Unusual stability of messenger RNA in snake venom reveals gene expression dynamics of venom replenishment

Currier, R, Calvete, JJ, Sanz, L, Harrison, RA, Rowley, PD and Wagstaff, SC (2012). Unusual stability of messenger RNA in snake venom reveals gene expression dynamics of venom replenishment. [Dataset]. PLOS One. https://doi.org/10.1371/journal.pone.0041888
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Data to support a publication on the dynamics of gene expression in synthesised venom proteins following venom depletion. Outputs include a gene expression analysis generated by quantitative PCR and minimum information on on Publication of Quantitative Real-time PCR Experiments (MIQE) guidelines.

Keywords

RNA, Snake venom, Venom replenishment

Figure_S1.tif
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Optimisation of venom quantitative PCR. Representative standard curves for snake venom metalloproteinase (SVMP) and C-type lectin (CTL) (1Ai and Aii) show high efficiency amplification of 94.0 and 96.6% respectively.
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Figure_S2.tif
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Raw data following gene expression analysis by quantitative PCR. Gene expression analysis conducted using the BioRad CFX manager software
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Table_S1.docx
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Minimum information for Publication of Quantitative Real-time PCR Experiments (MIQE) guidelines. Guidelines published by Bustin et al 2009 were referred to in order to ensure accuracy and reliability of quantitative PCR data
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Table_S2.docx
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Data
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Raw individual relative gene expression data generated by quantitative PCR. Raw qPCR data generated from relative expression analysis to show fold changes in expression of venom genes of interest, including snake venom metalloproteinase (SVMP)
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