Planar cell polarity (PCP) signalling is vital for initiation of mouse neurulation, with diminished convergent extension (CE) cell movements leading to craniorachischisis, a severe neural tube defect (NTD). Some humans with NTDs also have PCP gene mutations but these are heterozygous, not homozygous as in mice. Other genetic or environmental factors may interact with partial loss of PCP function in human NTDs. We found that reduced sulfation of glycosaminoglycans interacts with heterozygosity for the Lp allele of Vangl2 (a core PCP gene), to cause craniorachischisis in cultured mouse embryos, with rescue by exogenous sulphate. We hypothesised this glycosaminoglycan-PCP interaction may regulate CE but, surprisingly, DiO labeling of the embryonic node demonstrates no abnormality of midline axial extension in sulfation-depleted Lp/+ embryos. Positive-control Lp/Lp embryos show severe CE defects. Abnormalities were detected in the size and shape of somites that flank the closing neural tube in sulfation-depleted Lp/+ embryos. We conclude that failure of closure initiation can arise by a mechanism other than faulty neuroepithelial CE, with possible involvement of matrix-mediated somite expansion, adjacent to the closing neural tube.
Vangl2-environment interaction causes severe neural tube defects, without abnormal neuroepithelial convergent extension
Present addresses: Neuro-endocrinology/Nutrition, Food Bioscience Department, Teagasc Moorepark, Fermoy, Co. Cork, Ireland
Present addresses: Epigenetics Programme, The Babraham Institute, Cambridge, UK
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- Funder(s): Wellcome
- Award Id(s): 0875525
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Oleksandr Nychyk, Gabriel L. Galea, Matteo Molè, Dawn Savery, Nicholas D.E. Greene, Philip Stanier, Andrew J. Copp; Vangl2-environment interaction causes severe neural tube defects, without abnormal neuroepithelial convergent extension. Dis Model Mech 2021; dmm.049194. doi: https://doi.org/10.1242/dmm.049194
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