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基于多重PCR靶向二代测序的近交系小鼠遗传质量监测方法建立 被引量:8

Mouse Genetic Quality Monitoring Method Establishment Based on Next-generation Sequencing through Multiplex PCR
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摘要 目的建立基于多重PCR靶向二代测序的小鼠遗传质量监测方案。方法从小鼠单核苷酸多态性(SNP)数据库筛选出相对均匀分布在20条染色体上的112个SNP位点,然后对SNP位点附近片段进行多重PCR扩增,建库后进行Illumina高通量测序,对原始测序数据进行生物信息学分析获得SNP信息。结果测序结果显示,多重PCR的扩增子均一性好,各片段成功率高达90%以上,特异性高,高深度测序条件下, SNP位点的等位基因比例趋近于1或0,符合纯合子条件;分析4批近交系小鼠样本,表明SNP位点成功鉴定的比例分别为99.82%, 92.00%, 99.10%和90.35%,且所有小鼠品系个体的SNP位点均为纯合,并被成功确定为目标品系;品系间两两比较,最大差异数为73个,最小差异数为3个,差异位点平均数为53个,差异中位数为60个,显示出本方案对常见近交系小鼠品系分辨率较高。结论多重PCR靶向二代测序方案的SNP分型方案是一种准确、快速、高效的基因分型方案,可用于遗传质量检测和品系鉴定。 Objective To establish a multiplex PCR targeting next-generation sequencing for mouse genetic quality monitoring. Methods Firstly, 112 single nucleotide polymorphisms(SNPs) on 20 chromosomes were screened from common inbred mice. Then, multiplex PCR amplification was performed on the fragments near the SNPs. After the library was constructed, high-throughput sequencing on Illumina platform was performed. The data was analyzed in a bioinformatics pipeline to obtain SNP information. Results The sequencing results showed that the uniform depth of amplicon was obtained,and the success calling rate of each site was over 90%. Secondly, under high specificity and high-depth sequencing conditions, the allele ratio of SNP sites approached 1 or zero, which is consistent with homozygous conditions. After 4 batches of mouse samples(98 in total) were analyzed, the proportions of SNP sites successfully identified were 99.82%, 92.00%, 99.10% and 90.35%, respectively. All mouse individuals were found to be homozygous and were successfully identified as the target strain. Compared differences between each pair strains, the maximum number of difference was 73, the minimum number was 3, and the average number was 53. The median number of difference was 60, showing our approach has a higher resolution for common inbred mouse strains. Conclusion The SNP typing scheme of the multiple PCR protocol is an accurate, rapid and efficient genotyping program for genetic quality testing and strains identification.
作者 钱强 徐园 王亚恒 周宇荀 肖君华 韩琳 鲍世民 李凯 QIAN Qiang;XU Yuan;WANG Ya-heng;ZHOU Yu-xun;XIAO Jun-hua;HAN Ling;BAO Shi-ming;LI Kai(Institute of Biological Science and Biotechnology,Donghua University,Shanghai 201620,China;Shanghai Tenth People's Hospital,Shanghai 200072,China;Shanghai Institutes for Biological Sciences,China Academy of Science,Shanghai 2000031,China)
出处 《实验动物与比较医学》 CAS 2019年第2期111-117,共7页 Laboratory Animal and Comparative Medicine
基金 上海市创新行动计划课题(编号:17140903100)
关键词 多重PCR 单核苷酸多态性(SNP) 近交系小鼠 靶向二代测序 遗传质量监测 Multiplex PCR Single nucleotide polymorphisms(SNPs) Inbred mice Targeted next-generation sequencing Genetic quality control
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