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外壳中的裂缝——聚焦人类寄生虫曼氏血吸虫的蛋壳形成

Cracks in the shell--zooming in on eggshell formation in the human parasite Schistosoma mansoni.

作者信息

Ebersberger Ingo, Knobloch Jürgen, Kunz Werner

机构信息

Institute for Bioinformatics, Heinrich Heine University, 40225 Düsseldorf, Germany.

出版信息

Dev Genes Evol. 2005 May;215(5):261-7. doi: 10.1007/s00427-005-0467-z. Epub 2005 Mar 4.

DOI:10.1007/s00427-005-0467-z
PMID:15747129
Abstract

Schistosomiasis, currently the second most common parasitic disease of humans in tropical regions is caused by the eggs of trematode worms of the genus Schistosoma. Understanding egg formation and specifically the synthesis of the eggshell comprises, consequently, a promising starting point to cure and prevent the disease. To shed light on the genetics of the latter process, we analysed the three known S. mansoni eggshell proteins P14, P19 and P48 against the background of the species' inferred proteome and of eggshell proteins identified in other trematode species. Our results suggest that eggshell formation in Schistosoma involves a multitude of different proteins organised in currently three distinct protein families (P14, P48 and P34 eggshell protein family). The first two families are of simple structure. Their respective members share a substantial degree of sequence similarity and are, to date, observed only in the genus Schistosoma. In contrast, the P34 family of eggshell proteins is complex. Its in part highly diverged members share only a conserved motif of 67-aa length on average and are detected in various trematode species. The resulting widespread occurrence of this protein motif suggests an important role during eggshell formation in trematodes. Screening more than 7,000 putative proteins of S. mansoni, we could identify six new members of the P34 protein family that are likely to be involved in eggshell formation in this species.

摘要

血吸虫病是目前热带地区人类第二常见的寄生虫病,由血吸虫属吸虫的虫卵引起。因此,了解虫卵形成过程,特别是卵壳的合成,是治愈和预防该疾病的一个有前景的切入点。为了阐明这一过程的遗传学,我们在曼氏血吸虫推断的蛋白质组以及在其他吸虫物种中鉴定出的卵壳蛋白的背景下,分析了三种已知的曼氏血吸虫卵壳蛋白P14、P19和P48。我们的结果表明,血吸虫的卵壳形成涉及众多不同的蛋白质,目前这些蛋白质组织成三个不同的蛋白质家族(P14、P48和P34卵壳蛋白家族)。前两个家族结构简单。它们各自的成员具有高度的序列相似性,并且迄今为止仅在血吸虫属中观察到。相比之下,P34卵壳蛋白家族则较为复杂。其部分高度分化的成员平均仅共享一个长度为67个氨基酸的保守基序,并且在各种吸虫物种中都能检测到。这种蛋白质基序的广泛存在表明它在吸虫卵壳形成过程中起着重要作用。通过筛选曼氏血吸虫的7000多种推定蛋白,我们鉴定出了P34蛋白家族的六个新成员,它们可能参与了该物种的卵壳形成。

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