Razak Muhammad Raznisyafiq, Aris Ahmad Zaharin, Md Yusoff Fatimah, Yusof Zetty Norhana Balia, Kim Sang Don, Kim Kyoung Woong
Faculty of Forestry and Environment, Department of Environment, Universiti Putra Malaysia, Selangor, Malaysia.
International Institute of Aquaculture and Aquatic Sciences, Universiti Putra Malaysia, Negeri Sembilan, Malaysia.
PLoS One. 2022 Apr 26;17(4):e0264989. doi: 10.1371/journal.pone.0264989. eCollection 2022.
The usage of cladocerans as non-model organisms in ecotoxicological and risk assessment studies has intensified in recent years due to their ecological importance in aquatic ecosystems. The molecular assessment such as gene expression analysis has been introduced in ecotoxicological and risk assessment to link the expression of specific genes to a biological process in the cladocerans. The validity and accuracy of gene expression analysis depends on the quantity, quality and integrity of extracted ribonucleic acid (RNA) of the sample. However, the standard methods of RNA extraction from the cladocerans are still lacking. This study evaluates the extraction of RNA from tropical freshwater cladocerans Moina micrura using two methods: the phenol-chloroform extraction method (QIAzol) and a column-based kit (Qiagen Micro Kit). Glycogen was introduced in both approaches to enhance the recovery of extracted RNA and the extracted RNA was characterised using spectrophotometric analysis (NanoDrop), capillary electrophoresis (Bioanalyzer). Then, the extracted RNA was analysed with reverse transcription polymerase chain reaction (RT-PCR) to validate the RNA extraction method towards downstream gene expression analysis. The results indicate that the column-based kit is most suitable for the extraction of RNA from M. micrura, with the quantity (RNA concentration = 26.90 ± 6.89 ng/μl), quality (A260:230 = 1.95 ± 0.15, A280:230 = 1.85 ± 0.09) and integrity (RNA integrity number, RIN = 7.20 ± 0.16). The RT-PCR analysis shows that the method successfully amplified both alpha tubulin and actin gene at 33-35 cycles (i.e. Ct = 32.64 to 33.48). The results demonstrate that the addition of glycogen is only suitable for the phenol-chloroform extraction method. RNA extraction with high and comprehensive quality control assessment will increase the accuracy and reliability of downstream gene expression, thus providing more ecotoxicological data at the molecular biological level on other freshwater zooplankton species.
近年来,由于枝角类动物在水生生态系统中的生态重要性,其作为非模式生物在生态毒理学和风险评估研究中的应用日益增加。分子评估如基因表达分析已被引入生态毒理学和风险评估中,以将特定基因的表达与枝角类动物的生物过程联系起来。基因表达分析的有效性和准确性取决于样品中提取的核糖核酸(RNA)的数量、质量和完整性。然而,从枝角类动物中提取RNA的标准方法仍然缺乏。本研究使用两种方法评估从热带淡水枝角类动物微型裸腹溞中提取RNA:酚-氯仿提取法(QIAzol)和基于柱的试剂盒(Qiagen Micro Kit)。两种方法都引入了糖原以提高提取RNA的回收率,并使用分光光度分析(NanoDrop)、毛细管电泳(Bioanalyzer)对提取的RNA进行表征。然后,用逆转录聚合酶链反应(RT-PCR)分析提取的RNA,以验证RNA提取方法对下游基因表达分析的适用性。结果表明,基于柱的试剂盒最适合从微型裸腹溞中提取RNA,其数量(RNA浓度 = 26.90 ± 6.89 ng/μl)、质量(A260:230 = 1.95 ± 0.15,A280:230 = 1.85 ± 0.09)和完整性(RNA完整性数值,RIN = 7.20 ± 0.16)。RT-PCR分析表明,该方法在33 - 35个循环(即Ct = 32.64至33.48)成功扩增了α微管蛋白和肌动蛋白基因。结果表明,糖原的添加仅适用于酚-氯仿提取法。具有高质量和全面质量控制评估的RNA提取将提高下游基因表达的准确性和可靠性,从而在分子生物学水平上提供更多关于其他淡水浮游动物物种的生态毒理学数据。