» Articles » PMID: 36823980

The Essential Function of MiR-5739 in Embryonic Muscle Development

Overview
Date 2023 Feb 24
PMID 36823980
Authors
Affiliations
Soon will be listed here.
Abstract

Background And Objectives: Embryologically, mesodermal development is closely related to the development of various organs such as muscles, blood vessels, and hearts, which are the main organs that make up the body. However, treatment for mesoderm developmental disorders caused by congenital or acquired factors has so far relied on surgery and drug treatment for symptom relief, and more fundamentally, treatment for mesoderm developmental disorders is needed.

Methods And Results: In our study, microRNA (miRNA), which plays an important role in the mesoderm development process, was identified and the developmental function was evaluated. miRNAs consist of small nucleotides, which act as transcription factors that bind to the 3' untranslated region and suppressed target gene expression. We constructed the human embryonic stem cell (hESC) knockout cell line and analyzed the function and characteristics of miR-5739, which plays an important role in mesoderm lineage. miR-5739 acts as a transcription factor targeting SMA, Brachyury T, Hand1, which controls muscle proliferation and differentiation, and KDR gene, which regulates vessel formation . results suggest a role in regulating muscle proliferation and differentiation. Gene ontology analysis confirmed that the miR-5739 is closely related to genes that regulate muscle and vessel proliferation and differentiation. Importantly, abnormal expression of miR-5739 was detected in somatic cells derived from patients with congenital muscle disease.

Conclusions: Our study demonstrate that miR-5739 gene function significantly affects transcriptional circuits that regulate muscle and vascular differentiation during embryonic development.

References
1.
Bindea G, Mlecnik B, Hackl H, Charoentong P, Tosolini M, Kirilovsky A . ClueGO: a Cytoscape plug-in to decipher functionally grouped gene ontology and pathway annotation networks. Bioinformatics. 2009; 25(8):1091-3. PMC: 2666812. DOI: 10.1093/bioinformatics/btp101. View

2.
Subramanyam D, Lamouille S, Judson R, Liu J, Bucay N, Derynck R . Multiple targets of miR-302 and miR-372 promote reprogramming of human fibroblasts to induced pluripotent stem cells. Nat Biotechnol. 2011; 29(5):443-8. PMC: 3685579. DOI: 10.1038/nbt.1862. View

3.
Yang H, Choi J, Kim H, Yang S, Park S, Kang C . Reconstituting Human Cutaneous Regeneration in Humanized Mice under Endothelial Cell Therapy. J Invest Dermatol. 2018; 139(3):692-701. DOI: 10.1016/j.jid.2018.08.031. View

4.
Park S, Lee J, Lee S, Lee J, Seo J, Choi J . Functional Equivalency in Human Somatic Cell Nuclear Transfer-Derived Endothelial Cells. Stem Cells. 2019; 37(5):623-630. DOI: 10.1002/stem.2986. View

5.
Han S, Shim H, Park S, Kim B, Lee D, Chung H . Safety and Optimization of Metabolic Labeling of Endothelial Progenitor Cells for Tracking. Sci Rep. 2018; 8(1):13212. PMC: 6123424. DOI: 10.1038/s41598-018-31594-0. View