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Scientists find cause of facial widening defects

November 01, 2016

Widening across the forehead and nose occurs when loss of cilia at the surface of the cells disrupts internal signaling and causes two GLI proteins to stop repressing midfacial growth. Ching-Fang Chang and Samantha Brugmann of the Cincinnati Children's Hospital Medical Center in Ohio, US, report the findings in a study published November 1st, 2016 in PLOS Genetics.

Tiny projections, called cilia, are located on the surfaces of cells all over the body and serve an important role in cell signaling, which when lost, cause diverse diseases called ciliopathies. The midline of the face is especially susceptible to ciliopathies, and previous studies have shown that facial widening results from increases in Hedgehog signaling activity, a pathway that signals embryonic cells to direct development. However, the exact relationship between cilia loss and increased Hedgehog signaling is unclear. The scientists used mouse models of ciliopathies to investigate signaling proteins involved in this pathway, and looked specifically at the role of two proteins, GLI2 and GLI3. These proteins have both an activator form and a repressor form that regulate expression of genes in the Hedgehog pathway. When they disrupted signaling from the cilia, the mice experienced facial widening because the cells lost the repressor activity of GLI2 and GLI3 that normally keeps Hedgehog signaling in check.

The contributions of the activator and repressor functions of GLI genes to development is a complex topic that has been difficult for scientists to piece together. While the repressor forms of GLI3 and GLI2 were already known to play a role in neural tube and limb bud development, little was known about how these genes function in facial formation. These studies give insights into the mechanisms of how the cilia and GLI proteins function during midfacial development.
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In your coverage please use this URL to provide access to the freely available article in PLOS Genetics: http://dx.doi.org/10.1371/journal.pgen.1006351

Citation: Chang C-F, Chang Y-T, Millington G, Brugmann SA (2016) Craniofacial Ciliopathies Reveal Specific Requirements for GLI Proteins during Development of the Facial Midline. PLoS Genet 12(11): e1006351. doi:10.1371/journal.pgen.1006351

Funding: This work was supported by the National Institutes of Health (NIH)/National Institute of Dental and Craniofacial Research (NIDCR) grant R01DE023804 (SAB). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing Interests: The authors have declared that no competing interests exist.

PLOS

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