免疫球蛋白轻链
互补DNA
分子生物学
基因
生物
桑格测序
单元格排序
CD19
基因组
细胞
遗传学
计算生物学
抗体
DNA测序
作者
Xinyang Li,Peiyao Yang,Naibo Yang
出处
期刊:PubMed
日期:2018-04-01
卷期号:34 (4): 367-372
被引量:1
摘要
Objective To develop a set of methods of amplifying the natural paring heavy and light chain genes from one single B cell. Methods Yanhuang (YH) cells were the first whole genome sequenced human cells of Asian origin. With the immortalized cell lines as the raw material, single CD19+ B cells were sorted into individual PCR tubes by fluorescence-activated cell sorting (FACS). Then its total RNA was released by the lysis buffer, and reverse transcribed. With the cDNA as the templates, the pairing heavy and light chains from the same B cells were amplified by two-step nested PCRs to acquire their variable region sequences. Results Amplifying methodology has been successfully developed for acquiring single cell BCR genes, and the success rate was greater than 80%. The sorted single B cells could be saved in -80DegreesCelsius for up to two weeks, and then successfully amplified. The PCR products in the same tube were TA-cloned and identified by Sanger sequencing, including the heavy and light chain pairing information. A set of effective primers were reported and released in this study. Conclusion A set of methods were successfully developed for amplifying the natural paring heavy and light genes with the beginning of one single B cell.
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