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Nab2 RNA 结合蛋白抑制雌性神经元组织中转录本的 mA 甲基化和雄性特异性剪接。

The Nab2 RNA binding protein inhibits mA methylation and male-specific splicing of transcript in female neuronal tissue.

机构信息

Department of Biology, Emory University, Atlanta, United States.

Department of Cell Biology Emory University School of Medicine, Atlanta, United States.

出版信息

Elife. 2023 Jul 17;12:e64904. doi: 10.7554/eLife.64904.

Abstract

The polyadenosine RNA binding protein Nab2, which is orthologous to a human protein lost in a form of inherited intellectual disability, controls adult locomotion, axon projection, dendritic arborization, and memory through a largely undefined set of target RNAs. Here, we show a specific role for Nab2 in regulating splicing of ~150 exons/introns in the head transcriptome and focus on retention of a male-specific exon in the sex determination factor () that is enriched in female neurons. Previous studies have revealed that this splicing event is regulated in females by N6-methyladenosine (mA) modification by the Mettl3 complex. At a molecular level, Nab2 associates with pre-mRNA in neurons and limits mA methylation at specific sites. In parallel, reducing expression of the Mettl3, Mettl3 complex components, or the mA reader Ythdc1 rescues mutant phenotypes in flies. Overall, these data identify Nab2 as an inhibitor of mA methylation and imply significant overlap between Nab2 and Mettl3 regulated RNAs in neuronal tissue.

摘要

多聚腺苷酸 RNA 结合蛋白 Nab2 与一种在遗传性智力障碍形式中丢失的人类蛋白同源,通过一组尚未完全定义的靶 RNA 控制成年运动、轴突投射、树突分支和记忆。在这里,我们展示了 Nab2 在调节头转录组中约 150 个外显子/内含子剪接中的特定作用,并特别关注性别决定因子 () 中一个雄性特异性外显子的保留,该外显子在雌性神经元中富集。先前的研究表明,这种剪接事件在雌性中由 Mettl3 复合物的 N6-甲基腺苷 (mA) 修饰调节。在分子水平上,Nab2 与神经元中的 pre-mRNA 结合,并限制特定位点的 mA 甲基化。同时,降低 Mettl3、Mettl3 复合物成分或 mA 读码器 Ythdc1 的表达可挽救 突变体在 果蝇中的表型。总的来说,这些数据表明 Nab2 是 mA 甲基化的抑制剂,并暗示 Nab2 和 Mettl3 调节的 RNA 在神经元组织中有显著的重叠。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d80b/10351920/5211cb690f31/elife-64904-fig1.jpg

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