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microRNA-mediated regulation of microRNA machinery controls cell fate decisions
- Source :
- eLife, eLife, Vol 10 (2021)
- Publication Year :
- 2021
- Publisher :
- eLife Sciences Publications, Ltd, 2021.
-
Abstract
- microRNAs associate with Argonaute proteins, forming the microRNA-induced silencing complex (miRISC), to repress target gene expression post-transcriptionally. Although microRNAs are critical regulators in mammalian cell differentiation, our understanding of how microRNA machinery, such as the miRISC, are regulated during development is still limited. We previously showed that repressing the production of one Argonaute protein, Ago2, by Trim71 is important for mouse embryonic stem cells (mESC) self-renewal (Liu et al., 2021). Here we show that among the four Argonaute proteins in mammals, Ago2 is the major developmentally regulated Argonaute protein in mESCs. Moreover, in pluripotency, besides the Trim71-mediated regulation of Ago2 (Liu et al., 2021), microRNA-182/microRNA-183 also repress Ago2. Specific inhibition of this microRNA-mediated repression results in stemness defects and accelerated differentiation through the let-7 microRNA pathway. These results reveal a microRNA-mediated regulatory circuit on microRNA machinery that is critical to maintaining pluripotency.
- Subjects :
- Ago2
Mouse
QH301-705.5
Science
Cell fate determination
Biology
General Biochemistry, Genetics and Molecular Biology
Cell Line
Mice
let-7 microrma
Mammalian cell
microRNA
Gene expression
Animals
Gene silencing
Cell Lineage
Biology (General)
Cell Self Renewal
Psychological repression
Cell Proliferation
General Immunology and Microbiology
General Neuroscience
RISC
Gene Expression Regulation, Developmental
Cell Differentiation
Mouse Embryonic Stem Cells
Cell Biology
mir-182
General Medicine
Argonaute
Chromosomes and Gene Expression
pluripotency
mir-183
Embryonic stem cell
Cell biology
MicroRNAs
Argonaute Proteins
Medicine
Regulatory circuit
Research Advance
Transcription Factors
Subjects
Details
- ISSN :
- 2050084X
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- eLife
- Accession number :
- edsair.doi.dedup.....19261b4fc0ec52a813eb7a1fda7769b5
- Full Text :
- https://doi.org/10.7554/elife.72289