Planar cell polarity signaling in craniofacial development

References

• Northcutt RG, Gans C. The genesis of neural crest and epidermal placodes: a reinterpretation of vertebrate origins. Q Rev Biol 1983; 58:1 - 28; PMID: 6346380; http://dx.doi.org/10.1086/413055
   PubMed Web of Science ®Google Scholar
• Schilling TF. Genetic analysis of craniofacial development in the vertebrate embryo. Bioessays 1997; 19:459 - 468; PMID: 9204763; http://dx.doi.org/10.1002/bies.950190605
   PubMed Web of Science ®Google Scholar
• Wansleeben C, Meijlink F. The planar cell polarity pathway in vertebrate development. Dev Dyn 2011; 240:616 - 626; PMID: 21305650; http://dx.doi.org/10.1002/dvdy.22564
   PubMed Web of Science ®Google Scholar
• Bekman E, Henrique D. Embryonic expression of three mouse genes with homology to the Drosophila melanogaster prickle gene. Mech Dev 2002; 119:77 - 81; PMID: 14516664; http://dx.doi.org/10.1016/S09254773(03)00095-9
   PubMed Web of Science ®Google Scholar
• Darken RS, Scola AM, Rakeman AS, Das G, Mlodzik M, Wilson PA. The planar polarity gene strabismus regulates convergent extension movements in Xenopus. EMBO J 2002; 21:976 - 985; PMID: 11867525; http://dx.doi.org/10.1093/emboj/21.5.976
   PubMed Web of Science ®Google Scholar
• Goto T, Keller R. The planar cell polarity gene strabismus regulates convergence and extension and neural fold closure in Xenopus. Dev Biol 2002; 247:165 - 181; PMID: 12074560; http://dx.doi.org/10.1006/dbio.2002.0673
   PubMed Web of Science ®Google Scholar
• Nakaya MA, Habas R, Biris K, Dunty WC Jr, Kato Y, He X, et al. Identification and comparative expression analyses of Daam genes in mouse and Xenopus. Gene Expr Patterns 2004; 5:97 - 105; PMID: 15533824; http://dx.doi.org/10.1016/j.modgep.2004.06.001
   PubMed Web of Science ®Google Scholar
• Carmona-Fontaine C, Matthews HK, Kuriyama S, Moreno M, Dunn GA, Parsons M, et al. Contact inhibition of locomotion in vivo controls neural crest directional migration. Nature 2008; 456:957 - 961; PMID: 19078960; http://dx.doi.org/10.1038/nature07441
   PubMed Web of Science ®Google Scholar
• De Calisto J, Araya C, Marchant L, Riaz CF, Mayor R. Essential role of non-canonical Wnt signalling in neural crest migration. Development 2005; 132:2587 - 2597; PMID: 15857909; http://dx.doi.org/10.1242/dev.01857
   PubMed Web of Science ®Google Scholar
• Clay MR, Halloran MC. Regulation of cell adhesions and motility during initiation of neural crest migration. Curr Opin Neurobiol 2011; 21:17 - 22; PMID: 20970990; http://dx.doi.org/10.1016/j.conb.2010.09.013
   PubMed Web of Science ®Google Scholar
• Matthews HK, Marchant L, Carmona-Fontaine C, Kuriyama S, Larrain J, Holt MR, et al. Directional migration of neural crest cells in vivo is regulated by Syndecan-4/Rac1 and non-canonical Wnt signaling/RhoA. Development 2008; 135:1771 - 1780; PMID: 18403410; http://dx.doi.org/10.1242/dev.017350
   PubMed Web of Science ®Google Scholar
• Shnitsar I, Borchers A. PTK7 recruits dsh to regulate neural crest migration. Development 2008; 135:4015 - 4024; PMID: 19004858; http://dx.doi.org/10.1242/dev.023556
   PubMed Web of Science ®Google Scholar
• Topczewski J, Sepich DS, Myers DC, Walker C, Amores A, Lele Z, et al. The zebrafish glypican knypek controls cell polarity during gastrulation movements of convergent extension. Dev Cell 2001; 1:251 - 264; PMID: 11702784; http://dx.doi.org/10.1016/S1534-5807(01)00005-3
