Krzysztof Kowalski, Paweł Marciniak, K Anne-Isola Nekaris, Leszek Rychlik
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Applying a proteomic approach coupled with Gene Ontology enrichment analysis, we identified 313 and 187 putative proteins in venom glands of N. fodiens and S. araneus, respectively. A search of the UniProt database revealed that most of the proteins found in both shrew species were involved in metabolic processes and stress response, while GO enrichment analysis revealed more stress-related proteins in the glands of S. araneus. Molecules that regulate molecule synthesis, cell cycles, and cell divisions are necessary to enable venom regeneration and ensure its effectiveness in predation and food hoarding. The presence of proteins involved in stress response may be the result of shrews' high metabolic rate and the costs of venom replenishment. Some proteins are likely to promote toxin spreading during envenomation and, due to their proteolytic action, reinforce venom toxicity. Finally, finding numerous proteins involved in immune response suggests a potential role of shrew venom gland secretions in protection against pathogens. These findings open up new perspectives for studying biological functions of molecules from shrew venom glands and extend our knowledge on the functioning of eulipotyphlan venom systems. 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引用次数: 0
摘要
毒液的产生在动物界中多次独立进化,但在哺乳动物中却很少见。毒鼩鼱在颌下唾液腺中分泌毒液,并利用毒液获取食物。迄今为止,只在鼩鼱毒液中发现了几种毒素,它们的作用方式还需要研究。与毒液产生和腺体功能有关的生物和分子过程也仍然未知。为了填补这一空白,我们研究了两种鼩鼱(Neomys fodiens和Sorex araneus)毒腺提取物中的蛋白质含量,并解读了它们的生物功能。通过蛋白质组学方法和基因本体富集分析,我们在 N. fodiens 和 S. araneus 的毒腺中分别发现了 313 和 187 个假定蛋白质。对 UniProt 数据库的检索显示,在这两种鼩鼱体内发现的大多数蛋白质都参与了新陈代谢过程和应激反应,而 GO 富集分析则显示在 S. araneus 的毒腺中发现了更多与应激反应有关的蛋白质。调控分子合成、细胞周期和细胞分裂的分子是毒液再生的必要条件,也是确保毒液在捕食和囤积食物过程中的有效性的必要条件。鼩鼱的新陈代谢率很高,毒液补充的成本也很高,因此可能存在涉及应激反应的蛋白质。有些蛋白质可能会在鼩鼱中毒时促进毒素扩散,并由于其蛋白质分解作用而加强毒液的毒性。最后,发现大量参与免疫反应的蛋白质表明,鼩鼱毒腺分泌物在抵御病原体方面具有潜在作用。这些发现为研究鼩鼱毒腺分子的生物功能开辟了新的视角,并扩展了我们对鼩鼱毒腺系统功能的认识。由于大多数现有的和推测的有毒哺乳动物都使用口腔毒液系统向目标物种注射毒液,因此本文介绍的方法为确认或发现有毒哺乳动物的新类群提供了一个很有希望的途径。
Proteins from shrews' venom glands play a role in gland functioning and venom production.
Venom production has evolved independently many times in the animal kingdom, although it is rare among mammals. Venomous shrews produce venom in their submandibular salivary glands and use it for food acquisition. Only a few toxins have been identified in shrew venoms thus far, and their modes of action require investigation. The biological and molecular processes relating to venom production and gland functioning also remain unknown. To address this gap, we investigated protein content in extracts from venom glands of two shrew species, Neomys fodiens and Sorex araneus, and interpreted their biological functions. Applying a proteomic approach coupled with Gene Ontology enrichment analysis, we identified 313 and 187 putative proteins in venom glands of N. fodiens and S. araneus, respectively. A search of the UniProt database revealed that most of the proteins found in both shrew species were involved in metabolic processes and stress response, while GO enrichment analysis revealed more stress-related proteins in the glands of S. araneus. Molecules that regulate molecule synthesis, cell cycles, and cell divisions are necessary to enable venom regeneration and ensure its effectiveness in predation and food hoarding. The presence of proteins involved in stress response may be the result of shrews' high metabolic rate and the costs of venom replenishment. Some proteins are likely to promote toxin spreading during envenomation and, due to their proteolytic action, reinforce venom toxicity. Finally, finding numerous proteins involved in immune response suggests a potential role of shrew venom gland secretions in protection against pathogens. These findings open up new perspectives for studying biological functions of molecules from shrew venom glands and extend our knowledge on the functioning of eulipotyphlan venom systems. Because the majority of existing and putative venomous mammals use oral venom systems to inject venom into target species, the methods presented here provide a promising avenue for confirming or discovering new taxa of venomous mammals.
Zoological LettersAgricultural and Biological Sciences-Animal Science and Zoology
CiteScore
3.60
自引率
0.00%
发文量
12
审稿时长
10 weeks
期刊介绍:
Zoological Letters is an open access journal that publishes new and important findings in the zoological sciences. As a sister journal to Zoological Science, Zoological Letters covers a wide range of basic fields of zoology, from taxonomy to bioinformatics. We also welcome submissions of paleontology reports as part of our effort to contribute to the development of new perspectives in evolutionary zoology. Our goal is to serve as a global publishing forum for fundamental researchers in all fields of zoology.