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疫苗靶标氨基酸肽酶 H11 的基因结构和启动子区域,该靶标来源于反刍动物吸血线虫寄生虫旋毛虫(Haemonchus contortus)。

The gene structure and promoter region of the vaccine target aminopeptidase H11 from the blood-sucking nematode parasite of ruminants, Haemonchus contortus.

机构信息

Key Laboratory of Animal Epidemic Etiology & Immunological Prevention of Ministry of Agriculture, Institution of Preventive Veterinary Medicine, Zhejiang University, Hangzhou 310029, China.

出版信息

Funct Integr Genomics. 2010 Nov;10(4):589-601. doi: 10.1007/s10142-010-0172-5. Epub 2010 May 1.

Abstract

Aminopeptidase H11, an integral membrane glycoprotein present only in the gut of Haemonchus contortus, could provide substantial protection as shown by 90% reduction in fecal egg counts, while its recombinant version expressed in E. coli induced little. To investigate the characteristics further, we amplified mRNA of H11 gene via reverse transcriptase polymerase chain reaction, followed by isolation of its 1,517-bp 5'-flanking region and determination of its genomic organization. The H11 gene contained 25 exons separated by 24 introns and spans 14,959 bp of genomic DNA. Analysis of the 1,517 bp 5'-flanking region of the H11 gene revealed a putative "TATA-less" promoter. Partial sequences of the last exon and its 3'-UTR of H11 isoform H11-4 were also identified upstream to the H11 gene with the same transcription orientation. The 1,517-bp 5'-flanking region and part of the first exon of the H11 gene were subcloned into the vector upstream of green fluorescence protein reporter gene and microinjected into the gonads of Caenorhabditis elegans. The transformed animals exhibited fluorescence in the distal intestine in the L4 larvae stage and adult worms. This study characterized gene structure of aminopeptidase H11, demonstrated different transcriptional pattern of its promoter region between free-living and blood-sucking nematode species, and highlights the utility of C. elegans as a heterologous system to study the biology roles of H11 isoforms.

摘要

Aminopeptidase H11 是一种完整的膜糖蛋白,仅存在于捻转血矛线虫的肠道中,如粪便虫卵计数减少 90%所示,它能提供实质性的保护,而其在大肠杆菌中表达的重组版本则诱导作用较小。为了进一步研究其特性,我们通过逆转录聚合酶链反应扩增 H11 基因的 mRNA,然后分离其 1517bp 的 5'-侧翼区,并确定其基因组结构。H11 基因包含 25 个外显子,由 24 个内含子隔开,跨越 14959bp 的基因组 DNA。H11 基因的 1517bp 5'-侧翼区分析显示出一个推定的“无 TATA”启动子。H11 同工型 H11-4 的最后一个外显子及其 3'-UTR 的部分序列也在前 H11 基因上游被鉴定出来,转录方向相同。H11 基因的 1517bp 5'-侧翼区和第一外显子的部分序列被亚克隆到绿色荧光蛋白报告基因载体的上游,并微注射到秀丽隐杆线虫的性腺中。转化后的动物在 L4 幼虫阶段和成虫阶段的远端肠道中表现出荧光。本研究对氨基肽酶 H11 的基因结构进行了表征,证明了自由生活和吸血线虫物种之间其启动子区域的转录模式不同,并强调了秀丽隐杆线虫作为研究 H11 同工型生物学作用的异源系统的实用性。

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