   PubMed Web of Science ®Google Scholar
• LeClair EE, Mui SR, Huang A, Topczewska JM, Topczewski J. Craniofacial skeletal defects of adult zebrafish Glypican 4 (knypek) mutants. Dev Dyn 2009; 238:2550 - 2563; PMID: 19777561; http://dx.doi.org/10.1002/dvdy.22086
   PubMed Web of Science ®Google Scholar
• Person AD, Beiraghi S, Sieben CM, Hermanson S, Neumann AN, Robu ME, et al. WNT5A mutations in patients with autosomal dominant Robinow syndrome. Dev Dyn 2010; 239:327 - 337; PMID: 19918918; http://dx.doi.org/10.1002/dvdy.22156
   PubMed Web of Science ®Google Scholar
• Hartmann C. Skeletal development—Wnts are in control. Mol Cells 2007; 24:177 - 184; PMID: 17978569
   PubMed Web of Science ®Google Scholar
• Geetha-Loganathan P, Nimmagadda S, Antoni L, Fu K, Whiting CJ, Francis-West P, et al. Expression of WNT signalling pathway genes during chicken craniofacial development. Dev Dyn 2009; 238:1150 - 1165; PMID: 19334275; http://dx.doi.org/10.1002/dvdy.21934
   PubMed Web of Science ®Google Scholar
• Witte F, Dokas J, Neuendorf F, Mundlos S, Stricker S. Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation. Gene Expr Patterns 2009; 9:215 - 223; PMID: 19185060; http://dx.doi.org/10.1016/j.gep.2008.12.009
   PubMed Web of Science ®Google Scholar
• Yamaguchi TP, Bradley A, McMahon AP, Jones SA. Wnt5a pathway underlies outgrowth of multiple structures in the vertebrate embryo. Development 1999; 126:1211 - 1223; PMID: 10021340
   PubMed Web of Science ®Google Scholar
• Dale RM, Sisson BE, Topczewski J. The emerging role of Wnt/PCP signaling in organ formation. Zebrafish 2009; 6:9 - 14; PMID: 19250029; http://dx.doi.org/10.1089/zeb.2008.0563
   PubMed Web of Science ®Google Scholar
• Piotrowski T, Schilling TF, Brand M, Jiang YJ, Heisenberg CP, Beuchle D, et al. Jaw and branchial arch mutants in zebrafish II: anterior arches and cartilage differentiation. Development 1996; 123:345 - 356; PMID: 9007254
   PubMed Web of Science ®Google Scholar
• Ryu JH, Chun JS. Opposing roles of WNT-5A and WNT-11 in interleukin-1beta regulation of type II collagen expression in articular chondrocytes. J Biol Chem 2006; 281:22039 - 22047; PMID: 16754689; http://dx.doi.org/10.1074/jbc.M601804200
   PubMed Web of Science ®Google Scholar
• Yang Y, Topol L, Lee H, Wu J. Wnt5a and Wnt5b exhibit distinct activities in coordinating chondrocyte proliferation and differentiation. Development 2003; 130:1003 - 1015; PMID: 12538525; http://dx.doi.org/10.1242/dev.00324
   PubMed Web of Science ®Google Scholar
• Gao B, Song H, Bishop K, Elliot G, Garrett L, English MA, et al. Wnt signaling gradients establish planar cell polarity by inducing Vangl2 phosphorylation through Ror2. Dev Cell 2011; 20:163 - 176; PMID: 21316585; http://dx.doi.org/10.1016/j.devcel.2011.01.001
   PubMed Web of Science ®Google Scholar
• Oishi I, Suzuki H, Onishi N, Takada R, Kani S, Ohkawara B, et al. The receptor tyrosine kinase Ror2 is involved in non-canonical Wnt5a/JNK signalling pathway. Genes Cells 2003; 8:645 - 654; PMID: 12839624; http://dx.doi.org/10.1046/j.1365-2443.2003.00662.x
   PubMed Web of Science ®Google Scholar
• Yoda A, Oishi I, Minami Y. Expression and function of the Ror-family receptor tyrosine kinases during development: lessons from genetic analyses of nematodes, mice and humans. J Recept Signal Transduct Res 2003; 23:1 - 15; PMID: 12680586; http://dx.doi.org/10.1081/RRS-120018757
