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Planar cell polarity breaks bilateral symmetry by controlling ciliary positioning.

Defining the three body axes is a central event of vertebrate morphogenesis. Establishment of left-right (L-R) asymmetry in development follows the determination of dorsal-ventral and anterior-posterior (A-P) body axes, although the molecular mechanism underlying precise L-R symmetry breaking in reference to the other two axes is still poorly understood. Here, by removing both Vangl1 and Vangl2, the two mouse homologues of a Drosophila core planar cell polarity (PCP) gene Van Gogh (Vang), we reveal a previously unrecognized function of PCP in the initial breaking of lateral symmetry. The leftward nodal flow across the posterior notochord (PNC) has been identified as the earliest event in the de novo formation of L-R asymmetry. We show that PCP is essential in interpreting the A-P patterning information and linking it to L-R asymmetry. In the absence of Vangl1 and Vangl2, cilia are positioned randomly around the centre of the PNC cells and nodal flow is turbulent, which results in disrupted L-R asymmetry. PCP in mouse, unlike what has been implicated in other vertebrate species, is not required for ciliogenesis, cilium motility, Sonic hedgehog (Shh) signalling or apical docking of basal bodies in ciliated tracheal epithelial cells. Our data suggest that PCP acts earlier than the unidirectional nodal flow during bilateral symmetry breaking in vertebrates and provide insight into the functional mechanism of PCP in organizing the vertebrate tissues in development.

Pubmed ID: 20562861


  • Song H
  • Hu J
  • Chen W
  • Elliott G
  • Andre P
  • Gao B
  • Yang Y



Publication Data

July 15, 2010

Associated Grants

  • Agency: Intramural NIH HHS, Id: ZIA HG000187-09

Mesh Terms

  • Alleles
  • Animals
  • Body Patterning
  • Carrier Proteins
  • Cell Polarity
  • Cilia
  • Embryo, Mammalian
  • Functional Laterality
  • Membrane Proteins
  • Mice
  • Nerve Tissue Proteins