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Deep venomics of the Pseudonaja genus reveals inter- and intra-specific variation

机译:假单胞菌属的深部病毒学揭示了种间和种内变异

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摘要

Australian elapid venom remains an under-investigated resource of novel bioactive peptides. In this study, the venom gland transcriptomes and proteomes of the Australian western brown snakes, Pseudonaja aspidorhyncha and Pseudonaja nuchalis, were compared to Pseudonaja textilis. A deep venomics strategy incorporating high throughput 454 pyrosequencing gave a total of 200,911 raw reads for the three venoms. Subsequent annotation identified 5716 transcripts from 20 different toxin families with inter-specific variation between species observed in eight of the less abundant families. Integration of each venom proteome with the corresponding annotated reads identified 65 isoforms from six toxin families; high sequence coverage highlighted subtle differences between sequences and intra and inter-specific variation between species. High quality MS/MS data identified unusual glycoforms with natriuretic peptides from P. aspidorhyncha and P. nuchaliscontaining O-linked trisaccharides with high homology to the glycosylated region of TNPc. Molecular evolutionary assessments indicated the accelerated evolution of all toxin families with the exception of both natriuretic peptides and P. aspidorhyncha PLA2s that were found to be evolutionarily constrained under purifying selection.pressures. This study has revealed a wide range of novel peptide sequences from six bioactive peptide families and highlights the subtle differences between toxins in these closely related species.
机译:澳大利亚的蛇毒毒液仍然是对新型生物活性肽的研究不足的资源。在这项研究中,将澳大利亚西部褐蛇的毒腺转录组和蛋白质组与假单胞菌进行了比较。Pseudonaja aspidorhyncha和Pseudonaja nuchalis。结合高通量454焦磷酸测序的深度病毒学策略可为三个毒液提供总计200,911的原始读数。随后的注释识别了来自20个不同毒素家族的5716个转录本,在八个较不丰富的家族中观察到的物种之间具有种间差异。将每个毒液蛋白质组与相应的注释读段整合,鉴定出来自六个毒素家族的65个亚型。高序列覆盖率突出了序列之间的细微差异以及物种之间的种内和种间变异。高质量的MS / MS数据确定了来自P. aspidorhyncha和P. nuchalis的利尿钠肽与TNPc糖基化区域具有高度同源性的异常糖型。分子进化评估表明,除了利尿肽和P. aspidorhyncha PLA2s外,所有毒素家族的进化都加速,这两种纯化被发现在纯化选择压力下受到进化限制。这项研究揭示了来自六个生物活性肽家族的多种新型肽序列,并突出了这些密切相关物种中毒素之间的细微差异。

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