Instituto de Ciências da Educação, Laboratório de Fisiologia e Toxinas animais, Universidade Federal do Oeste do Pará - UFOPA, Av. Marechal Rondon, S/N-Caranazal, CEP 68040-470 Santarém, Pará, Brazil.
Toxicon. 2012 Sep 15;60(4):539-50. doi: 10.1016/j.toxicon.2012.05.020. Epub 2012 Jun 5.
Sea anemone toxins are predominantly peptide and proteins that act mainly on sodium and potassium channels, as well as in a variety of target cells causing lysis. Over recent years, the number of sea anemone peptide toxins as well as cytolytic pore-forming proteins and phospholipase A(2) sequences submitted to databases has been rapidly increasing due to the developments in DNA sequencing technology and proteomic approaches. However, the lack of a systematic nomenclature has resulted in multiple names being assigned to the same toxins, toxins from unrelated species being designated by the same name, and ambiguous name designations. Therefore, in this work we propose a systematic nomenclature in which we adopted specific criteria, based on order of discovery and phylogenetic analysis, in order to avoid redundant sea anemone toxin names. Implementation of the nomenclature proposed here not only allowed us to rename the already published 191 anemone toxins without ambiguities, but it can be used to unambiguously name newly discovered toxins whether or not they are related to previously published sea anemone sequences. In the new nomenclature each toxin name contains information about the toxin's biological activity, origin and relationship to known isoforms. Ongoing increases in the speed of DNA sequencing will raise significantly the number of sea anemone toxin sequences in the literature. This will represent a constant challenge in their clear identification and logical classification, which could be solved using the proposed nomenclature.
海葵毒素主要是作用于钠钾通道的肽类和蛋白质,也会在各种靶细胞中引起溶解。近年来,由于 DNA 测序技术和蛋白质组学方法的发展,提交到数据库中的海葵肽毒素、胞溶孔形成蛋白和磷脂酶 A(2)序列的数量迅速增加。然而,由于缺乏系统的命名法,导致同一个毒素被赋予了多个名称,不同物种的毒素被指定了相同的名称,并且名称的指定也存在歧义。因此,在这项工作中,我们提出了一个系统命名法,我们根据发现的顺序和系统发生分析采用了特定的标准,以避免海葵毒素的名称重复。实施这里提出的命名法不仅允许我们重新命名已经发表的 191 种海葵毒素而不会产生歧义,而且可以用来明确命名新发现的毒素,无论它们是否与以前发表的海葵序列有关。在新的命名法中,每个毒素的名称都包含有关毒素的生物学活性、来源和与已知同工型关系的信息。随着 DNA 测序速度的不断提高,文献中海葵毒素序列的数量将会显著增加。这将对它们的明确识别和逻辑分类构成持续的挑战,而使用所提议的命名法可以解决这个问题。