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Mech Dev. 2012 Sep-Dec;129(9-12):308-23. doi: 10.1016/j.mod.2012.06.002. Epub 2012 Jun 15.

Delayed fusion and altered gene expression contribute to semicircular canal defects in Chd7 deficient mice.

Author information

1
Department of Pediatrics, The University of Michigan, Ann Arbor, MI 48109, USA.

Abstract

Proper morphogenesis of inner ear semicircular canals requires precise regulation of cellular proliferation, epithelial-to-mesenchymal transition, and fusion of epithelial plates. Epigenetic regulation of these processes is not well understood, but is likely to involve chromatin remodeling enzymes. CHD7 is a chromodomain-containing, ATP dependent helicase protein that is highly expressed in the developing ear and is required for semicircular canal development in both humans and mice. Here we report that mice with heterozygous loss of Chd7 function exhibit delayed semicircular canal genesis, delayed Netrin1 expression and disrupted expression of genes that are critical for semicircular canal formation (Bmp2, Bmp4, Msx1 and Fgf10). Complete loss of Chd7 results in aplasia of the semicircular canals and sensory vestibular organs, with reduced or absent expression of Otx1, Hmx3, Jagged1, Lmo4, Msx1 and Sox2. Our results suggest that Chd7 may have critical selector gene functions during inner ear morphogenesis. Detailed analysis of the epigenetic modifications underlying these gene expression changes should provide insights into semicircular canal development and help in the design of therapies for individuals with inner ear malformations.

PMID:
22705977
PMCID:
PMC3477510
DOI:
10.1016/j.mod.2012.06.002
[Indexed for MEDLINE]
Free PMC Article

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