Cerebral cortical development is controlled by key transcription factors that specify the neuronal identities in the different layers. The mechanisms controlling their expression in distinct cells are only partially known. We investigated the expression and stability of Tbr1, Bcl11b, Fezf2, Satb2, and Cux1 mRNAs in single developing mouse cortical cells. We observe that Satb2 mRNA appears much earlier than its protein and in a set of cells broader than expected, suggesting an initial inhibition of its translation, subsequently released during development. Mechanistically, Satb2 30UTR modulates protein translation of GFP reporters during mouse corticogenesis. We select miR541, a eutherian-specific miRNA, and miR-92a/b as the best candidates responsible for SATB2 inhibition, being strongly expressed in early and reduced in late progenitor cells. Their inactivation triggers robust and premature SATB2 translation in both mouse and human cortical cells. Our findings indicate RNA interference as a major mechanism in timing cortical cell identities.

Martins, M., Galfrè, S., Terrigno, M., Pandolfini, L., Appolloni, I., Dunville, K., et al. (2021). A eutherian-specific microRNA controls the translation of Satb2 in a model of cortical differentiation. STEM CELL REPORTS, 16(6), 1496-1509 [10.1016/j.stemcr.2021.04.020].

A eutherian-specific microRNA controls the translation of Satb2 in a model of cortical differentiation

Pietrosanto, Marco;Helmer-Citterich, Manuela;
2021-01-01

Abstract

Cerebral cortical development is controlled by key transcription factors that specify the neuronal identities in the different layers. The mechanisms controlling their expression in distinct cells are only partially known. We investigated the expression and stability of Tbr1, Bcl11b, Fezf2, Satb2, and Cux1 mRNAs in single developing mouse cortical cells. We observe that Satb2 mRNA appears much earlier than its protein and in a set of cells broader than expected, suggesting an initial inhibition of its translation, subsequently released during development. Mechanistically, Satb2 30UTR modulates protein translation of GFP reporters during mouse corticogenesis. We select miR541, a eutherian-specific miRNA, and miR-92a/b as the best candidates responsible for SATB2 inhibition, being strongly expressed in early and reduced in late progenitor cells. Their inactivation triggers robust and premature SATB2 translation in both mouse and human cortical cells. Our findings indicate RNA interference as a major mechanism in timing cortical cell identities.
2021
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore BIO/11 - BIOLOGIA MOLECOLARE
English
Con Impact Factor ISI
SATB2
cell fate
cell identity
corpus callosum
cortex
cortical layering
developmental timing
in vitro corticogenesis
mammalian evolution
miR-catch
microRNA
neural stem cells
post-transcriptional control
3' Untranslated Regions
Animals
Cell Differentiation
Cell Line
Cerebral Cortex
Eutheria
Gene Expression Regulation, Developmental
Humans
Matrix Attachment Region Binding Proteins
Mice
MicroRNAs
Neurogenesis
Repressor Proteins
Transcription Factors
Tumor Suppressor Proteins
Martins, M., Galfrè, S., Terrigno, M., Pandolfini, L., Appolloni, I., Dunville, K., et al. (2021). A eutherian-specific microRNA controls the translation of Satb2 in a model of cortical differentiation. STEM CELL REPORTS, 16(6), 1496-1509 [10.1016/j.stemcr.2021.04.020].
Martins, M; Galfrè, S; Terrigno, M; Pandolfini, L; Appolloni, I; Dunville, K; Marranci, A; Rizzo, M; Mercatanti, A; Poliseno, L; Morandin, F; Pietros...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/292031
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