miR-206 is required for changes in cell adhesion that drive muscle cell morphogenesis in Xenopus laevis.

miR-206 is required for changes in cell adhesion that drive muscle cell morphogenesis in Xenopus laevis.
复制标题

DOI:
10.1016/j.ydbio.2018.03.021
复制
发表时间:
2018-06
影响因子:
2.7
通讯作者:
H. Vergara;Julio Ramirez;Trista Rosing;Ceazar Nave;R. Blandino;D. Saw;Parag Saraf;Gabriel Piexoto;Coohleen Coombes;M. Adams;C. Domingo
H. Vergara;Julio Ramirez;Trista Rosing;Ceazar Nave;R. Blandino;D. Saw;Parag Saraf;Gabriel Piexoto;Coohleen Coombes;M. Adams;C. Domingo
中科院分区:
生物学3区
文献类型:
--
作者:
H. Vergara;Julio Ramirez;Trista Rosing;Ceazar Nave;R. Blandino;D. Saw;Parag Saraf;Gabriel Piexoto;Coohleen Coombes;M. Adams;C. Domingo

文献摘要

被引文献

相似文献

MicroRNAs (miRNAs)是高度保守的非编码小RNA分子,在多细胞生物中转录后调节基因表达。在一组肌肉特异性mirna中,miR-206的表达主要局限于骨骼肌,并且仅在硬骨鱼谱系中发现。尽管许多研究表明miR-206与肌肉维持和疾病有关,但其在骨骼肌发育中的作用在很大程度上仍然未知。在这里,我们研究了miR-206在非洲爪蟾体细胞发生中的作用。在非洲爪蟾中,miR-206的表达与躯体发生的开始一致。我们发现miR-206的敲低和过表达都会导致异常体形成,影响肌肉细胞的旋转、附着和伸长。特别是,我们的数据表明,miR-206调节细胞粘附的变化,影响新形成的体粘附脊索和体间边界的能力。此外,我们发现β-三磷酸糖酐和f -肌动蛋白的表达水平显著降低,这表明miR-206水平的下调影响了细胞形状变化和附着所需的细胞力学,而这些是适当肌肉形成所必需的。
MicroRNAs (miRNAs) are highly conserved small non-coding RNA molecules that post-transcriptionally regulate gene expression in multicellular organisms. Within the set of muscle-specific miRNAs, miR-206 expression is largely restricted to skeletal muscle and is found exclusively within the bony fish lineage. Although many studies have implicated miR-206 in muscle maintenance and disease, its role in skeletal muscle development remains largely unknown. Here, we examine the role of miR-206 duringXenopus laevissomitogenesis. InXenopus laevis,miR-206 expression coincides with the onset of somitogenesis. We show that both knockdown and over-expression of miR-206 result in abnormal somite formation affecting muscle cell rotation, attachment, and elongation. In particular, our data suggests that miR-206 regulates changes in cell adhesion that affect the ability of newly formed somites to adhere to the notochord as well as to the intersomitic boundaries. Additionally, we show that β-dystroglycan and F-actin expression levels are significantly reduced, suggesting that knockdown of miR-206 levels affects cellular mechanics necessary for cell shape changes and attachments that are required for proper muscle formation.