Qualitative and Quantitative Proteomic Analysis of Venoms from Mexican Rattlesnakes

  Qualitative and Quantitative Proteomic Analysis of Venoms from Mexican Rattlesnakes Abstract Despite the vast biodiversity of Mexican vipers, venom of endemic species has been barely studied. Here we analyzed the venom composition of three endemic species of rattlesnakes: Crotalus aquilus , C. triseriatus , and C. ravus . We used quantitative chromato-mass-spectrometry and compared venoms with C. molossus , a species commonly found in North America, in a comparative and phylogenetic framework. In total, we identified 165 proteins grouped in 19 main protein families, consistent with previous reports for viperid venoms. In C. aquilus and C. triseriatus , the most predominant protein-family type was Serine Proteases, and in C. triseriatus and C. molossus it was Snake Venom Metalloproteases. The Label-free quantification revealed a high proportion of Snake Venom Metalloproteases in C. aquilus , C. triseriatus , and C. molossus , reaching 28–47% of the total venom. In contrast, in ...

Efficiency of five RNA extraction protocols for Grammostola actaeon (Pocock, 1903) small spinneret tissue samples

 


Efficiency of five RNA extraction protocols for Grammostola actaeon (Pocock, 1903) small spinneret tissue samples

Abstract

Systemic optimization of RNA extraction protocols in non-model arachnids is indispensable for gene expression studies, including transcriptome sequencing and analyses. Spinnerets of the Neotropical tarantula Grammostola actaeon (Pocock, 1903) (family Theraphosidae) were used to evaluate the performance of two RNA extraction reagents and three commercially available kits for isolating total RNA from small eukaryotic tissue samples. Total RNA was extracted from spinneret tissues, using two samples for each method. We used the commercially available reagents TRIzol and NucleoZOL and the RNA extraction kits NucleoSpin and NucleoSpin XS (Macherey Nagel) and Total RNA Purification Kit (Norgen Biotek Corp). Quantification using Qubit revealed that NucleoSpin, Norgen, and NucleoSpin XS resulted in the highest RNA yields respectively, while Nanodrop analysis ranked Norgen, TRIzol, NucleoSpin, NucleoSpin XS in descending order. Bioanalyzer analysis indicated that Nucleospin, and NucleoSpin XS delivered the best results for our samples. While each method successfully yielded sufficient RNA for RNA-seq experiments, variations in RNA quality among methods indicate differences in their suitability for specific applications. Our data provide further evidence that RNA integrity number (RIN)-based assessments in G. actaeon may not be reliable for evaluating RNA quality due to a widespread occurrence of the ‘gap deletion’ phenomenon in arthropods. RNA from species with 28S rRNA collapsed can yield high-quality transcriptomes, suggesting that current RIN-based assessments may not be reliable for evaluating RNA quality in many non-model invertebrates. Overall, differences in results of commercially available RNA extraction reagents/kits should be considered when selecting the most appropriate RNA extraction method for gene expression analysis.

Nancy Lo-Man-Hung, Sónia Cristina da Silva Andrade, Prashant Sharma, Tatiana Teixeira Torres, Federico D. Brown "Efficiency of five RNA extraction protocols for Grammostola actaeon (Pocock, 1903) small spinneret tissue samples," The Journal of Arachnology, 53(2), 118-124, (25 September 2025) https://doi.org/10.1636/JoA-S-24-023