Ruocco Nadia, Costantini Susan, Zupo Valerio, Romano Giovanna, Ianora Adrianna, Fontana Angelo, Costantini Maria
Department of Biology and Evolution of Marine Organisms, Stazione Zoologica Anton Dohrn, Villa Comunale, Napoli, Italy.
Department of Biology, University of Naples Federico II, Complesso Universitario di Monte Sant'Angelo, Via Cinthia, Napoli, Italy.
PLoS One. 2017 Feb 15;12(2):e0172171. doi: 10.1371/journal.pone.0172171. eCollection 2017.
The sea urchin Paracentrotus lividus (Lamarck, 1816) is a keystone herbivore in the Mediterranean Sea due to its ability to transform macroalgal-dominated communities into barren areas characterized by increased cover of bare substrates and encrusting coralline algae, reduced biodiversity and altered ecosystem functions. P. lividus is also an excellent animal model for toxicology, physiology and biology investigations having been used for more than a century as a model for embryological studies with synchronously developing embryos which are easy to manipulate and analyze for morphological aberrations. Despite its importance for the scientific community, the complete genome is still not fully annotated. To date, only a few molecular tools are available and a few Next Generation Sequencing (NGS) studies have been performed. Here we aimed at setting-up an RNA extraction method to obtain high quality and sufficient quantity of RNA for NGS from P. lividus embryos at the pluteus stage. We compared five different RNA extraction protocols from four different pools of plutei (500, 1000, 2500 and 5000 embryos): TRIzol®, and four widely-used Silica Membrane kits, GenElute™ Mammalian Total RNA Miniprep Kit, RNAqueous® Micro Kit, RNeasy® Micro Kit and Aurum™ Total RNA Mini Kit. The quantity of RNA isolated was evaluated using NanoDrop. The quality, considering the purity, was measured as A260/A280 and A260/230 ratios. The integrity was measured by RNA Integrity Number (RIN). Our results demonstrated that the most efficient procedures were GenElute, RNeasy and Aurum, producing a sufficient quantity of RNA for NGS. The Bioanalyzer profiles and RIN values revealed that the most efficient methods guaranteeing for RNA integrity were RNeasy and Aurum combined with an initial preservation in RNAlater. This research represents the first attempt to standardize a method for high-quality RNA extraction from sea urchin embryos at the pluteus stage, providing a new resource for this established model marine organism.
紫球海胆(Paracentrotus lividus,拉马克,1816年)是地中海的一种关键食草动物,因为它能够将以大型藻类为主的群落转变为贫瘠区域,其特征是裸露基质和结壳珊瑚藻的覆盖增加、生物多样性降低以及生态系统功能改变。紫球海胆也是毒理学、生理学和生物学研究的优秀动物模型,在一个多世纪以来一直被用作胚胎学研究的模型,其胚胎同步发育,易于操作和分析形态畸变。尽管它对科学界很重要,但其完整基因组仍未得到充分注释。迄今为止,只有少数分子工具可用,且仅进行了一些下一代测序(NGS)研究。在这里,我们旨在建立一种RNA提取方法,以便从长腕幼虫阶段的紫球海胆胚胎中获得高质量和足够数量的RNA用于NGS。我们比较了来自四个不同长腕幼虫池(500、1000、2500和5000个胚胎)的五种不同RNA提取方案:TRIzol®,以及四种广泛使用的硅胶膜试剂盒,即GenElute™哺乳动物总RNA微量制备试剂盒、RNAqueous®微量试剂盒、RNeasy®微量试剂盒和Aurum™总RNA微量试剂盒。使用NanoDrop评估分离出的RNA的量。考虑到纯度,质量通过A260/A280和A260/230比值来衡量。完整性通过RNA完整性数(RIN)来衡量。我们的结果表明,最有效的方法是GenElute、RNeasy和Aurum,它们能产生足够数量的RNA用于NGS。生物分析仪图谱和RIN值表明,保证RNA完整性的最有效方法是RNeasy和Aurum,并结合在RNAlater中进行初始保存。这项研究是首次尝试标准化从长腕幼虫阶段的海胆胚胎中提取高质量RNA的方法,为这种成熟的海洋模式生物提供了新的资源。