Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2148-8-196
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dc.titleAccelerated exchange of exon segments in Viperid three-finger toxin genes (Sistrurus catenatus edwardsii; Desert Massasauga)
dc.contributor.authorDoley, R.
dc.contributor.authorPahari, S.
dc.contributor.authorMackessy, S.P.
dc.contributor.authorKini, R.M.
dc.date.accessioned2014-10-27T08:20:50Z
dc.date.available2014-10-27T08:20:50Z
dc.date.issued2008
dc.identifier.citationDoley, R., Pahari, S., Mackessy, S.P., Kini, R.M. (2008). Accelerated exchange of exon segments in Viperid three-finger toxin genes (Sistrurus catenatus edwardsii; Desert Massasauga). BMC Evolutionary Biology 8 (1) : -. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2148-8-196
dc.identifier.issn14712148
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/99995
dc.description.abstractBackground. Snake venoms consist primarily of proteins and peptides showing a myriad of potent biological activities which have been shaped by both adaptive and neutral selective forces. Venom proteins are encoded by multigene families that have evolved through a process of gene duplication followed by accelerated evolution in the protein coding region. Results. Here we report five gene structures of three-finger toxins from a viperid snake, Sistrurus catenatus edwardsii. These toxin genes are structured similarly to elapid and hydrophiid three-finger toxin genes, with two introns and three exons. Both introns and exons show distinct patterns of segmentation, and the insertion/deletion of segments may define their evolutionary history. The segments in introns, when present, are highly similar to their corresponding segments in other members of the gene family. In contrast, some segments in the exons show high similarity, while others are often distinctly different among corresponding regions of the isoforms. Conclusion. Ordered, conserved exon structure strongly suggests that segments in corresponding regions in exons have been exchanged with distinctly different ones during the evolution of these genes. Such a "switching" of segments in exons may result in drastically altering the molecular surface topology and charge, and hence the molecular targets of these three-finger toxins. Thus the phenomenon of accelerated segment switch in exons to alter targeting (ASSET) may play an important role in the evolution of three-finger toxins, resulting in a family of toxins with a highly conserved structural fold but widely varying biological activities. © 2008 Doley et al; licensee BioMed Central Ltd.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1186/1471-2148-8-196
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.1186/1471-2148-8-196
dc.description.sourcetitleBMC Evolutionary Biology
dc.description.volume8
dc.description.issue1
dc.description.page-
dc.identifier.isiut000257684600001
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