首页> 外文期刊>Journal of Molecular Evolution >Structural and Molecular Diversification of the Anguimorpha Lizard Mandibular Venom Gland System in the Arboreal Species Abronia graminea
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Structural and Molecular Diversification of the Anguimorpha Lizard Mandibular Venom Gland System in the Arboreal Species Abronia graminea

机译:树木物种Abronia graminea的Anguimorpha蜥蜴下颌下腺腺体系统的结构和分子多样性。

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In the past, toxinological research on reptiles has focused principally on clinically important species. As a result, our understanding of the evolution of the reptile venom system is limited. Here, for the first time, we describe the structural and molecular evolutionary features of the mandibular toxin-secreting gland of Abronia graminea, a representative of one of the poorly known and entirely arboreal lineages of anguimorph lizards. We show that the mandibular gland is robust and serous, characters consistent with those expected of a toxin-secreting gland in active use. A wide array of transcripts were recovered that were homologous to those encoded by the indisputably venomous helodermatid lizards. We show that some of these toxin transcripts are evolving under active selection and show evidence of rapid diversification. Helokinestatin peptides in particular are revealed to have accumulated residues that have undergone episodic diversifying selections. Conversely, the natriuretic peptides have evolved under tremendous evolutionary constraints despite being encoded in tandem with helokinestatins by the same gene precursor. Of particular note is the sequencing for the first time of kunitz peptides from a lizard toxin-secreting gland. Not only are kunitz peptides shown to be an ancestral toxicoferan toxin, the ancestral state of this peptide is revealed to be a dual domain encoding precursor. This research provides insight into the evolutionary history of the ancient toxicoferan reptile venom system. In addition, it shows that even ‘clinically irrelevant’ species can be a rich source of novel venom components, worthy of investigation for drug design and biomedical research.
机译:过去,爬行动物的毒理学研究主要集中于临床上重要的物种。结果,我们对爬行动物毒液系统进化的理解是有限的。在这里,我们第一次描述了Abronia graminea的下颌分泌毒素腺体的结构和分子进化特征,它是anguimorph蜥蜴的一个鲜为人知且完全是树栖的世系之一的代表。我们显示,下颌腺健壮且呈浆液状,其特征与预期使用的分泌毒素腺体一致。回收了大量的转录本,这些转录本与无毒的嗜血性蜥蜴编码的那些同源。我们表明,这些毒素转录物中的一些正在主动选择下进化,并显示出迅速多样化的证据。尤其是Helokinestatin肽显示具有累积的残基,这些残基经历了情节多样化的选择。相反,尽管相同基因前体与促尿激素抑制素串联编码,但利钠肽却在巨大的进化限制下进化。特别值得注意的是首次从分泌蜥蜴毒素的腺体中对kunitz肽进行测序。不仅kunitz肽被证明是一种祖先的铁氧体毒素,而且该肽的祖先状态也被证明是编码双域的前体。这项研究提供了远古的毒铁蛋白爬行动物毒液系统的进化历史的见解。此外,它表明,即使“与临床无关”的物种也可以成为新颖毒液成分的丰富来源,值得进行药物设计和生物医学研究。

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