Human Molecular Genetics, 2001, Vol. 10, No. 22 2593-2601
© 2001 Oxford University Press
Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification
Neural Development Unit, Institute of Child Health, University College London, 30 Guilford Street, London WC1N 1EH, UK and 1Department of Maternal and Fetal Medicine, Institute of Reproductive and Developmental Biology, Imperial College School of Medicine, Hammersmith Campus, London W12 0NN, UK
Neural tube defects (NTD) are clinically important congenital malformations whose molecular mechanisms are poorly understood. The loop-tail (Lp) mutant mouse provides a model for the most severe NTD, craniorachischisis, in which the brain and spinal cord remain open. During a positional cloning approach, we have identified a mutation in a novel gene, Lpp1, in the Lp mouse, providing a strong candidate for the genetic causation of craniorachischisis in Lp. Lpp1 encodes a protein of 521 amino acids, with four transmembrane domains related to the Drosophila protein strabismus/van gogh (vang). The human orthologue, LPP1, shares 89% identity with the mouse gene at the nucleotide level and 99% identity at the amino acid level. Lpp1 is expressed in the ventral part of the developing neural tube, but is excluded from the floor plate where Sonic hedgehog (Shh) is expressed. Embryos lacking Shh express Lpp1 throughout the ventral neural tube, suggesting negative regulation of Lpp1 by Shh. Our findings suggest that the mutual interaction between Lpp1 and Shh may define the lateral boundary of floor plate differentiation. Loss of Lpp1 function disrupts neurulation by permitting more extensive floor plate induction by Shh, thereby inhibiting midline bending of the neural plate during initiation of neurulation.
+ To whom correspondence should be addressed. Tel: +44 20 7829 8893; Fax: +44 20 7831 4366; Email: a.copp@ich.ucl.ac.uk The authors wish it to be known that, in their opinion, the first three authors should be regarded as joint First Authors
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
N. D.E. Greene, P. Stanier, and A. J. Copp Genetics of human neural tube defects Hum. Mol. Genet., October 15, 2009; 18(R2): R113 - R129. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. McNeill Planar Cell Polarity and the Kidney J. Am. Soc. Nephrol., October 1, 2009; 20(10): 2104 - 2111. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. W. Yen, M. Williams, A. Periasamy, M. Conaway, C. Burdsal, R. Keller, X. Lu, and A. Sutherland PTK7 is essential for polarized cell motility and convergent extension during mouse gastrulation Development, June 15, 2009; 136(12): 2039 - 2048. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. L. Patterson, C. Damrau, A. Paudyal, B. Reeve, D. T. Grimes, M. E. Stewart, D. J. Williams, P. Siggers, A. Greenfield, and J. N. Murdoch Mouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathway Hum. Mol. Genet., May 15, 2009; 18(10): 1719 - 1739. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. L. vandenBerg and D. A. Sassoon Non-canonical Wnt signaling regulates cell polarity in female reproductive tract development via van gogh-like 2 Development, May 1, 2009; 136(9): 1559 - 1570. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J. Garcia-Garcia, M. Shibata, and K. V. Anderson Chato, a KRAB zinc-finger protein, regulates convergent extension in the mouse embryo Development, September 15, 2008; 135(18): 3053 - 3062. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. M. Phillips, V. Hildreth, J. D. Peat, J. N. Murdoch, K. Kobayashi, B. Chaudhry, and D. J. Henderson Non-Cell-Autonomous Roles for the Planar Cell Polarity Gene Vangl2 in Development of the Coronary Circulation Circ. Res., March 14, 2008; 102(5): 615 - 623. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Torban, A.-M. Patenaude, S. Leclerc, S. Rakowiecki, S. Gauthier, G. Andelfinger, D. J. Epstein, and P. Gros Genetic interaction between members of the Vangl family causes neural tube defects in mice PNAS, March 4, 2008; 105(9): 3449 - 3454. