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.
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DOI:
10.1016/j.ydbio.2018.03.021
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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
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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
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.