The neural crest is a multipotent cell population that develops from the dorsal neural fold of vertebrate embryos in order to migrate extensively and differentiate into a variety of tissues. A number of gene regulatory networks coordinating neural crest cell specification and differentiation have been extensively studied to date. Although several publications suggest a common role for microRNA-145 (miR-145) in molecular reprogramming for cell cycle regulation and/or cellular differentiation, little is known about its role during in vivo cranial neural crest development. By modifying miR-145 levels in zebrafish embryos, abnormal craniofacial development and aberrant pigmentation phenotypes were detected. By whole-mount in situ hybridization, changes in expression patterns of and Sry-related HMG box (Sox) transcription factors and were observed in overexpressed miR-145 embryos. In agreement, zebrafish expression was downregulated by miR-145 overexpression. In silico and in vivo analysis of the 3'UTR revealed a conserved potential miR-145 binding site likely involved in its post-transcriptional regulation. Based on these findings, we speculate that miR-145 participates in the gene regulatory network governing zebrafish chondrocyte differentiation by controlling expression.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8306979 | PMC |
http://dx.doi.org/10.3390/genes12071023 | DOI Listing |
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