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MiRNA-128 regulates the proliferation and neurogenesis of neural precursors by targeting PCM1 in the developing cortex
Abstract
During the development, tight regulation of the expansion of neural progenitor cells (NPCs) and their differentiation into neurons is crucial for normal cortical formation and function. In this study, we demonstrate that microRNA (miR)-128 regulates the proliferation and differentiation of NPCs by repressing pericentriolar material 1 (PCM1). Specifically, overexpression of miR-128 reduced NPC proliferation but promoted NPC differentiation into neurons both in vivo and in vitro. In contrast, the reduction of endogenous miR-128 elicited the opposite effects. Overexpression of miR-128 suppressed the translation of PCM1, and knockdown of endogenous PCM1 phenocopied the observed effects of miR-128 overexpression. Furthermore, concomitant overexpression of PCM1 and miR-128 in NPCs rescued the phenotype associated with miR-128 overexpression, enhancing neurogenesis but inhibiting proliferation, both in vitro and in utero. Taken together, these results demonstrate a novel mechanism by which miR-128 regulates the proliferation and differentiation of NPCs in the developing neocortex.
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“while removal of miR-128-3p enhanced cell division, reducing neuron formation.33”
From MiR-128-3p – a gray eminence of the human central nervous system (2024) · cites this paper as [33]
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“miR-128-3p actively participates in embryonic brain development by regulating key genes, including PCM-1 (Pericentriolar material 1) and PHF6 (PHD finger protein 6) in neuronal progenitor cells.”
From MiR-128-3p – a gray eminence of the human central nervous system (2024) · cites this paper as [33]
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“This regulation promoted neurogenesis while inhibiting proliferation in the developing neocortex”
From MiR-128-3p – a gray eminence of the human central nervous system (2024) · cites this paper as [33]
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“Nuclei were counterstained with DAPI, and mitotic cells were immunostained with PH3.”
MethodInfluentialAdlakha, Y. K., & Saini, N. (2014) · Molecular Cancer · doi:10.1186/1476-4598-13-33 · Cited by 213
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Metadata
- Authors
- Zhang, W., Kim, P. J., Chen, Z., Lokman, H., Qiu, L., Zhang, K., Rozen, S. G., Tan, E. K., Je, H. S., & Zeng, L.
- Affiliations
- Neural Stem Cell Research Lab, Research Department, National Neuroscience Institute, Singapore, Singapore
- Molecular Neurophysiology Laboratory, Signature Program in Neuroscience and Behavioral Disorders, Duke-NUS Graduate Medical School, Singapore, Singapore
- Center for Computational Biology, Duke-NUS Graduate Medical School, Singapore, Singapore
- Department of Neurology, National Neuroscience Institute, Singapore, Singapore
- ORCID
- Je, Hyunsoo Shawn
- Venue
- eLife
- Publisher
- eLife Sciences Publications, Ltd
- Published
- 2016-02-17
- Volume
- 5
- ISSN
- 2050-084X
- PMC
- PMC4769165
- Cited by
- 71
- References
- 2
- Language
- en
- Licence
- Funders
- Singapore A*Star (13/1/96/19/688)
- Duke-NUS GMS Signature Research Program Grant
- NNI Research Grant
- Singapore Translational Research Investigator Award
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