   PubMed Web of Science ®Google Scholar
• Lin M, Li L, Liu C, Liu H, He F, Yan F, et al. Wnt5a regulates growth, patterning, and odontoblast differentiation of developing mouse tooth. Dev Dyn 2011; 240:432 - 440; PMID: 21246660; http://dx.doi.org/10.1002/dvdy.22550
   PubMed Web of Science ®Google Scholar
• DeChiara TM, Kimble RB, Poueymirou WT, Rojas J, Masiakowski P, Valenzuela DM, et al. Ror2, encoding a receptor-like tyrosine kinase, is required for cartilage and growth plate development. Nat Genet 2000; 24:271 - 274; PMID: 10700181; http://dx.doi.org/10.1038/73488
   PubMed Web of Science ®Google Scholar
• Schwabe GC, Trepczik B, Suring K, Brieske N, Tucker AS, Sharpe PT, et al. Ror2 knockout mouse as a model for the developmental pathology of autosomal recessive Robinow syndrome. Dev Dyn 2004; 229:400 - 410; PMID: 14745966; http://dx.doi.org/10.1002/dvdy.10466
   PubMed Web of Science ®Google Scholar
• Takeuchi S, Takeda K, Oishi I, Nomi M, Ikeya M, Itoh K, et al. Mouse Ror2 receptor tyrosine kinase is required for the heart development and limb formation. Genes Cells 2000; 5:71 - 78; PMID: 10651906; http://dx.doi.org/10.1046/j.1365-2443.2000.00300.x
   PubMed Web of Science ®Google Scholar
• van Bokhoven H, Celli J, Kayserili H, van Beusekom E, Balci S, Brussel W, et al. Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome. Nat Genet 2000; 25:423 - 426; PMID: 10932187; http://dx.doi.org/10.1038/78113
   PubMed Web of Science ®Google Scholar
• Wang B, Sinha T, Jiao K, Serra R, Wang J. Disruption of PCP signaling causes limb morphogenesis and skeletal defects and may underlie Robinow syndrome and brachydactyly type B. Hum Mol Genet 2011; 20:271 - 285; PMID: 20962035; http://dx.doi.org/10.1093/hmg/ddq462
   PubMed Web of Science ®Google Scholar
• Robinow M, Silverman FN, Smith HD. A newly recognized dwarfing syndrome. Am J Dis Child 1969; 117:645 - 651; PMID: 5771504
   PubMedGoogle Scholar
• Afzal AR, Jeffery S. One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B. Hum Mutat 2003; 22:1 - 11; PMID: 12815588; http://dx.doi.org/10.1002/humu.10233
   PubMed Web of Science ®Google Scholar
• Oldridge M, Fortuna AM, Maringa M, Propping P, Mansour S, Pollitt C, et al. Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B. Nat Genet 2000; 24:275 - 278; PMID: 10700182; http://dx.doi.org/10.1038/73495
   PubMed Web of Science ®Google Scholar
• Fico A, Maina F, Dono R. Fine-tuning of cell signaling by glypicans. Cell Mol Life Sci 2011; 68:923 - 929; PMID: 18087675; http://dx.doi.org/10.1007/s00018-007-7471-6
   PubMed Web of Science ®Google Scholar
• Filmus J, Capurro M, Rast J. Glypicans. Genome Biol 2008; 9:224; PMID: 18505598; http://dx.doi.org/10.1186/gb-2008-9-5-224
   PubMed Web of Science ®Google Scholar
• Solnica-Krezel L, Stemple DL, Mountcastle-Shah E, Rangini Z, Neuhauss SC, Malicki J, et al. Mutations affecting cell fates and cellular rearrangements during gastrulation in zebrafish. Development 1996; 123:67 - 80; PMID: 9007230
   PubMed Web of Science ®Google Scholar
• Clément A, Wiweger M, von der Hardt S, Rusch MA, Selleck SB, Chien CB, et al. Regulation of zebrafish skeletogenesis by ext2/dackel and papst1/pinscher. PLoS Genet 2008; 4:1000136; PMID: 18654627; http://dx.doi.org/10.1371/journal.pgen.1000136
   PubMed Web of Science ®Google Scholar
• Ahn J, Ludecke HJ, Lindow S, Horton WA, Lee B, Wagner MJ, et al. Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1). Nat Genet 1995; 11:137 - 143; PMID: 7550340; http://dx.doi.org/10.1038/ng1095-137