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Kibar, E. Torban, J. R. McDearmid, A. Reynolds, J. Berghout, M. Mathieu, I. Kirillova, P. De Marco, E. Merello, J. M. Hayes, et al. Mutations in VANGL1 Associated with Neural-Tube Defects N. Engl. J. Med., April 5, 2007; 356(14): 1432 - 1437. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Wang and J. Nathans Tissue/planar cell polarity in vertebrates: new insights and new questions Development, February 15, 2007; 134(4): 647 - 658. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Ybot-Gonzalez, D. Savery, D. Gerrelli, M. Signore, C. E. Mitchell, C. H. Faux, N. D. E. Greene, and A. J. Copp Convergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closure Development, February 15, 2007; 134(4): 789 - 799. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. B. Wallingford Planar cell polarity, ciliogenesis and neural tube defects Hum. Mol. Genet., October 15, 2006; 15(suppl_2): R227 - R234. [Abstract] [Full Text] [PDF] |
||||
![]() |
M.-Y. Jung, L. Lorenz, and J. D. Richter Translational Control by Neuroguidin, a Eukaryotic Initiation Factor 4E and CPEB Binding Protein. Mol. Cell. Biol., June 1, 2006; 26(11): 4277 - 4287. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Wang, N. S. Hamblet, S. Mark, M. E. Dickinson, B. C. Brinkman, N. Segil, S. E. Fraser, P. Chen, J. B. Wallingford, and A. Wynshaw-Boris Dishevelled genes mediate a conserved mammalian PCP pathway to regulate convergent extension during neurulation Development, May 1, 2006; 133(9): 1767 - 1778. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Wang, N. Guo, and J. Nathans The role of Frizzled3 and Frizzled6 in neural tube closure and in the planar polarity of inner-ear sensory hair cells. J. Neurosci., February 22, 2006; 26(8): 2147 - 2156. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J.B. van den Hoff and A. F.M. Moorman Wnt, a Driver of Myocardialization? Circ. Res., February 18, 2005; 96(3): 274 - 276. [Full Text] [PDF] |
||||
![]() |
H. M. Phillips, J. N. Murdoch, B. Chaudhry, A. J. Copp, and D. J. Henderson Vangl2 Acts via RhoA Signaling to Regulate Polarized Cell Movements During Development of the Proximal Outflow Tract Circ. Res., February 18, 2005; 96(3): 292 - 299. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Torban, H.-J. Wang, N. Groulx, and P. Gros Independent Mutations in Mouse Vangl2 That Cause Neural Tube Defects in Looptail Mice Impair Interaction with Members of the Dishevelled Family J. Biol. Chem., December 10, 2004; 279(50): 52703 - 52713. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. F. Barald and M. W. Kelley From placode to polarization: new tunes in inner ear development Development, September 1, 2004; 131(17): 4119 - 4130. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Strutt Frizzled signalling and cell polarisation in Drosophila and vertebrates Development, October 1, 2003; 130(19): 4501 - 4513. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. B. Wallingford and R. M. Harland Neural tube closure requires Dishevelled-dependent convergent extension of the midline Development, March 14, 2003; 129(24): 5815 - 5825. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. S. Hamblet, N. Lijam, P. Ruiz-Lozano, J. Wang, Y. Yang, Z. Luo, L. Mei, K. R. Chien, D. J. Sussman, and A. Wynshaw-Boris Dishevelled 2 is essential for cardiac outflow tract development, somite segmentation and neural tube closure Development, March 14, 2003; 129(24): 5827 - 5838. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. N. Murdoch, D. J. Henderson, K. Doudney, C. Gaston-Massuet, H. M. Phillips, C. Paternotte, R. Arkell, P. Stanier, and A. J. Copp Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse Hum. Mol. Genet., January 15, 2003; 12(2): 87 - 98. [Abstract] [Full Text] [PDF] |
||||








