دورية أكاديمية

Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development.

التفاصيل البيبلوغرافية
العنوان: Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development.
المؤلفون: Cappello, S., Gray, M.J., Badouel, C., Lange, S., Einsiedler, M., Srour, M., Chitayat, D., Hamdan, F.F., Jenkins, Z.A., Morgan, T., Preitner, N., Uster, T., Thomas, J., Shannon, P., Morrison, V., di Donato, N., van Maldergem, L., Neuhann, T., Newbury-Ecob, R., Swinkells, M., Terhal, P., Wilson, L.C., Zwijnenburg, P.J., Sutherland-Smith, A.J., Black, M.A., Markie, D., Michaud, J.L., Simpson, M.A., Mansour, S., McNeill, H., Götz, M., Robertson, S.P.
المصدر: Nat. Genet. 45, 1300-1308 (2013)
بيانات النشر: Nature Publishing
سنة النشر: 2013
المجموعة: PuSH - Publikationsserver des Helmholtz Zentrums München
الوصف: The regulated proliferation and differentiation of neural stem cells before the generation and migration of neurons in the cerebral cortex are central aspects of mammalian development. Periventricular neuronal heterotopia, a specific form of mislocalization of cortical neurons, can arise from neuronal progenitors that fail to negotiate aspects of these developmental processes. Here we show that mutations in genes encoding the receptor-ligand cadherin pair DCHS1 and FAT4 lead to a recessive syndrome in humans that includes periventricular neuronal heterotopia. Reducing the expression of Dchs1 or Fat4 within mouse embryonic neuroepithelium increased progenitor cell numbers and reduced their differentiation into neurons, resulting in the heterotopic accumulation of cells below the neuronal layers in the neocortex, reminiscent of the human phenotype. These effects were countered by concurrent knockdown of Yap, a transcriptional effector of the Hippo signaling pathway. These findings implicate Dchs1 and Fat4 upstream of Yap as key regulators of mammalian neurogenesis.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 1061-4036
1546-1718
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/24056717; info:eu-repo/semantics/altIdentifier/wos/WOS:000326384100010; info:eu-repo/semantics/altIdentifier/isbn/1061-4036; info:eu-repo/semantics/altIdentif; https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=27509Test; urn:isbn:1061-4036; urn:issn:1061-4036; urn:issn:1546-1718
DOI: 10.1038/ng.2765
الإتاحة: https://doi.org/10.1038/ng.2765Test
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=27509Test
حقوق: info:eu-repo/semantics/closedAccess
رقم الانضمام: edsbas.63AD27A5
قاعدة البيانات: BASE
الوصف
تدمد:10614036
15461718
DOI:10.1038/ng.2765