ALKBH5 controls the meiosis-coupled mRNA clearance in oocytes by removing the N 6 -methyladenosine methylation.
Long BaiYu XiangMinyue TangShuangying LiuQingqing ChenQichao ChenMin ZhangShan WanYimiao SangQingfang LiSisi WangZhekun LiYang SongXiaoling HuLuna MaoGuofang FengLong CuiYinghui YeYi-Min ZhuPublished in: Nature communications (2023)
N 6 -methyladenosine (m 6 A) maintains maternal RNA stability in oocytes. One regulator of m 6 A, ALKBH5, reverses m 6 A deposition and is essential in RNA metabolism. However, the specific role of ALKBH5 in oocyte maturation remains elusive. Here, we show that Alkbh5 depletion causes a wide range of defects in oocyte meiosis and results in female infertility. Temporal profiling of the maternal transcriptomes revealed striking RNA accumulation in Alkbh5 -/- oocytes during meiotic maturation. Analysis of m 6 A dynamics demonstrated that ALKBH5-mediated m 6 A demethylation ensures the timely degradation of maternal RNAs, which is severely disrupted following Alkbh5 -/- depletion. A distinct subset of transcripts with persistent m 6 A peaks are recognized by the m 6 A reader IGF2BP2 and thus remain stabilized, resulting in impaired RNA clearance. Additionally, reducing IGF2BP2 in Alkbh5-depleted oocytes partially rescued these defects. Overall, this work identifies ALKBH5 as a key determinant of oocyte quality and unveil the facilitating role of ALKBH5-mediated m 6 A removal in maternal RNA decay.