Unknown

Dataset Information

0

Functional regulation of FoxO1 in neural stem cell differentiation.


ABSTRACT: Forkhead transcription factor family O (FoxO) maintains adult stem cell reserves by supporting their long-term proliferative potential. MicroRNAs (miRs) regulate neuronal stem/progenitor cell (NSPC) proliferation and differentiation during neural development by controlling the expression of a specific set of target genes. In the neurogenic subventricular zone, FoxO1 is specifically expressed in NSPCs and is no longer detected during the transition to neuroblast stage, forming an inverse correlation with miR-9 expression. The 3'-untranslated region of FoxO1 contains a conserved target sequence of miR-9 and FoxO1 expression is coordinated in concert with miR-9 during neuronal differentiation. Our study demonstrates that FoxO1 contributes to NSPC fate decision through its cooperation with the Notch signaling pathway.

SUBMITTER: Kim DY 

PROVIDER: S-EPMC4816100 | biostudies-literature | 2015 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Functional regulation of FoxO1 in neural stem cell differentiation.

Kim D-Y DY   Hwang I I   Muller F L FL   Paik J-H JH  

Cell death and differentiation 20151016 12


Forkhead transcription factor family O (FoxO) maintains adult stem cell reserves by supporting their long-term proliferative potential. MicroRNAs (miRs) regulate neuronal stem/progenitor cell (NSPC) proliferation and differentiation during neural development by controlling the expression of a specific set of target genes. In the neurogenic subventricular zone, FoxO1 is specifically expressed in NSPCs and is no longer detected during the transition to neuroblast stage, forming an inverse correlat  ...[more]

Similar Datasets

| S-EPMC7475390 | biostudies-literature
| S-EPMC2867837 | biostudies-literature
| S-EPMC5285406 | biostudies-literature
| S-EPMC8155619 | biostudies-literature
| S-SCDT-EMBOR-2020-50283V1 | biostudies-other
| S-EPMC7645248 | biostudies-literature
| S-EPMC3184132 | biostudies-literature
| S-EPMC3153928 | biostudies-literature