首页> 外文期刊>Toxins >True Lies: Using Proteomics to Assess the Accuracy of Transcriptome-Based Venomics in Centipedes Uncovers False Positives and Reveals Startling Intraspecific Variation in Scolopendra subspinipes
【24h】

True Lies: Using Proteomics to Assess the Accuracy of Transcriptome-Based Venomics in Centipedes Uncovers False Positives and Reveals Startling Intraspecific Variation in Scolopendra subspinipes

机译:真实的谎言:使用蛋白质组学评估C中基于转录组的基因组学的准确性,发现假阳性并揭示Scolopendra亚菠菜的惊人种内变异。

获取原文
           

摘要

Centipede venoms have emerged as a rich source of novel bioactive compounds. However, most centipede species are commonly considered too small for venom extraction and transcriptomics is likely to be an attractive way of probing the molecular diversity of these venoms. Examining the venom composition of Scolopendra subspinipes , we test the accuracy of this approach. We compared the proteomically determined venom profile with four common toxin transcriptomic toxin annotation approaches: BLAST search against toxins in UniProt, lineage-specific toxins, or species-specific toxins and comparative expression analyses of venom and non-venom producing tissues. This demonstrated that even toxin annotation based on lineage-specific homology searches is prone to substantial errors compared to a proteomic approach. However, combined comparative transcriptomics and phylogenetic analysis of putative toxin families substantially improves annotation accuracy. Furthermore, comparison of the venom composition of S. subspinipes with the closely related S. subspinipes mutilans revealed a surprising lack of overlap. This first insight into the intraspecific venom variability of centipedes contrasts the sequence conservation expected from previous findings that centipede toxins evolve under strong negative selection. Our results highlight the importance of proteomic data in studies of even comparably well-characterized venoms and warrants caution when sourcing venom from centipedes of unknown origin.
机译:毒液已成为新型生物活性化合物的丰富来源。然而,大多数cent物种通常被认为对于毒液提取而言太小,转录组学可能是探索这些毒液分子多样性的一种有吸引力的方法。检查蛇蝎子亚种的毒液成分,我们测试了这种方法的准确性。我们将蛋白质组学确定的毒液概况与四种常见的毒素转录组毒素注释方法进行了比较:针对UniProt中的毒素,谱系特异性毒素或物种特异性毒素进行BLAST搜索,并对毒液和非毒液产生组织进行比较表达分析。这表明,即使是基于谱系特异性同源性搜索的毒素注释,与蛋白质组学方法相比也容易出现重大错误。然而,组合的比较转录组学和推定的毒素家族的系统发育分析大大提高了注释的准确性。此外,通过比较刺亚链球菌和紧密相关的短链沙门氏菌的毒液成分,发现了令人惊讶的无重叠现象。对into的种内毒液变异性的第一个见识与先前的发现预期的序列保守性形成对比,该发现是cent毒素在强烈的负选择下进化的。我们的结果凸显了蛋白质组学数据在甚至比较特征明确的毒液研究中的重要性,并且在从来源不明的中提取毒液时需要谨慎。

著录项

相似文献

  • 外文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号