Richter Sandy, Helm Conrad, Meunier Frederic A, Hering Lars, Campbell Lahcen I, Drukewitz Stephan H, Undheim Eivind A B, Jenner Ronald A, Schiavo Giampietro, Bleidorn Christoph
Institute of Biology - Molecular Evolution and Systematics of Animals, University of Leipzig, Talstraße 33, D-04103, Leipzig, Germany.
German Centre for Integrative Biodiversity Research (iDiv) Halle-Jena-Leipzig, Deutscher Platz 5e, D-04103, Leipzig, Germany.
BMC Evol Biol. 2017 Mar 4;17(1):64. doi: 10.1186/s12862-017-0904-4.
We present the first molecular characterization of glycerotoxin (GLTx), a potent neurotoxin found in the venom of the bloodworm Glycera tridactyla (Glyceridae, Annelida). Within the animal kingdom, GLTx shows a unique mode of action as it can specifically up-regulate the activity of Ca2.2 channels (N-type) in a reversible manner. The lack of sequence information has so far hampered a detailed understanding of its mode of action.
Our analyses reveal three ~3.8 kb GLTx full-length transcripts, show that GLTx represents a multigene family, and suggest it functions as a dimer. An integrative approach using transcriptomics, quantitative real-time PCR, in situ hybridization, and immunocytochemistry shows that GLTx is highly expressed exclusively in four pharyngeal lobes, a previously unrecognized part of the venom apparatus.
Our results overturn a century old textbook view on the glycerid venom system, suggesting that it is anatomically and functionally much more complex than previously thought. The herein presented GLTx sequence information constitutes an important step towards the establishment of GLTx as a versatile tool to understand the mechanism of synaptic function, as well as the mode of action of this novel neurotoxin.
我们首次对甘油毒素(GLTx)进行了分子特征分析,GLTx是在血虫三叉真蚓(甘油科,环节动物门)毒液中发现的一种强效神经毒素。在动物界中,GLTx显示出独特的作用方式,因为它可以以可逆方式特异性上调Ca2.2通道(N型)的活性。迄今为止,缺乏序列信息阻碍了对其作用方式的详细了解。
我们的分析揭示了三个约3.8 kb的GLTx全长转录本,表明GLTx代表一个多基因家族,并提示其作为二聚体发挥作用。使用转录组学、定量实时PCR、原位杂交和免疫细胞化学的综合方法表明,GLTx仅在四个咽叶中高度表达,咽叶是毒液器官中一个以前未被认识的部分。
我们的结果推翻了一个世纪以来教科书上关于甘油科毒液系统的观点,表明其在解剖学和功能上比以前认为的要复杂得多。本文提供的GLTx序列信息是朝着将GLTx确立为理解突触功能机制以及这种新型神经毒素作用方式的通用工具迈出的重要一步。