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从中国明对虾(Fenneropenaeus chinensis)中克隆和表征 Rap GTPase。

Cloning and characterization of Rap GTPase from the Chinese white shrimp Fenneropenaeus chinensis.

机构信息

Institute of Life Sciences, Jiangsu University, Zhenjiang, Jiangsu, China.

出版信息

Dev Comp Immunol. 2012 Jan;36(1):247-52. doi: 10.1016/j.dci.2011.07.004. Epub 2011 Jul 27.

DOI:10.1016/j.dci.2011.07.004
PMID:21801745
Abstract

Ras-related protein Rap GTPase has been implicated in cell adhesion, cell proliferation, and cell junction formation. The first shrimp Rap cDNA (FcRap) was recently identified from the Chinese white shrimp Fenneropenaeus chinensis. The full length of FcRap is 1013 bp, with a 561 bp open reading frame that encodes a 186 amino acid protein. FcRap has a calculated molecular mass of 20.90 kDa and pI of 6.37. Phylogenetic analysis shows that FcRap and other Rap proteins are clustered into one group. Results from the quantitative real-time polymerase chain reaction show that FcRap could be detected mainly in the hemocytes, hepatopancreas, stomach, and gills, whereas a relatively lower expression level could be detected in the heart and intestines. FcRap in the hemocytes was upregulated 2h post Vibrio challenge, and it was upregulated 2h post white spot syndrome virus (WSSV) challenge, and peaked at 6h before it declined at 12h. No variation in the FcRap transcript was observed in the gills under the Vibrio challenge, but it was initially downregulated 2h post WSSV challenge, and then it was upregulated and peaked at 6h before it was eventually went down at 12h. The rFcRap protein was successfully expressed in Escherichia coli BL21DE3. The pull-down analysis showed that rFcRap protein could interact with VP28, an envelope protein of WSSV. The probable roles of Rap GTPase in shrimp innate immunity are presented for the first time.

摘要

Ras 相关蛋白 Rap GTP 酶参与细胞黏附、细胞增殖和细胞连接形成。最近从中国对虾(Fenneropenaeus chinensis)中鉴定出第一个虾 Rap cDNA(FcRap)。FcRap 的全长为 1013bp,具有 561bp 的开放阅读框,编码 186 个氨基酸的蛋白质。FcRap 的计算分子量为 20.90kDa,等电点为 6.37。系统发育分析表明,FcRap 和其他 Rap 蛋白聚类为一组。实时定量聚合酶链反应的结果表明,FcRap 主要在血细胞、肝胰腺、胃和鳃中检测到,而在心脏和肠道中检测到相对较低的表达水平。在受到弧菌刺激后 2 小时,血细胞中的 FcRap 上调,在受到白斑综合征病毒(WSSV)刺激后 2 小时上调,并在 6 小时达到峰值,然后在 12 小时下降。在受到弧菌刺激时,鳃中的 FcRap 转录物没有变化,但在受到 WSSV 刺激后 2 小时最初下调,然后上调并在 6 小时达到峰值,然后在 12 小时最终下降。rFcRap 蛋白在大肠杆菌 BL21DE3 中成功表达。下拉分析表明,rFcRap 蛋白可以与 WSSV 的包膜蛋白 VP28 相互作用。首次提出了 Rap GTP 酶在虾先天免疫中的可能作用。

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