| Literature DB >> 26678257 |
Ting-Cai Cheng1, Ren-Wen Long1, Yu-Qian Wu1, You-Bing Guo1, Duo-Lian Liu1, Li Peng1, Dai-Qin Li2, Dai-Wen Yang2, Xin Xu3,4, Feng-Xiang Liu4, Qing-You Xia1.
Abstract
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.Entities:
Keywords: Haplopelma hainanum; diversity; tarantula venom; toxin; transcriptome
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Year: 2016 PMID: 26678257 DOI: 10.1111/1744-7917.12305
Source DB: PubMed Journal: Insect Sci ISSN: 1672-9609 Impact factor: 3.262