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m6A demethylase OsALKBH5 is required for double-strand break formation and repair by affecting mRNA stability in rice meiosis
New Phytologist ( IF 8.3 ) Pub Date : 2024-07-24 , DOI: 10.1111/nph.19976
Feiyang Xue 1 , Jie Zhang 1 , Di Wu 2 , Shiyu Sun 1 , Ming Fu 1 , Jie Wang 1 , Iain Searle 3 , Hongbo Gao 2 , Wanqi Liang 1, 4
Affiliation  

  • N6-methyladenosine (m6A) RNA modification is the most prevalent messenger RNA (mRNA) modification in eukaryotes and plays critical roles in the regulation of gene expression. m6A is a reversible RNA modification that is deposited by methyltransferases (writers) and removed by demethylases (erasers). The function of m6A erasers in plants is highly diversified and their roles in cereal crops, especially in reproductive development essential for crop yield, are largely unknown.
  • Here, we demonstrate that rice OsALKBH5 acts as an m6A demethylase required for the normal progression of male meiosis.
  • OsALKBH5 is a nucleo-cytoplasmic protein, highly enriched in rice anthers during meiosis, that associates with P-bodies and exon junction complexes, suggesting that it is involved in regulating mRNA processing and abundance. Mutations of OsALKBH5 cause reduced double-strand break (DSB) formation, severe defects in DSB repair, and delayed meiotic progression, leading to complete male sterility. Transcriptome analysis and m6A profiling indicate that OsALKBH5-mediated m6A demethylation stabilizes the mRNA level of multiple meiotic genes directly or indirectly, including several genes that regulate DSB formation and repair.
  • Our study reveals the indispensable role of m6A metabolism in post-transcriptional regulation of meiotic progression in rice.



中文翻译:


m6A 去甲基酶 OsALKBH5 通过影响水稻减数分裂中 mRNA 的稳定性来形成和修复双链断裂



  • N 6 -甲基腺苷 (m 6 A) RNA 修饰是真核生物中最常见的信使 RNA (mRNA) 修饰,在基因表达调控中发挥着关键作用。 m 6 A 是一种可逆的 RNA 修饰,由甲基转移酶(写入酶)沉积并由去甲基酶(擦除酶)去除。 m 6 A擦除器在植物中的功能高度多样化,并且它们在谷类作物中的作用,特别是在对作物产量至关重要的生殖发育中的作用,很大程度上是未知的。

  • 在这里,我们证明水稻 OsALKBH5 充当雄性减数分裂正常进展所需的 m 6 A 去甲基酶。

  • OsALKBH5 是一种核胞质蛋白,在减数分裂过程中在水稻花药中高度富集,与 P 体和外显子连接复合物相关,表明它参与调节 mRNA 加工和丰度。 OsALKBH5突变会导致双链断裂 (DSB) 形成减少、DSB 修复严重缺陷以及减数分裂进程延迟,从而导致完全雄性不育。转录组分析和 m 6 A 分析表明 OsALKBH5 介导的 m 6 A 去甲基化直接或间接稳定了多个减数分裂基因的 mRNA 水平,包括调节 DSB 形成和修复的几个基因。

  • 我们的研究揭示了 m 6 A 代谢在水稻减数分裂进程的转录后调控中不可或缺的作用。

更新日期:2024-07-24
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