Division of Cell Biology, Center for Anatomy and Cell Biology, Medical University of Vienna, Austria.
Department of Nanobiotechnology, Institute for Biophysics, University of Natural Resources and Life Sciences Vienna (BOKU), Austria.
FEBS J. 2022 Aug;289(15):4580-4601. doi: 10.1111/febs.16391. Epub 2022 Mar 9.
A-to-I RNA editing by ADARs is an abundant epitranscriptomic RNA-modification in metazoa. In mammals, Flna pre-mRNA harbours a single conserved A-to-I RNA editing site that introduces a Q-to-R amino acid change in Ig repeat 22 of the encoded protein. Previously, we showed that FLNA editing regulates smooth muscle contraction in the cardiovascular system and affects cardiac health. The present study investigates how ADAR2-mediated A-to-I RNA editing of Flna affects actin crosslinking, cell mechanics, cellular adhesion and cell migration. Cellular assays and AFM measurements demonstrate that the edited version of FLNA increases cellular stiffness and adhesion but impairs cell migration in both, mouse fibroblasts and human tumour cells. In vitro, edited FLNA leads to increased actin crosslinking, forming actin gels of higher stress resistance. Our study shows that Flna RNA editing is a novel regulator of cytoskeletal organisation, affecting the mechanical property and mechanotransduction of cells.
ADAR 介导的 A 到 I 的 RNA 编辑是后生动物中丰富的 RNA 表遗传修饰。在哺乳动物中,Flna 前体 mRNA 含有一个单一的保守的 A 到 I 的 RNA 编辑位点,该位点导致编码蛋白的 Ig 重复 22 中的 Q 到 R 的氨基酸变化。先前,我们表明,FLNA 的编辑调节心血管系统中的平滑肌收缩,并影响心脏健康。本研究调查 ADAR2 介导的 Flna 的 A 到 I 的 RNA 编辑如何影响肌动蛋白交联、细胞力学、细胞黏附和细胞迁移。细胞实验和原子力显微镜测量表明,FLNA 的编辑版本增加细胞硬度和黏附性,但损害了小鼠成纤维细胞和人肿瘤细胞的迁移能力。在体外,编辑后的 FLNA 导致肌动蛋白交联增加,形成具有更高抗张强度的肌动蛋白凝胶。我们的研究表明,Flna 的 RNA 编辑是细胞骨架组织的一种新的调节因子,影响细胞的机械特性和力学转导。