m6A modification of a 3' UTR site reduces RME1 mRNA levels to promote meiosis

We performed m6A-seq on 5h meiotic yeast from WT and ime4-cat background (IP and input), and RNA-seq on total and polysome RNA of 5h meiotic yeast from WT, ime4-cat, and rme1-10 backgrounds Overall design: 12 yeast m6A-seq samples, 18 yeast RNA-seq samples

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Bushkin GG, Pincus D, Morgan JT, Richardson K, Lewis C, Chan SH, Bartel DP, Fink GR