FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation

Kimberly A. Aldinger, Ordan J. Lehmann, Louanne Hudgins, Viktor Chizhikov, Alexander G. Bassuk, Lesley C. Ades, Ian D. Krantz, William B. Dobyns, Kathleen J. Millen

Research output: Contribution to journalArticle

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Abstract

Dandy-Walker malformation (DWM), the most common human cerebellar malformation, has only one characterized associated locus. Here we characterize a second DWM-linked locus on 6p25.3, showing that deletions or duplications encompassing FOXC1 are associated with cerebellar and posterior fossa malformations including cerebellar vermis hypoplasia (CVH), mega-cisterna magna (MCM) and DWM. Foxc1-null mice have embryonic abnormalities of the rhombic lip due to loss of mesenchyme-secreted signaling molecules with subsequent loss of Atoh1 expression in vermis. Foxc1 homozygous hypomorphs have CVH with medial fusion and foliation defects. Human FOXC1 heterozygous mutations are known to affect eye development, causing a spectrum of glaucoma-associated anomalies (Axenfeld-Rieger syndrome, ARS; MIM no. 601631). We report the first brain imaging data from humans with FOXC1 mutations and show that these individuals also have CVH. We conclude that alteration of FOXC1 function alone causes CVH and contributes to MCM and DWM. Our results highlight a previously unrecognized role for mesenchyme-neuroepithelium interactions in the mid-hindbrain during early embryogenesis.

Original languageEnglish (US)
Pages (from-to)1037-1042
Number of pages6
JournalNature Genetics
Volume41
Issue number9
DOIs
StatePublished - Sep 1 2009

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Dandy-Walker Syndrome
Chromosomes
Cisterna Magna
Mesoderm
Rhombencephalon
Mutation
Lip
Neuroimaging
Glaucoma
Embryonic Development
Cerebellar Vermis
Cerebellar Hypoplasia

All Science Journal Classification (ASJC) codes

  • Genetics

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FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation. / Aldinger, Kimberly A.; Lehmann, Ordan J.; Hudgins, Louanne; Chizhikov, Viktor; Bassuk, Alexander G.; Ades, Lesley C.; Krantz, Ian D.; Dobyns, William B.; Millen, Kathleen J.

In: Nature Genetics, Vol. 41, No. 9, 01.09.2009, p. 1037-1042.

Research output: Contribution to journalArticle

Aldinger, KA, Lehmann, OJ, Hudgins, L, Chizhikov, V, Bassuk, AG, Ades, LC, Krantz, ID, Dobyns, WB & Millen, KJ 2009, 'FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation', Nature Genetics, vol. 41, no. 9, pp. 1037-1042. https://doi.org/10.1038/ng.422
Aldinger, Kimberly A. ; Lehmann, Ordan J. ; Hudgins, Louanne ; Chizhikov, Viktor ; Bassuk, Alexander G. ; Ades, Lesley C. ; Krantz, Ian D. ; Dobyns, William B. ; Millen, Kathleen J. / FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation. In: Nature Genetics. 2009 ; Vol. 41, No. 9. pp. 1037-1042.
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