生物
转基因生物
基因分型
计算生物学
基因
基因组编辑
清脆的
转基因
基因型
遗传学
作者
Neeraj K. Aryal,Jan Parker-Thornburg
出处
期刊:Methods of Molecular Biology
日期:2020-01-01
卷期号:2066: 133-148
被引量:1
标识
DOI:10.1007/978-1-4939-9837-1_12
摘要
Prior to generating a new mouse model, it is important to plan the method that will be used to detect which of the mice generated have the mutation(s) desired. Nearly, all types of mutations may be detected using PCR. However, the choice of primers will differ depending upon the method used to generate the model. Transgenic mice should be genotyped across a unique junction fragment. Targeted ES cells used to generate knock-out or knock-in mice should be genotyped using primers from a unique marker in the construct and a region outside of the construct. Targeting in ES cells can also be detected using a genomic Southern blot. Mice targeted using CRISPR/Cas9 should have the region of interest amplified using PCR, and then be assessed for size changes (for large changes in sequence) by Surveyor Assay (for gene knock-out and point mutations) and/or sequenced to verify the mutation. Each of these models has a unique requirement for genotyping, and failure to understand the requirements can easily lead to loss of the gene in subsequent generations.
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