基金;
关键词
Polymeric immunoglobulin receptor; Fish mucosal immunity; Orange-spotted grouper (Epinephelus coioides); Immunoglobulins; Eukaryotic expression; FREE SECRETORY COMPONENT; IG RECEPTOR; J-CHAIN; EPITHELIAL TRANSPORT; MUCOSAL SURFACES; IMMUNE-RESPONSES; MACROPUS-EUGENII; TAMMAR WALLABY; CDNA CLONING; EXPRESSION;
D O I
10.1016/j.cbpb.2009.07.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As one of the most important mucosal effectors, polymeric immunoglobulin receptor (pIgR) mediates the transcytosis of polymeric immunoglobulins (pigs) to protect the organisms. In this study, a full-length cDNA of pIgR was isolated from orange-spotted grouper (Epinephelus coioides), and the sequence analysis of deduced protein revealed the presence of only two Ig-like domains (ILDs), and the absence of the conserved Ig-binding site and complementary determining region (CDR). The grouper pIgR mRNA was detected in almost all the peripheral tissues examined, especially the mucosal tissues by RT-PCR. Additionally, recombinant grouper pIgR was stably expressed in the COS-7 cell line and identified as a 40-kDa transmembrame receptor. Furthermore, the association of recombinant pIgR and purified grouper pIgM was demonstrated. Taken together, the present study provided strong evidence that grouper pIgR was produced as a transmembrane protein, and probably involved in the pIgM transport. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:282 / 289
页数:8
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