| Autor: |
Carpentieri, Jacopo A., Di Cicco, Amandine, Lampic, Marusa, Andreau, David, Del Maestro, Laurence, El Marjou, Fatima, Coquand, Laure, Bahi-Buisson, Nadia, Brault, Jean-Baptiste, Baffet, Alexandre D. |
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| Zdroj: |
Nature Communications; 10/23/2022, Vol. 13 Issue 1, p1-12, 12p |
| Abstrakt: |
Primary microcephaly and megalencephaly are severe brain malformations defined by reduced and increased brain size, respectively. Whether these two pathologies arise from related alterations at the molecular level is unclear. Microcephaly has been largely associated with centrosomal defects, leading to cell death. Here, we investigate the consequences of WDR81 loss of function, which causes severe microcephaly in patients. We show that WDR81 regulates endosomal trafficking of EGFR and that loss of function leads to reduced MAP kinase pathway activation. Mouse radial glial progenitor cells knocked-out for WDR81 exhibit reduced proliferation rate, subsequently leading to reduced brain size. These proliferation defects are rescued in vivo by expressing a megalencephaly-causing mutant form of Cyclin D2. Our results identify the endosomal machinery as an important regulator of proliferation rates and brain growth, demonstrating that microcephaly and megalencephaly can be caused by opposite effects on the proliferation rate of radial glial progenitors. Mutations in the human WDR81 gene result in severe microcephaly. Carpentieri et al. show that mutation of WDR81, a gene coding for an endosomal regulator, alters intracellular processing of the EGF receptor, leading to reduced proliferation rates of neuronal progenitors and to microcephaly. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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