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多能及分化中的NT2/D1细胞中PRMT6依赖性可变剪接的评估。

Assessment of PRMT6-dependent alternative splicing in pluripotent and differentiating NT2/D1 cells.

作者信息

Eudenbach Matthias, Busam Jonas, Bouchard Caroline, Rossbach Oliver, Zarnack Kathi, Bauer Uta-Maria

机构信息

Institute for Molecular Biology and Tumor Research (IMT), Philipps-University Marburg, Marburg, Germany.

Buchmann Institute for Molecular Life Sciences (BMLS) and Institute of Molecular Biosciences, Goethe University Frankfurt, Frankfurt, Germany.

出版信息

Life Sci Alliance. 2025 Feb 3;8(4). doi: 10.26508/lsa.202402946. Print 2025 Apr.

Abstract

Protein arginine methyltransferase 6 (PRMT6) is a well-characterized epigenetic regulator that methylates histone H3 at arginine 2 (H3R2me2a) in both promoter and enhancer regions, thereby modulating transcriptional initiation. We report here that PRMT6 also regulates gene expression at the post-transcriptional level in the neural pluripotent state and during neuronal differentiation of NT2/D1 cells. PRMT6 knockout causes widespread alternative splicing changes in NT2/D1 cells, most frequently cassette exon alterations. Most of the PRMT6-dependent splicing targets are not transcriptionally affected by the enzyme and regulated in an H3R2me2a-independent manner. However, for a small subset of splicing events, the PRMT6-mediated deposition of H3R2me2a overlaps with the splice site, suggesting a potential dual function in both transcriptional and co-/post-transcriptional regulation. The splicing targets of PRMT6 include ribosomal proteins, splicing factors, and chromatin-modifying enzymes such as PRMT4, DNMT3B, and ASH2L, some of which are associated with differentiation decisions. Taken together, our results in NT2/D1 cells show that PRMT6 exerts predominantly H3R2me2a-independent functions in RNA splicing, which may contribute to pluripotency and neuronal identity.

摘要

蛋白质精氨酸甲基转移酶6(PRMT6)是一种已被充分表征的表观遗传调节因子,它在启动子和增强子区域将组蛋白H3的精氨酸2位点甲基化(H3R2me2a),从而调节转录起始。我们在此报告,PRMT6在神经多能状态以及NT2/D1细胞的神经元分化过程中,也在转录后水平调节基因表达。PRMT6基因敲除导致NT2/D1细胞中广泛的可变剪接变化,最常见的是盒式外显子改变。大多数依赖PRMT6的剪接靶点不受该酶的转录影响,且以不依赖H3R2me2a的方式受到调控。然而,对于一小部分剪接事件,PRMT6介导的H3R2me2a沉积与剪接位点重叠,提示其在转录以及共转录/转录后调控中可能具有双重功能。PRMT6的剪接靶点包括核糖体蛋白、剪接因子以及染色质修饰酶,如PRMT4、DNMT3B和ASH2L,其中一些与分化决定相关。综上所述,我们在NT2/D1细胞中的研究结果表明,PRMT6在RNA剪接中主要发挥不依赖H3R2me2a的功能,这可能有助于多能性和神经元特性的维持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3fe/11791029/fbf9023792c8/LSA-2024-02946_GA.jpg

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