SRX13569533 GSM5766808_r1 SRP353044 PRJNA793437 SRS11461993 GSM5766808 GSM5766808 RIP-Seq TRANSCRIPTOMIC other After cross-link with UV, the cells were collected by trypsinization, lysed in 1 ml M-PER buffer (78501, Thermo Fisher Scientific) with 100 U/ml RNase inhibitor and 1 × protease inhibitor on ice for 20 min, and sonicated in a Bioruptor Pico device (Diagenode) with 30s on/30s off for 10 cycles. Then the lysates were collected and subject to RIP with Flag antibody and Protein A/G Magnetic Beads. The RIP RNAs were recovered from the beads with RNA clean and concentrater kit. Both Input and RIP RNAs were used for sequencing. KAPA Stranded mRNA-Seq Kit (Illumina Platforms) was utilized to construct library and sequencing was performed on an Illumina Hiseq 2500. Illumina HiSeq 2500 SRX13569534 GSM5766809_r1 SRP353044 PRJNA793437 SRS11461994 GSM5766809 GSM5766809 RIP-Seq TRANSCRIPTOMIC other After cross-link with UV, the cells were collected by trypsinization, lysed in 1 ml M-PER buffer (78501, Thermo Fisher Scientific) with 100 U/ml RNase inhibitor and 1 × protease inhibitor on ice for 20 min, and sonicated in a Bioruptor Pico device (Diagenode) with 30s on/30s off for 10 cycles. Then the lysates were collected and subject to RIP with Flag antibody and Protein A/G Magnetic Beads. The RIP RNAs were recovered from the beads with RNA clean and concentrater kit. Both Input and RIP RNAs were used for sequencing. KAPA Stranded mRNA-Seq Kit (Illumina Platforms) was utilized to construct library and sequencing was performed on an Illumina Hiseq 2500. Illumina HiSeq 2500 SRX13569535 GSM5766810_r1 SRP353044 PRJNA793437 SRS11461995 GSM5766810 GSM5766810 RIP-Seq TRANSCRIPTOMIC other After cross-link with UV, the cells were collected by trypsinization, lysed in 1 ml M-PER buffer (78501, Thermo Fisher Scientific) with 100 U/ml RNase inhibitor and 1 × protease inhibitor on ice for 20 min, and sonicated in a Bioruptor Pico device (Diagenode) with 30s on/30s off for 10 cycles. Then the lysates were collected and subject to RIP with Flag antibody and Protein A/G Magnetic Beads. The RIP RNAs were recovered from the beads with RNA clean and concentrater kit. Both Input and RIP RNAs were used for sequencing. KAPA Stranded mRNA-Seq Kit (Illumina Platforms) was utilized to construct library and sequencing was performed on an Illumina Hiseq 2500. Illumina HiSeq 2500 SRX13569536 GSM5766811_r1 SRP353044 PRJNA793437 SRS11461996 GSM5766811 GSM5766811 RIP-Seq TRANSCRIPTOMIC other After cross-link with UV, the cells were collected by trypsinization, lysed in 1 ml M-PER buffer (78501, Thermo Fisher Scientific) with 100 U/ml RNase inhibitor and 1 × protease inhibitor on ice for 20 min, and sonicated in a Bioruptor Pico device (Diagenode) with 30s on/30s off for 10 cycles. Then the lysates were collected and subject to RIP with Flag antibody and Protein A/G Magnetic Beads. The RIP RNAs were recovered from the beads with RNA clean and concentrater kit. Both Input and RIP RNAs were used for sequencing. KAPA Stranded mRNA-Seq Kit (Illumina Platforms) was utilized to construct library and sequencing was performed on an Illumina Hiseq 2500. Illumina HiSeq 2500