脊尾白对虾含c型凝集素串联苏氨酸(Thr-Lec)的鉴定与功能分析

Huang Xin , Li Guanjie , Liu Beixiang , Zhou Chengxiang , Wang Hongyu , Qin Wei , Jiang Zuosheng , Wan Xihe , Ren Qian
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引用次数: 1

摘要

c型凝集素(C-type lecectin, ctl)作为一种重要的模式识别受体(pattern-recognition receptor, PRR),在先天免疫中识别微生物、对抗病原微生物等方面发挥着重要作用。在本研究中,我们从外皮emon carinicauda中鉴定出两个串联的含苏氨酸的ctl (EcThr-LecA和EcThr-LecB)。EcThr-LecA和EcThr-LecB cDNA全长分别为1521和1518 bp,其中开放阅读框长度分别为1251和1242 bp,分别编码含有412和413个氨基酸的蛋白。EcThr-LecA的基因组结构包括10个外显子和9个内含子,内含子6和内含子7的序列是可变的。EcThr-LecB中内含子2的核苷酸序列具有特异性,与EcThr-LecA不同。EcThr-LecA和EcThr-LecB蛋白具有一个信号肽、两个保守的碳水化合物识别结构域(CRD)和串联苏氨酸区域。在副溶血性弧菌和白斑综合征病毒(WSSV)侵袭后,EcThr-LecA和EcThr-LecB在肠道中的表达水平显著上调。采用RNA干扰(RNAi)技术探讨EcThr-LecB沉默对抗脂多糖因子(ALF)、硬壳蛋白(CRU)、溶菌酶(LYSO) mRNA表达的影响。敲低EcThr-LecB可显著下调EcALF2、EcCRU1、EcCRU3、EcCRU4、EcLYSO1、EcLYSO2、EcLYSO3和EcLYSO4等8种抗菌肽的表达,而对EcALF1、EcALF3、EcCRU2和EcLYSO5的转录无影响。重组EcThr-LecB的两个CRD结构域和串联苏氨酸区域(RLecB)在体外可以结合多种细菌、脂多糖和肽聚糖。此外,RLecB还能在体内加速副溶血性弧菌的清除。目前的数据表明,新发现的含有CTLs的串联苏氨酸可能作为PRR参与对病原体的先天免疫防御,通过对非自身的识别、amp的调节和对入侵者的清除。
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Characterization and functional analysis of tandem threonine containing C-type lectin (Thr-Lec) from the ridgetail white prawn Exopalaemon carinicauda

As an important pattern-recognition receptor (PRR), C-type lectins (CTLs) play significant roles in recognizing microbes and battle against pathogenic microorganism in innate immunity. In this study, two tandem threonine containing CTLs (designated as EcThr-LecA and EcThr-LecB) were identified from Exopalaemon carinicauda. The full-length cDNA of EcThr-LecA and EcThr-LecB consisted of 1521 and 1518 bp with 1251 and 1242 bp open reading frame encoding a protein with 412 and 413 amino acids, respectively. The genome structure of EcThr-LecA included 10 exons and 9 introns, and the sequences of intron6 and intron7 were variable. The nucleotide sequence of intron2 in EcThr-LecB was specific and different with that of EcThr-LecA. EcThr-LecA and EcThr-LecB proteins were predicted to have a signal peptide, two conserved carbohydrate recognition domain (CRD), and tandem threonine region. The expression levels of EcThr-LecA and EcThr-LecB in the intestine were significantly up-regulated after Vibrio parahaemolyticus and white spot syndrome virus (WSSV) challenge. RNA interference (RNAi) was used to explore the effects of EcThr-LecB silencing on the mRNA expression of anti-lipopolysaccharide factor (ALF), crustin (CRU), and lysozyme (LYSO). Knock down of EcThr-LecB could evidently down-regulate the expression of eight different antibacterial peptides (AMPs), including EcALF2, EcCRU1, EcCRU3, EcCRU4, EcLYSO1, EcLYSO2, EcLYSO3, and EcLYSO4, whereas make no effect on the transcription of EcALF1, EcALF3, EcCRU2, and EcLYSO5. The recombinant two CRD domains and tandem threonine region (RLecB) of EcThr-LecB could bind diverse bacteria, lipopolysaccharide, and peptidoglycans in vitro. In addition, RLecB could accelerate the clearance of V. parahaemolyticus in vivo. The present data indicated that new-found tandem threonine containing CTLs in E. carinicauda may act as PRR to participate in the innate immune defense against pathogens by the recognition of non-self, regulation of AMPs, and clearance of invaders.

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