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对贾第虫克隆株GS/M-83-H7中参与抗原变异的基因(vsp基因)和包囊化相关基因(cwp 1基因)的正义和反义转录本进行定量评估。

Quantitative assessment of sense and antisense transcripts from genes involved in antigenic variation (vsp genes) and encystation (cwp 1 gene) of Giardia lamblia clone GS/M-83-H7.

作者信息

von Allmen N, Bienz M, Hemphill A, Müller N

机构信息

Institute of Parasitology, University of Berne, Länggass-Strasse 122, CH-3012 Berne, Switzerland.

出版信息

Parasitology. 2005 Apr;130(Pt 4):389-96. doi: 10.1017/s0031182004006742.

Abstract

Antigenic variation of the intestinal protozoan parasite Giardia lamblia is caused by an exchange of the parasite's variant surface protein (VSP) coat. Many investigations on antigenic variation were performed with G. lamblia clone GS/M-83-H7 which produces surface antigen VSP H7. To generate novel information on giardial vsp gene transcription, vsp RNA levels were assessed by quantitative reverse transcription-(RT)-PCR in both axenic VSP H7-type trophozoites and subvariants obtained after negative selection of GS/M-83-H7 trophozoites by treatment with a cytotoxic, VSP H7-specific monoclonal antibody. Our investigation was not restricted to the assessment of the sense vsp transcript levels but also included an approach aimed at the detection of complementary antisense vsp transcripts within the two trophozoite populations. We found that sense vsp H7 RNA predominated in VSP H7-type trophozoites while sense RNA from only one (vsp IVg) of 8 subvariant vsp genes totally analysed predominated in subvariant-type trophozoites. Interestingly, the two trophozoite populations exhibited a similar relative distribution regarding the vsp H7 and vsp IVg antisense RNA molecules. An analogous sense versus antisense RNA pattern was also observed when the transcripts of gene cwp 1 (encoding cyst wall protein 1) were investigated. Here, both types of RNA molecules only appeared after cwp 1 had been induced through in vitro encystation of the parasite. These findings for the first time demonstrated that giardial antisense RNA production did not occur in a constitutive manner but was directly linked to complementary sense RNA production after activation of the respective gene systems.

摘要

肠道原生动物寄生虫蓝氏贾第鞭毛虫的抗原变异是由寄生虫可变表面蛋白(VSP)外壳的交换引起的。许多关于抗原变异的研究是使用产生表面抗原VSP H7的蓝氏贾第鞭毛虫克隆GS/M-83-H7进行的。为了获得关于贾第虫vsp基因转录的新信息,通过定量逆转录 - (RT)-PCR评估了在无菌VSP H7型滋养体以及用细胞毒性的、VSP H7特异性单克隆抗体处理GS/M-83-H7滋养体进行阴性选择后获得的亚变体中的vsp RNA水平。我们的研究不仅限于评估有义vsp转录本水平,还包括一种旨在检测两个滋养体群体中互补反义vsp转录本的方法。我们发现有义vsp H7 RNA在VSP H7型滋养体中占主导,而在总共分析的8个亚变体vsp基因中只有一个(vsp IVg)的有义RNA在亚变体型滋养体中占主导。有趣的是,这两个滋养体群体在vsp H7和vsp IVg反义RNA分子方面表现出相似的相对分布。当研究基因cwp 1(编码囊壁蛋白1)的转录本时,也观察到了类似的有义与反义RNA模式。在这里,只有在寄生虫通过体外包囊诱导cwp 1后,这两种类型的RNA分子才会出现。这些发现首次证明,贾第虫反义RNA的产生不是组成性的,而是与相应基因系统激活后互补有义RNA的产生直接相关。

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