microRNA-124 directly suppresses Nodal and Notch to regulate mesodermal development
Kalin D Konrad1, Malcolm Arnott1, Michael Testa1
1Department of Biological Sciences, University of Delaware, Newark, DE 19716, USA.
MicroRNA-124 (miR-124) regulates sea urchin embryo development by controlling mesodermal cell differentiation. It represses Nodal and Notch signaling pathways, impacting blastocoelar cell and pigment cell fates.
Area of Science:
- Developmental Biology
- Molecular Biology
- Marine Biology
Background:
- MicroRNAs (miRNAs) are key post-transcriptional regulators of gene expression.
- MicroRNA-124 (miR-124) is primarily studied for its role in neurogenesis.
- The function of miR-124 in mesodermal cell differentiation remains largely unexplored.
Purpose of the Study:
- To investigate the novel role of miR-124 in regulating mesodermal cell differentiation in sea urchin embryos.
- To identify the downstream targets of miR-124 involved in cell fate decisions.
- To elucidate the impact of miR-124 on the development of blastocoelar cells (BCs) and pigment cells (PCs).
Main Methods:
- Expression analysis of miR-124 during sea urchin embryogenesis.
- Functional studies involving inhibition of miR-124 and its targets (Nodal, Notch).
- Analysis of cell differentiation markers for BCs and PCs using transcription factors (TFs).
Main Results:
- miR-124 expression begins at the early blastula stage, coinciding with endomesodermal specification.
- miR-124 directly represses Nodal and Notch signaling pathways.
- Inhibition of miR-124 leads to increased BCs and decreased PCs, while Notch inhibition results in increased BCs and PCs, including hybrid cells.
Conclusions:
- miR-124 plays a critical role in the binary fate decision between BCs and PCs in sea urchin embryos.
- Regulation of Nodal and Notch signaling pathways by miR-124 is essential for proper mesodermal cell differentiation.
- This study reveals a new function for miR-124 in regulating cell differentiation and proliferation via conserved signaling pathways.
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