ExtFig6A_RACE_BCAP31_R2_LG341.sgd

HEK293T ishXrn1 cells were treated with doxycycline for 3-4 days to induce knock down of Xrn1, then transfected with the luciferase reporters containing 99 bp, 51 bp, 27 bp or 15 bp insertions from the BCAP31 or SLC7A5 genes, and where indicated, with PR8 PA-X. RNA was extracted and used to run 5’ RACE with primers annealing to luciferase sequences. DNA bands were purified and sequenced to confirm their identities

将HEK293T ishXrn1细胞用多西环素处理3~4天以诱导Xrn1基因敲低，随后转染携带BCAP31或SLC7A5基因来源的99 bp、51 bp、27 bp或15 bp插入片段的荧光素酶报告基因载体；当实验中进行了标注时，同时共转染PR8 PA-X。提取细胞总RNA后，使用与荧光素酶序列互补的引物开展5'末端快速扩增（5' RACE），随后纯化DNA条带并测序以确认其序列同一性。