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多房棘球绦虫中Ras和Raf同源物的分子克隆与特性分析

Molecular cloning and characterization of Ras- and Raf-homologues from the fox-tapeworm Echinococcus multilocularis.

作者信息

Spiliotis Markus, Tappe Dennis, Brückner Stefan, Mösch Hans-Ulrich, Brehm Klaus

机构信息

Institute of Hygiene and Microbiology, Julius-Maximilians University, D-97080 Würzburg, Germany.

出版信息

Mol Biochem Parasitol. 2005 Feb;139(2):225-37. doi: 10.1016/j.molbiopara.2004.11.013.

Abstract

To better understand growth regulation in the human parasitic cestode Echinococcus multilocularis, we have cloned and characterized the parasite's orthologues of the key regulatory factors Ras and Raf. Using a degenerative PCR approach a gene, emras, was identified whose gene product, EmRas, showed high homology (79% identical residues) to human Ras and contained all amino acid residues which are characteristic for this subfamily of small GTPases at the corresponding positions. Recombinantly expressed EmRas bound GTP and was farnesylated, but not geranyl-geranylated, by Echinococcus lysate in an in vitro prenylation assay. Furthermore, upon expression in yeast, emras was able to functionally complement the Saccharomyces orthologue RAS2 in an invasive growth assay. In Western blot analyses using an anti-EmRas antibody, the Echinococcus factor could be detected in lysates of the larval stages metacestode and protoscolex. By immune-histochemistry, EmRas was shown to localize to the germinal layer of the metacestode and to tegumental structures of the protoscolex, particularly around the rostellum and the sucker regions. In addition, we fully characterized the gene emraf whose product, EmRaf, displayed considerable homology to mammalian Raf-kinases and orthologous factors from Drosophila and Caenorhabditis elegans. emraf was co-expressed with emras in the larval stages metacestode and protoscolex during in vitro cultivation and during an infection of the intermediate host as assessed by RT-PCR experiments. The emraf gene was composed of nine exons and eight introns and shared four highly conserved exon-intron boundaries with the human gene encoding Raf-1, suggesting that both genes derived from a common evolutionary ancestor. Southern blot hybridizations demonstrated that emraf is a single copy gene. Using the yeast two-hybrid system, EmRaf was shown to interact with EmRas, but not with EmRal, a previously characterized orthologue of mammalian Ral GTPases. This is the first characterization of a Ras orthologue from a cestode and the first report on a Raf-like kinase from a platyhelminth. The data presented herein will form a solid basis for further investigations on Echinococcus signaling systems that are involved in growth control and development of the parasite.

摘要

为了更好地理解人体寄生绦虫多房棘球绦虫的生长调控机制,我们克隆并鉴定了该寄生虫关键调控因子Ras和Raf的直系同源物。采用简并PCR方法鉴定出一个基因emras,其基因产物EmRas与人类Ras具有高度同源性(79%的相同残基),并且在相应位置包含了小GTP酶亚家族的所有特征性氨基酸残基。在体外异戊二烯化试验中,重组表达的EmRas能结合GTP,并被多房棘球绦虫裂解物法尼基化,但未被香叶基香叶基化。此外,在酵母中表达时,emras在侵袭性生长试验中能够在功能上互补酿酒酵母的直系同源物RAS2。在使用抗EmRas抗体的蛋白质印迹分析中,可在幼虫期的囊尾蚴和原头蚴裂解物中检测到该多房棘球绦虫因子。通过免疫组织化学方法,发现EmRas定位于囊尾蚴的生发层和原头蚴的皮层结构,特别是在顶突和吸盘区域周围。此外,我们对基因emraf进行了全面鉴定,其产物EmRaf与哺乳动物Raf激酶以及果蝇和秀丽隐杆线虫的直系同源因子具有显著同源性。通过逆转录-聚合酶链反应(RT-PCR)实验评估,在体外培养期间以及中间宿主感染期间,emraf与emras在幼虫期的囊尾蚴和原头蚴中共同表达。emraf基因由九个外显子和八个内含子组成,与编码Raf-1的人类基因共有四个高度保守的外显子-内含子边界,这表明这两个基因来源于共同的进化祖先。Southern印迹杂交表明emraf是单拷贝基因。利用酵母双杂交系统,发现EmRaf与EmRas相互作用,但不与EmRal相互作用,EmRal是先前鉴定的哺乳动物Ral GTP酶的直系同源物。这是首次对绦虫的Ras直系同源物进行鉴定,也是首次报道来自扁形动物的Raf样激酶。本文提供的数据将为进一步研究参与寄生虫生长控制和发育的多房棘球绦虫信号系统奠定坚实基础。

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