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长角血蜱微小牛蜱Bm86同源物的分子特征分析

Molecular characterization of Rhipicephalus (Boophilus) microplus Bm86 homologue from Haemaphysalis longicornis ticks.

作者信息

Liao Min, Zhou Jinlin, Hatta Takeshi, Umemiya Rika, Miyoshi Takeharu, Tsuji Naotoshi, Xuan Xuenan, Fujisaki Kozo

机构信息

National Research Center for Protozoan Diseases, Obihiro University of Agriculture and Veterinary Medicine, Inada-cho, Obihiro, Hokkaido 080-8555, Japan.

出版信息

Vet Parasitol. 2007 May 15;146(1-2):148-57. doi: 10.1016/j.vetpar.2007.01.015. Epub 2007 Mar 23.

Abstract

One sequence in the EST database of a midgut cDNA library prepared from semi-engorged female Haemaphysalis longicornis ticks has been found to be a homologue of the Bm86 gene of Rhipicephalus (Boophilus) microplus ticks. The full-length sequence containing a 1785 bp open reading fragment (ORF) was obtained and designated as the Hl86 gene. The predicted amino acid sequence of the Hl86 gene shows a 37% identity to the Bm86 gene. Hl86 is predicted to be a GPI-anchored membrane-bound glycoprotein with a 19-amino acid signal sequence and a 22-amino acid hydrophobic region adjacent to the carboxyl terminus. The most important feature that Hl86 has in common with Bm86 is the repeated pattern of 6 cysteine residues forming epidermal growth factor (EGF)-like domains. RT-PCR analysis showed that Hl86 mRNA transcripts are expressed in all the life cycles of H. longicornis, and the expression was found in the midgut of the adult tick. The Hl86 was expressed in Escherichia coli as a gene10 fusion protein. Mouse anti-recombinant Hl86 serum recognized an 86 kDa protein band in the midgut lysate of semi-engorged ticks in Western blot analysis and showed a strong reaction on the luminal surface of midgut cells in an indirect immunofluorescent antibody test (IFAT). Silencing of the Hl86 gene by RNAi led to a significant reduction in the engorged tick body weight. This is the first report of cloning and characterization of the Bm86 homologue in different genera and species of ixodid and argasid ticks since Bm86 was first reported in 1989.

摘要

从半饱血的长角血蜱雌蜱制备的中肠cDNA文库的EST数据库中,发现一个序列是微小牛蜱Bm86基因的同源物。获得了包含1785 bp开放阅读框(ORF)的全长序列,并将其命名为Hl86基因。Hl86基因预测的氨基酸序列与Bm86基因有37%的同一性。Hl86预计是一种糖基磷脂酰肌醇(GPI)锚定的膜结合糖蛋白,具有19个氨基酸的信号序列和靠近羧基末端的22个氨基酸的疏水区域。Hl86与Bm86最重要的共同特征是6个半胱氨酸残基形成表皮生长因子(EGF)样结构域的重复模式。RT-PCR分析表明,Hl86 mRNA转录本在长角血蜱的所有生命周期中均有表达,且在成年蜱的中肠中也有表达。Hl86在大肠杆菌中作为基因10融合蛋白表达。在蛋白质印迹分析中,小鼠抗重组Hl86血清识别半饱血蜱中肠裂解物中的一条86 kDa蛋白条带,并且在间接免疫荧光抗体试验(IFAT)中对中肠细胞的腔表面显示出强烈反应。通过RNA干扰使Hl86基因沉默导致饱血蜱体重显著降低。这是自1989年首次报道Bm86以来,在硬蜱和软蜱不同属和种中克隆和鉴定Bm86同源物的首次报道。

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