...
首页> 外文期刊>Immunogenetics >Characterization and expression of gamma-interferon-inducible lysosomal thiol reductase (GILT) gene in rainbow trout (Oncorhynchus mykiss) with implications for GILT in innate immune response
【24h】

Characterization and expression of gamma-interferon-inducible lysosomal thiol reductase (GILT) gene in rainbow trout (Oncorhynchus mykiss) with implications for GILT in innate immune response

机译:虹鳟(Oncorhynchus mykiss)γ-干扰素诱导溶酶体硫醇还原酶(镀锌)基因的表达及表达,在先天免疫应答中的粘附性中的影响

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The interferon-γ-inducible lysosomal thiol reductase (GILT) has been demonstrated to play an important role in the processing and presentation of MHC class II-restricted antigen (Ag) by catalyzing disulfide bond reduction. In this study, a rainbow trout cDNA (designated as rGILT) was cloned and identified from Oncorhynchus mykiss. The open reading frame of rGILT consists of 759 bases encoding a protein of 253 amino acids with an estimated molecular mass of 28.23 kDa and a theoretical isoelectric point of 4.94. The rGILT exhibited a characteristic GILT signature sequence CQHGX2ECX2NX 4C and CXXC motif. Phylogenetic analysis suggested that rGILT had been derived from a common ancestor with other GILT proteins. RT-PCR results showed that rGILT and rIFN-γ (rainbow trout IFN-γ) mRNA was expressed in a tissue-specific manner and obviously up-regulated in splenocytes and the cells from head kidney after induction with LPS. Recombinant rGILT fused with His6 tag was efficiently expressed in Escherichia coli BL21 (DE3) and purified by Ni-NTA affinity chromatography. Further study revealed that rGILT was capable of catalyzing the reduction of the interchain disulfide bonds from intact IgG. This study shows that rGILT may be involved in the immune response to bacteria challenge and maintain first line of innate immune defense at basal level in O. mykiss. It also provides the basis for investigating on the role of GILT using O. mykiss as an animal model for related studies.
机译:已经证明了干扰素-γ-诱导型溶酶体硫醇还原酶(镀锌)以通过催化二硫键还原在MHC II限制抗原(Ag)的加工和呈递中起重要作用。在这项研究中,克隆并鉴定了虹鳟鱼cDNA(指定为Rgilt)并鉴定于oncorhynchus mykiss。 RGILT的开放阅读框架由759个碱基组成,编码253个氨基酸的蛋白质,估计的分子量为28.23kDa和4.94的理论等电点。 RGILT表现出特征镀金签名序列CQHGX2ECX2NX 4C和CXXC基序。系统发育分析表明RGILT已从与其他镀层蛋白质中的共同祖先衍生出来。 RT-PCR结果表明,RGILT和RIFN-γ(彩虹鳟鱼IFN-γ)mRNA以组织特异性方式表达,并在脾细胞和LPS诱导后,在脾细胞和来自头肾的细胞中明显上调。与HIS6标签融合的重组RGILD在大肠杆菌BL21(DE3)中有效地表达,并通过Ni-NTA亲和层析纯化。进一步的研究表明,RGILT能够催化来自完整IgG的中间链硫键的还原。本研究表明,rgilt可以参与对细菌的免疫应答,并在米克西斯的基础上维持基础水平的第一线。它还提供了使用O. Mykiss作为相关研究的动物模型来研究镀金的作用的基础。

著录项

  • 来源
    《Immunogenetics》 |2013年第12期|共10页
  • 作者单位

    Jiangsu Province Key Laboratory for Molecular and Medical Biotechnology Life Sciences College;

    Jiangsu Province Key Laboratory for Molecular and Medical Biotechnology Life Sciences College;

    Jiangsu Province Key Laboratory for Molecular and Medical Biotechnology Life Sciences College;

    Jiangsu Province Key Laboratory for Molecular and Medical Biotechnology Life Sciences College;

    Jiangsu Province Key Laboratory for Molecular and Medical Biotechnology Life Sciences College;

    Jiangsu Province Key Laboratory for Molecular and Medical Biotechnology Life Sciences College;

    Jiangsu Province Key Laboratory for Molecular and Medical Biotechnology Life Sciences College;

    Jiangsu Province Key Laboratory for Molecular and Medical Biotechnology Life Sciences College;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医学免疫学;
  • 关键词

    Lipopolysaccharide (LPS); Oncorhynchus mykiss; Phylogenetic analysis; Real-time PCR; rGILT; Thiol reductase activity;

    机译:脂多糖(LPS);oncorhynchus mykiss;系统发育分析;实时PCR;rgilt;硫醇还原酶活性;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号