Neuroscience Institute, University of Chicago, Chicago, IL 60637, USA.
Department of Psychology, University of Chicago, Chicago, IL 60637, USA.
Biotechniques. 2024;76(6):275-283. doi: 10.2144/btn-2024-0023. Epub 2024 Apr 23.
DNA collection is essential for genotyping laboratory animals. Common collection methods require tissue amputation, causing discomfort and injury. Rectal swabbing has been proposed as an effective, minimally invasive alternative, but an evidence-backed protocol for the technique remains unavailable. This report evaluates the effects of collection parameters on the quality of PCR results and presents a protocol for genotyping a litter of rats within 3-5 h. Samples with 2-8 scrapes produced enough DNA to amplify targets up to ∼1800 bp long using PCR. Rectal swabbing produced PCR results with similar utility as ear clip samples, and results were unaffected by residual fecal matter or cell debris. The protocol enables fast, minimally invasive and repeatable genotyping using commercial PCR reagents.
DNA 采集对于基因分型实验动物至关重要。常见的采集方法需要组织截肢,会引起不适和损伤。直肠拭子已被提出作为一种有效、微创的替代方法,但该技术仍缺乏有证据支持的方案。本报告评估了采集参数对 PCR 结果质量的影响,并提出了一种在 3-5 小时内对大鼠窝进行基因分型的方案。使用 PCR 进行扩增时,采集 2-8 次拭子即可获得足够的 DNA 来扩增长达约 1800bp 的靶标。直肠拭子产生的 PCR 结果与耳夹样本一样有效,并且结果不受残余粪便或细胞碎片的影响。该方案可使用商业 PCR 试剂实现快速、微创和可重复的基因分型。