Molecular characterization, expression and function analysis of a five-domain Kazal-type serine proteinase inhibitor from pearl oyster Pinctada fucata

文献类型: 外文期刊

第一作者: Zhang, Dianchang

作者: Zhang, Dianchang;Ma, Jianjun;Jiang, Shigui

作者机构:

关键词: Pinctada fucata;Serine proteinase inhibitor;Microbial challenge;Quantitative real-time PCR;Inhibitory activity

期刊名称:FISH & SHELLFISH IMMUNOLOGY ( 影响因子:4.581; 五年影响因子:4.851 )

ISSN: 1050-4648

年卷期: 2014 年 37 卷 1 期

页码:

收录情况: SCI

摘要: Serine proteinase inhibitors represent an expanding superfamily of endogenous inhibitors that are regulate proteolytic events and involved in a variety of physiological and immunological processes. A five-domain Kazal-type serine proteinase inhibitor (poKSPI) was identified and characterized from pearl oyster Pinctada fucata based on expressed sequence tag (EST) analysis. The full-length cDNA was 737 bp with an open reading frame (ORF) 660 bp encoding a 219 amino acid protein a theoretical molecular weight (Mw) of 23.3 kDa and an isoelectric point (pI) of 8.40. A putative signal peptide of 19 amino acid residues and five tandem Kazal domains were identified. Four of the Kazal domains had the highly conserved motif sequences with six cysteine residues responsible for the formation of disulfide bridges. The deduced amino acid sequence of the poKSPI shared high homology with KSPIs from Hirudo medicinalis. The poKSPI mRNA could be detected in all examined tissues, the expression level of the poKSPI mRNA was the highest in mantle and gonad, while the lowest in haemocyte and intestine. After LPS challenge, the expression level of the poKSPI mRNA in digestive gland was significantly up-regulated at 4 h post-challenge and reached the peak at 12 h post-challenge, which was 4.23-fold higher than control group; the expression level of the poKSPI mRNA in gill was also significantly up-regulated at 8 and 12 h post-challenge, which were 4.48 and 2.26-fold higher than control group. After Vibrio alginolyticus challenge, the expression levels of the poKSPI mRNA in digestive gland were significantly up-regulated at 8, 12, 48 and 72 h post-challenge, which were 1.70, 1.79, 3.89 and 5.69-fold higher than control group, respectively; the expression level of the poKSPI mRNA in gill was significantly up-regulated at 24 h post-challenge, which was 5.30-fold higher than control group. The recombinant poKSPI protein could inhibit chymotrypsin and trypsin activities in dose-dependent manner, when the ratios of rpoKSPI to chymotrypsin and trypsin were 36:1 and 72:1, respectively, the proteinase activities of chymotrypsin and trypsin could be almost completely inhibited, but the rpoKSPI could not inhibit subtilisin. (C) 2013 Published by Elsevier Ltd.

分类号:

  • 相关文献

[1]Synthesis and Insecticidal Activity of Novel Carbamate Derivatives as Potential Dual-Binding Site Acetylcholinesterase Inhibitors. Ma, Hong-Ju,Xie, Ru-Liang,Zhao, Qian-Fei,Mei, Xiang-Dong,Ning, Jun,Ma, Hong-Ju.

[2]Functional characterization of a cystatin from the tick Rhipicephalus haemaphysaloides. Wang, Yujian,Zhou, Yongzhi,Gong, Haiyan,Cao, Jie,Zhang, Houshuang,Zhou, Jinlin,Wang, Yujian,Li, Xiangrui,Zhou, Jinlin. 2015

[3]Cholinesterase and Human Lung Cancer Cells (A-549) Inhibitory Activity of the Cassava Peel of Euphorbiaceae in Vitro. Chen, Xiao-Ming,Zhang, Zhi-Jun,Li, Shu-Fang,Liu, Ai-Lin,Lv, Fei-Jie. 2016

[4]Design of novel carbamate acetylcholinesterase inhibitors based on the multiple binding sites of acetylcholinesterase. Mei, Xiangdong,Yuan, Huizhu,Ning, Jun,Zhao, Qianfei.

[5]Cloning and sequencing of a lectin protein gene from the roots of Sophora flavescens. Ma, ZG,Yan, B,Huang, XQ,Wang, LX,Zeng, ZK. 2001

[6]Characterization of a secreted cystatin from the tick Rhipicephalus haemaphysaloides. Wang, Yujian,Yu, Xinmao,Cao, Jie,Zhou, Yongzhi,Gong, Haiyan,Zhang, Houshuang,Zhou, Jinlin,Wang, Yujian,Li, Xiangrui.

