毒液
生物
蜘蛛
转录组
计算生物学
基因
毒素
蜘蛛毒素
进化生物学
遗传学
基因表达
动物
生物化学
受体
谷氨酸受体
作者
Tingcai Cheng,Renwen Long,Yuqian Wu,Youbing Guo,Duolian Liu,Li Peng,Daiqin Li,Daiwen Yang,Xin Xu,Fengxiang Liu,Qingyou Xia
标识
DOI:10.1111/1744-7917.12305
摘要
Tarantula venoms provide a model system for studying toxin selectivity, structure-activity relationships and molecular evolution of peptide toxins. Previous studies have identified a large number of peptide toxins in the venom of the Chinese bird spider Haplopelma hainanum, generally regarded as a highly venomous spider. However, the lack of available RNA-seq transcriptomic and genomic data is an obstacle to understanding its venom at the molecular level. In this study, we investigated the venom gland transcriptome of H. hainanum by RNA-seq, in the absence of an available genomic sequence. We identified 201 potential toxins among 57 181 de novo assembled transcripts, including knottins, Kunitz-type toxins, enzymes and other proteins. We systematically identified most of the knottins and Kunitz-type toxins, some of which showed strongly biased expression in the venom gland, including members of the huwentoxin-1, huwentoxin-2 and magi-1 families. We also discovered several novel potential toxins. These data demonstrate the high molecular and structural diversity in the venom toxins of H. hainanum. This study offers a useful strategy for exploring the complex components of spider venoms.
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