Key Laboratory of Combinatorial Biosynthesis and Drug Discovery, Ministry of Education, School of Pharmaceutical Sciences, Wuhan University, Wuhan, China.
School of Resources and Environmental Engineering, Wuhan University of Technology, Wuhan, China.
Gene. 2020 Dec 30;763:145048. doi: 10.1016/j.gene.2020.145048. Epub 2020 Aug 14.
Cross-contamination of cell lines is a highly relevant and pervasive problem. The analysis of short tandem repeats (STR) is a simple and commercially available technique to authenticate cell lines for more than two decades. At present, STR multiple amplification kits have been developed up to 21 loci while the current STR databases only provide 9-loci STR profiles. Here, we compared the advantages of 21-loci STR methodology using the same algorithm as 9-loci method. The 21-loci method reduced the uncertainty ratio for authentications by 97.5% relative to the 9-loci method and exclude effectively false positive. We show that the additional 12 loci helped to greatly reduce sample-site marker specificity arising from genetic isolation and the occurrence of null alleles, suggesting that inclusion of additional loci in these databases will ultimately improve the efficiency and accuracy of authentication of cell lines. Taken together, we demonstrate the utility of a 21-loci method in human cells, providing a novel marker panel for use as a valuable alternative to 9-loci analyses to minimize cell line authentication errors and reduce costs due to erroneous experiments.
细胞系交叉污染是一个高度相关且普遍存在的问题。短串联重复序列(STR)分析是一种简单且可商用的技术,可在二十多年来对细胞系进行身份验证。目前,STR 多重扩增试剂盒已开发至 21 个位点,而当前的 STR 数据库仅提供 9 个位点 STR 图谱。在这里,我们比较了使用与 9 个位点方法相同算法的 21 个位点 STR 方法的优势。与 9 个位点方法相比,21 个位点方法将鉴定的不确定性比率降低了 97.5%,并有效地排除了假阳性。我们表明,额外的 12 个位点有助于大大降低由于遗传隔离和无效等位基因的出现而导致的样本位点标记特异性,这表明在这些数据库中包含额外的位点最终将提高细胞系鉴定的效率和准确性。总之,我们证明了 21 个位点方法在人类细胞中的实用性,提供了一个新的标记面板,可作为 9 个位点分析的有价值替代方法,以最大程度地减少细胞系鉴定错误并降低因错误实验而导致的成本。