ZFIN ID: ZDB-PUB-150905-4
Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor gene
Ishibashi, M., Manning, E., Shoubridge, C., Krecsmarik, M., Hawkins, T.A., Giacomotto, J., Zhao, T., Mueller, T., Bader, P.I., Cheung, S.W., Stankiewicz, P., Bain, N.L., Hackett, A., Reddy, C.C., Mechaly, A.S., Peers, B., Wilson, S.W., Lenhard, B., Bally-Cuif, L., Gecz, J., Becker, T.S., Rinkwitz, S.
Date: 2015
Source: Human genetics 134(11-12): 1163-82 (Journal)
Registered Authors: Bally-Cuif, Laure, Becker, Thomas S., Giacomotto, Jean, Hawkins, Tom, Ishibashi, Minaka, Mechaly, Alejandro, Mueller, Thomas, Peers, Bernard, Rinkwitz, Silke, Wilson, Steve, Zhao, Ting
Keywords: none
MeSH Terms:
  • Adult
  • Animals
  • Animals, Genetically Modified
  • Brain/embryology
  • Brain/metabolism
  • Case-Control Studies
  • DNA Copy Number Variations*
  • Embryo, Nonmammalian
  • Female
  • Gene Dosage
  • Gene Duplication*
  • Gene Expression Regulation, Developmental
  • Homeodomain Proteins/genetics*
  • Homeodomain Proteins/metabolism
  • Humans
  • Intellectual Disability/genetics*
  • Male
  • Transcription Factors/genetics*
  • Transcription Factors/metabolism
  • Zebrafish
PubMed: 26337422 Full text @ Hum. Genet.
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ABSTRACT
Protein-coding mutations in the transcription factor-encoding gene ARX cause various forms of intellectual disability (ID) and epilepsy. In contrast, variations in surrounding non-coding sequences are correlated with milder forms of non-syndromic ID and autism and had suggested the importance of ARX gene regulation in the etiology of these disorders. We compile data on several novel and some already identified patients with or without ID that carry duplications of ARX genomic region and consider likely genetic mechanisms underlying the neurodevelopmental defects. We establish the long-range regulatory domain of ARX and identify its brain region-specific autoregulation. We conclude that neurodevelopmental disturbances in the patients may not simply arise from increased dosage due to ARX duplication. This is further exemplified by a small duplication involving a non-functional ARX copy, but with duplicated enhancers. ARX enhancers are located within a 504-kb region and regulate expression specifically in the forebrain in developing and adult zebrafish. Transgenic enhancer-reporter lines were used as in vivo tools to delineate a brain region-specific negative and positive autoregulation of ARX. We find autorepression of ARX in the telencephalon and autoactivation in the ventral thalamus. Fluorescently labeled brain regions in the transgenic lines facilitated the identification of neuronal outgrowth and pathfinding disturbances in the ventral thalamus and telencephalon that occur when arxa dosage is diminished. In summary, we have established a model for how breakpoints in long-range gene regulation alter the expression levels of a target gene brain region-specifically, and how this can cause subtle neuronal phenotypes relating to the etiology of associated neuropsychiatric disease.
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