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NOTCH, a new signaling pathway implicated in holoprosencephaly.

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  • معلومة اضافية
    • Contributors:
      Institut de Génétique et Développement de Rennes (IGDR); Université de Rennes 1 (UR1); Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Centre National de la Recherche Scientifique (CNRS); Laboratoire de Génétique Moléculaire; Hôpital Pontchaillou; Service de génétique médicale; CHU Toulouse Toulouse -Hôpital Purpan Toulouse; CHU Toulouse Toulouse; Department of Clinical Genetics Churchill Hospital; Churchill Hospital Oxford Centre for Haematology; Centre de génétique - Centre de référence des maladies rares, anomalies du développement et syndromes malformatifs (CHU de Dijon); Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon); Department of Molecular and Human Genetics; Baylor College of Medicine (BCM); Baylor University-Baylor University; Service de génétique clinique; hôpital Sud
    • بيانات النشر:
      HAL CCSD
      Oxford University Press (OUP)
    • الموضوع:
      2011
    • Collection:
      Archive ouverte HAL (Hyper Article en Ligne, CCSD - Centre pour la Communication Scientifique Directe)
    • نبذة مختصرة :
      International audience ; Genetics of Holoprosencephaly (HPE), a congenital malformation of the developing human forebrain, is due to multiple genetic defects. Most genes that have been implicated in HPE belong to the sonic hedgehog signaling pathway. Here we describe a new candidate gene isolated from array comparative genomic hybridization redundant 6qter deletions, DELTA Like 1 (DLL1), which is a ligand of NOTCH. We show that DLL1 is co-expressed in the developing chick forebrain with Fgf8. By treating chick embryos with a pharmacological inhibitor, we demonstrate that DLL1 interacts with FGF signaling pathway. Moreover, a mutation analysis of DLL1 in HPE patients revealed a three-nucleotide deletion. These various findings implicate DLL1 in early patterning of the forebrain and identify NOTCH as a new signaling pathway involved in HPE.
    • Relation:
      info:eu-repo/semantics/altIdentifier/pmid/21196490; inserm-00554387; https://www.hal.inserm.fr/inserm-00554387; https://www.hal.inserm.fr/inserm-00554387/document; https://www.hal.inserm.fr/inserm-00554387/file/Dupe-2010-hum_mol_genet.pdf; https://www.hal.inserm.fr/inserm-00554387/file/inserm-00554387_edited.pdf; PUBMED: 21196490
    • الرقم المعرف:
      10.1093/hmg/ddq556
    • Rights:
      info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.7E138083