Growing oocytes accumulate maternal mRNA to support subsequent meiotic maturation and maternal-to-zygotic transition. However, the regulatory mechanisms governing the fate of these maternal mRNAs remain largely unknown. Here, we identified heterogeneous nuclear ribonucleoprotein M (hnRNPM) as a critical regulator of pre-mRNA alternative splicing during mouse oocyte development. Genetic ablation of hnRNPM leads to severe cytoplasmic defects, meiotic arrest, and complete female infertility. Using SCAN-seq, we uncovered novel transcript isoforms and systematically characterized hnRNPM-regulated alternative splicing events. Furthermore, LACE-seq revealed hnRNPM-binding sites at single-nucleotide resolution in oocytes, linking its RNA-binding activity to splicing fidelity. Additionally, hnRNPM interacts with BCAS2, a known splicing factor critical for oocyte development, and modulates its binding to pre-mRNA loci to precisely control the alternative splicing. Overall, our study not only uncover an essential role of hnRNPM in mammalian oocyte development and female fertility but also unveils a critical regulatory network governing alternative splicing during oocyte development.
hnRNPM cooperates with BCAS2 to modulate alternative splicing during oocyte development.
hnRNPM 与 BCAS2 协同作用,在卵母细胞发育过程中调节选择性剪接。
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| 期刊: | Nature Communications | 影响因子: | 15.700 |
| 时间: | 2026 | 起止号: | 2026 Feb 12; 17(1):2681 |
| doi: | 10.1038/s41467-026-69176-8 | 靶点: | NPM |
| 研究方向: | 发育与干细胞、细胞生物学 | ||
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