建立基于自动化、高分辨率熔融分析以及为样本跟踪、数据分析和报告生成而专门开发的 MATLAB 应用程序的小鼠基因分型核心设施。

Comparative medicine Pub Date : 2024-08-01 Epub Date: 2024-05-25 DOI:10.30802/AALAS-CM-24-000014
Hagit Dafni, Kohava Levi, Miriam Chen Eldad, May Shaul, Roni Oren, Liat Alyagor, Noa Stettner, Alon Harmelin, Rebecca Haffner-Krausz
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引用次数: 0

摘要

内部基因分型设施应力求比外包服务更具成本效益,比个别研究小组的短期雇员或学生进行的基因分型更可靠。可靠的基因分型可以高效、经济地管理小鼠群体,促进研究结果的准确性和可重复性。在此,我们将详细介绍我们依靠自动 PCR 组装和高分辨率熔解(HRM)分析(第一衍生物)建立基因分型核心设施的方法。我们设计的工作流程由使用 MATLAB App Designer 开发的专门设计的应用程序严格管理,这些应用程序允许直接进行工作规划,确保在整个过程中跟踪样本,并为可靠的数据分析和生成基因分型报告提供平台。我们成功地将 250 多种不同目标基因的 PCR 产物分析从标准凝胶电泳过渡到了更先进的 HRM 分析。约有 23% 的目标基因需要重新设计引物以适应我们的方案。这一过程具有很强的通用性,只有 2% 的目标基因需要从标准 PCR 方法转向限制性更强的方案,以减少非特异性产物的扩增。目前,我们每周都会对断奶或实验终点时采集的样本进行 1000 多次 PCR 反应,并在每个 PCR 板中组装大量的目标基因。我们还发现,对囊胚细胞而非胚胎进行基因分型可作为冷冻保存的质量控制。因此,我们的基因分型方案提倡 3R(Replacement、Reduction 和 Refinement)原则。我们改进的基因分型过程有利于经济高效地管理菌落,用先进的方法取代组织类型和传统方法,并及时提供可靠的结果。MATLAB 代码和相关数据可在补充材料和网上获取。
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Establishing a Mouse Genotyping Core Facility Based on Automation, High-resolution Melting Analysis, and Purpose-developed MATLAB Applications for Sample Tracking, Data Analysis, and Report Generation.

An in-house genotyping facility should aim to be more cost-effective than outsourced service and more reliable than genotyping performed by short-term employees or students of individual research groups. Reliable genotyping allows efficient and economical management of mice colonies and promotes accurate and reproducible research results. Here we provide a detailed description of our approach to establishing a genotyping core facility, relying on automated PCR assembly and high-resolution melting (HRM) analysis (first derivative). The workflow we devised was tightly managed by purpose-designed applications developed using MATLAB App Designer that allowed straightforward work planning, ensured sample tracking throughout the process, and provided a platform for reliable data analysis and generation of genotyping reports. We successfully transitioned PCR product analysis of more than 250 different target genes from standard gel electrophoresis to the more advanced HRM analysis. About 23% of the target genes required a redesign of primers to adapt to our protocol. The process was highly universal, and only 2% of the target genes required deviation from the standard PCR method to a more restricted protocol that reduces the amplification of nonspecific products. We currently run more than 1,000 PCR reactions weekly, of samples taken at weaning or experimental endpoint, and assemble a large variety of target genes in every PCR plate. We also showed that genotyping of blastocytes instead of embryos can serve as quality control of cryopreservation. Thus, our genotyping protocol promotes the 3Rs (Replacement, Reduction, and Refinement) principles. Our refined genotyping process facilitates cost-effective colony management, replaces tissue types as well as traditional methods with advanced ones, and provides reliable results in a timely manner. MATLAB codes and related data are available in supplementary materials and online.

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