[7]Molecular characterization and expression analysis of the I kappa B gene from pearl oyster Pinctada fucata. Xu, Xinping,Zhang, Dianchang,Jiang, Shigui,Qiu, Lihua,Su, Tianfeng,Wu, Kaichang,Li, Youning,Zhu, Caiyan,Zhang, Dianchang. 2009

[8]Common pearl oysters in China, Japan, and Australia are conspecific: evidence from ITS sequences and AFLP. Yu, Da Hui,Jia, Xiaoping,Chu, Ka Hou. 2006

[9]Molecular characterization and expression analysis of a putative LPS-induced TNF-alpha factor (LITAF) from pearl oyster Pinctada fucata. Zhang, Dianchang,Jiang, Jingjing,Jiang, Shigui,Ma, Jianjun,Su, Tianfeng,Qiu, Lihua,Zhu, Caiyan,Zhang, Dianchang,Jiang, Jingjing,Ma, Jianjun,Xu, Xinping,Xu, Xinping. 2009

[10]Identification of twenty novel polymorphic microsatellite DNA markers from transcripts of the pearl oyster Pinctada fucata using next-generation sequencing approach. Fan, Sigang,Wang, Jingxuan,Huang, Guiju,Liu, Baosuo,Yu, Dahui,Wang, Jingxuan. 2015

[11]Isolation and screening of microsatellite markers from the pearl oyster, Pinctada fucata using FIASCO method. Yu, Da-Hui,Qu, Ni-Ni,Huang, Gui-Ju. 2015

[12]Molecular characterization and expression analysis of lipopolysaccharide and beta-1,3-glucan-binding protein (LGBP) from pearl oyster Pinctada fucata. Zhang, Dianchang,Ma, Jianjun,Jiang, Jingjing,Qiu, Lihua,Zhu, Caiyan,Su, Tianfeng,Li, Youning,Wu, Kaichang,Jiang, Shigui,Ma, Jianjun. 2010

[13]Molecular characterization and expression analysis of interferon-gamma-inducible lysosomal thiol reductase (GILT) gene from pearl oyster Pinctada fucata. Zhang, Dianchang,Pan, Dequan,Cui, Shuge,Su, Tianfeng,Qiu, Lihua,Zhu, Caiyan,Jiang, Shigui,Pan, Dequan,Cui, Shuge. 2010

[14]cDNA cloning and mRNA expression of a tandem-repeat galectin (PoGal2) from the pearl oyster, Pinctada fucata. Zhang, D. C.,Hu, Y. T.,Guo, H. Y.,Cui, S. G.,Su, T. F.,Jiang, S. G.,Hu, Y. T.,Guo, H. Y.,Jiang, S. G.. 2011

[15]A macrophage migration inhibitory factor like oxidoreductase from pearl oyster Pinctada fucata involved in innate immune responses. Cui, Shuge,Zhang, Dianchang,Jiang, Shigui,Hu, Yuting,Guo, Huayang,Chen, Mingqiang,Su, Tanfeng,Zhu, Caiyan,Cui, Shuge,Pu, Hanlin. 2011

[16]Transcriptome analysis of the immune reaction of the pearl oyster Pinctada fucata to xenograft from Pinctada maxima. Wei, Jinfen,Yu, Dahui,Wei, Jinfen,Fan, Sigang,Liu, Baosuo,Zhang, Bo,Su, Jiaqi,Wei, Jinfen.

[17]Identification and Differential Expression of Biomineralization Genes in the Mantle of Pearl Oyster Pinctada fucata. Li, Haimei,Yu, Dahui,Li, Haimei,Yu, Dahui,Li, Haimei,Zhang, Bo,Fan, Sigang,Liu, Baosuo,Su, Jiaqi,Yu, Dahui,Yu, Dahui,Yu, Dahui.

[18]A multidomain galectin involved in innate immune response of pearl oyster Pinctada fucata. Zhang, Dianchang,Jiang, Shigui,Hu, Yuting,Cui, Shuge,Guo, Huayang,Wu, Kaichang,Li, Youning,Su, Tianfeng,Hu, Yuting,Guo, Huayang,Cui, Shuge.

[19]A preliminary study for identification of candidate AFLP markers under artificial selection for shell color in pearl oyster Pinctada fucata. Zou, Keshu,Zhang, Dianchang,Guo, Huayang,Zhu, Caiyan,Li, Min,Jiang, Shigui,Zou, Keshu,Zhang, Dianchang,Li, Min,Jiang, Shigui.

[20]Low genetic differentiation among widely separated populations of the pearl oyster Pinctada fucata as revealed by AFLP. Yu, DH,Chu, KH.

作者其他论文 更多>>