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Functional and structural diversification of the Anguimorpha lizard venom system.

机译:Anguimorpha蜥蜴毒液系统的功能和结构多样化。

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Venom has only been recently discovered to be a basal trait of the Anguimorpha lizards. Consequently, very little is known about the timings of toxin recruitment events, venom protein molecular evolution, or even the relative physical diversifications of the venom system itself. A multidisciplinary approach was used to examine the evolution across the full taxonomical range of this approximately 130 million-year-old clade. Analysis of cDNA libraries revealed complex venom transcriptomes. Most notably, three new cardioactive peptide toxin types were discovered (celestoxin, cholecystokinin, and YY peptides). The latter two represent additional examples of convergent use of genes in toxic arsenals, both having previously been documented as components of frog skin defensive chemical secretions. Two other novel venom gland-overexpressed modified versions of other protein frameworks were also recovered from the libraries (epididymal secretory protein and ribonuclease). Lectin, hyaluronidase, and veficolin toxin types were sequenced for the first time from lizard venoms and shown to be homologous to the snake venom forms. In contrast, phylogenetic analyses demonstrated that the lizard natriuretic peptide toxins were recruited independently of the form in snake venoms. The de novo evolution of helokinestatin peptide toxin encoding domains within the lizard venom natriuretic gene was revealed to be exclusive to the helodermatid/anguid subclade. New isoforms were sequenced for cysteine-rich secretory protein, kallikrein, and phospholipase A(2) toxins. Venom gland morphological analysis revealed extensive evolutionary tinkering. Anguid glands are characterized by thin capsules and mixed glands, serous at the bottom of the lobule and mucous toward the apex. Twice, independently this arrangement was segregated into specialized serous protein-secreting glands with thick capsules with the mucous lobules now distinct (Heloderma and the Lanthanotus/Varanus clade). The results obtained highlight the importance of utilizing evolution-based search strategies for biodiscovery and emphasize the largely untapped drug design and development potential of lizard venoms.
机译:毒液直到最近才被发现是Anguimorpha蜥蜴的基本特征。因此,对毒素募集事件,毒液蛋白分子进化甚至毒液系统本身的相对物理多样性的时间了解甚少。一种多学科的方法被用来研究这个大约1.3亿年历史的进化枝在整个分类学范围内的演变。 cDNA文库的分析揭示了复杂的毒液转录组。最值得注意的是,发现了三种新的心脏活性肽毒素类型(塞来毒素,胆囊收缩素和YY肽)。后两个代表在有毒武器库中基因的融合使用的其他例子,这两个文献先前都已被证明是青蛙皮肤防御性化学分泌物的组成部分。还从文库中回收了其他两个新的构架的新的毒腺过表达的修饰版本(附睾分泌蛋白和核糖核酸酶)。首次从蜥蜴毒液中对凝集素,透明质酸酶和veficolin毒素类型进行了测序,结果显示它们与蛇毒液形式同源。相反,系统发育分析表明,蜥蜴利钠肽毒素的募集独立于蛇毒的形式。揭示了蜥蜴毒利钠基因中的编码角蛋白激酶肽毒素结构域的从头进化是独有的对皮炎/血管性皮下皮。新的同工型测序富含半胱氨酸的分泌蛋白,激肽释放酶和磷脂酶A(2)毒素。毒腺形态学分析揭示了广泛的进化修补。 Anguid腺的特征是薄囊和混合腺,在小叶的底部呈浆液状,粘膜朝向先端。两次独立地,将这种排列分离成具有厚囊的专门分泌浆液性蛋白的腺体,粘膜小叶现已明显(Heloderma and Lanthanotus / Varanus clade)。获得的结果突出了利用基于进化的搜索策略进行生物发现的重要性,并强调了蜥蜴毒液尚未开发的药物设计和开发潜力。

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