Jacquot Sylvie, Chartoire Nathalie, Piguet Françoise, Hérault Yann, Pavlovic Guillaume
Institut Clinique de la Souris, PHENOMIN-ICS, Illkirch, France.
NeuroGenCell Thérapie Génique et Cellulaire des Maladies Neurodégénératives de l'Adulte et de l'Enfant, INSERM U1127, Institut du Cerveau et de la Moelle Épinière (ICM), Paris, France.
Curr Protoc Mouse Biol. 2019 Dec;9(4):e65. doi: 10.1002/cpmo.65.
Genotyping consists of searching for a DNA sequence variation localized at a well-defined locus in the genome. It is an essential step in animal research because it allows the identification of animals that will be bred to generate and maintain a colony, euthanized to control the available space in the animal facility, or used in experiment protocols. Here we describe polymerase chain reaction (PCR) genotyping protocols for fast, sensitive, easy, and cost-effective characterization of mouse genotype. We discuss optimization of parameters to improve the reliability of each assay and propose recommendations for enhancing reproducibility and reducing the occurrence of inconclusive genotyping. All steps required for efficient genotyping are presented: tissue collection; sample verification and direct DNA lysis; establishment of a robust genotyping strategy with reliable, rapid, and cost-effective assays; and finally, transition to high-throughput automatized PCR, including mix miniaturization and automation. © 2019 The Authors. Basic Protocol 1: Tissue sampling methods and procedure Basic Protocol 2: Sample verification and DNA lysis Basic Protocol 3: Design of a genotyping strategy Basic Protocol 4: Moving to high-throughput genotyping.
基因分型包括寻找位于基因组中明确界定位点的DNA序列变异。它是动物研究中的一个重要步骤,因为它能够识别用于繁殖以建立和维持种群、实施安乐死以控制动物设施可用空间或用于实验方案的动物。在此,我们描述了用于快速、灵敏、简便且经济高效地鉴定小鼠基因型的聚合酶链反应(PCR)基因分型方案。我们讨论了参数优化以提高每个检测的可靠性,并提出了提高重现性和减少不确定基因分型发生的建议。介绍了高效基因分型所需的所有步骤:组织采集;样本验证和直接DNA裂解;采用可靠、快速且经济高效的检测方法建立稳健的基因分型策略;最后,过渡到高通量自动化PCR,包括混合体系微型化和自动化。© 2019作者。基本方案1:组织采样方法和程序 基本方案2:样本验证和DNA裂解 基本方案3:基因分型策略的设计 基本方案4:转向高通量基因分型