| First Author | Chilov D | Year | 2011 |
| Journal | Dev Biol | Volume | 357 |
| Issue | 1 | Pages | 259-68 |
| PubMed ID | 21736876 | Mgi Jnum | J:175551 |
| Mgi Id | MGI:5286013 | Doi | 10.1016/j.ydbio.2011.06.029 |
| Citation | Chilov D, et al. (2011) Phosphorylated beta-catenin localizes to centrosomes of neuronal progenitors and is required for cell polarity and neurogenesis in developing midbrain. Dev Biol 357(1):259-68 |
| abstractText | beta-catenin has well-established functions in cell growth and differentiation as part of the Wnt signaling pathway and in regulation of cellular adhesion with E-cadherin. Here we studied its significance in midbrain development by temporally controlled deletion of beta-catenin allowing simultaneous analysis of complete (beta-cat-null) and partial (beta-cat-low) loss-of-function phenotypes in progenitor cells. beta-cat-null cells did not contain centrosomes or a microtubule network and were unpolarized forming delaminated bulges. beta-cat-low cells displayed defects in the orientation of the mitotic spindle, increased asymmetric cell divisions and premature differentiation in absence of alterations in polarity or adhesion. The spindle defect was associated with decreased centrosomal S33/S34/T41 phosphorylated beta-catenin (p-beta-cat) and centrosomal and microtubule defects. Interestingly, neural progenitor cells in mice expressing only unphosphorylatable beta-catenin share several phenotypes with beta-catenin loss-of-function mice with defects in microtubules and polarity. The results demonstrate a novel function for p-beta-cat in maintaining neuroepithelial integrity and suggest that centrosomal p-ss-cat is required to maintain symmetric cleavages and polarity in neural progenitors. |
