RIP was performed using the EZ-Magna RIP Kit (Millipore). Cells (1 × 107) were lysed with RIP lysis buffer. Cell extracts were coimmunoprecipitated with anti-WDR5, EZH2, LSD1, SETDB1 (Cell Signaling Technology), or DNMT1 (Abcam), and the retrieved RNA was subjected to RT-qPCR analysis. For RT-qPCR analysis, U1 was used as a nonspecific control target.

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