   PubMed Web of Science ®Google Scholar
• Wuyts W, Van Hul W, Wauters J, Nemtsova M, Reyniers E, Van Hul EV, et al. Positional cloning of a gene involved in hereditary multiple exostoses. Hum Mol Genet 1996; 5:1547 - 1557; PMID: 8894688; http://dx.doi.org/10.1093/hmg/5.10.1547
   PubMed Web of Science ®Google Scholar
• Zak BM, Crawford BE, Esko JD. Hereditary multiple exostoses and heparan sulfate polymerization. Biochim Biophys Acta 2002; 1573:346 - 355; PMID: 12417417; http://dx.doi.org/10.1016/S0304-4165(02)00402-6
   PubMed Web of Science ®Google Scholar
• Koziel L, Kunath M, Kelly OG, Vortkamp A. Ext1-dependent heparan sulfate regulates the range of Ihh signaling during endochondral ossification. Dev Cell 2004; 6:801 - 813; PMID: 15177029; http://dx.doi.org/10.1016/j.devcel.2004.05.009
   PubMed Web of Science ®Google Scholar
• Kazanskaya O, Glinka A, del Barco Barrantes I, Stannek P, Niehrs C, Wu W. R-Spondin2 is a secreted activator of Wnt/beta-catenin signaling and is required for Xenopus myogenesis. Dev Cell 2004; 7:525 - 534; PMID: 15469841; http://dx.doi.org/10.1016/j.devcel.2004.07.019
   PubMed Web of Science ®Google Scholar
• Kim KA, Wagle M, Tran K, Zhan X, Dixon MA, Liu S, et al. R-Spondin family members regulate the Wnt pathway by a common mechanism. Mol Biol Cell 2008; 19:2588 - 2596; PMID: 18400942; http://dx.doi.org/10.1091/mbc.E08-02-0187
   PubMed Web of Science ®Google Scholar
• Ohkawara B, Glinka A, Niehrs C. Rspo3 binds syndecan 4 and induces Wnt/PCP signaling via clathrin-mediated endocytosis to promote morphogenesis. Dev Cell 2011; 20:303 - 314; PMID: 21397842; http://dx.doi.org/10.1016/j.devcel.2011.01.006
   PubMed Web of Science ®Google Scholar
• Lang MR, Lapierre LA, Frotscher M, Goldenring JR, Knapik EW. Secretory COPII coat component Sec23a is essential for craniofacial chondrocyte maturation. Nat Genet 2006; 38:1198 - 1203; PMID: 16980978; http://dx.doi.org/10.1038/ng1880
   PubMed Web of Science ®Google Scholar
• Ohisa S, Inohaya K, Takano Y, Kudo A. sec24d encoding a component of COPII is essential for vertebra formation, revealed by the analysis of the medaka mutant, vbi. Dev Biol 2010; 342:85 - 95; PMID: 20346938; http://dx.doi.org/10.1016/j.ydbio.2010.03.016
   PubMed Web of Science ®Google Scholar
• Sarmah S, Barrallo-Gimeno A, Melville DB, Topczewski J, Solnica-Krezel L, Knapik EW. Sec24D-dependent transport of extracellular matrix proteins is required for zebrafish skeletal morphogenesis. PLoS ONE 2010; 5:10367; PMID: 20442775; http://dx.doi.org/10.1371/journal.pone.0010367
   PubMed Web of Science ®Google Scholar
• Hicke L, Schekman R. Yeast Sec23p acts in the cytoplasm to promote protein transport from the endoplasmic reticulum to the Golgi complex in vivo and in vitro. EMBO J 1989; 8:1677 - 1684; PMID: 2670558
   PubMed Web of Science ®Google Scholar
• Yoshihisa T, Barlowe C, Schekman R. Requirement for a GTPase-activating protein in vesicle budding from the endoplasmic reticulum. Science 1993; 259:1466 - 1468; PMID: 8451644; http://dx.doi.org/10.1126/science.8451644
   PubMed Web of Science ®Google Scholar
• Wendeler MW, Paccaud JP, Hauri HP. Role of Sec24 isoforms in selective export of membrane proteins from the endoplasmic reticulum. EMBO Rep 2007; 8:258 - 264; PMID: 17255961; http://dx.doi.org/10.1038/sj.embor.7400893
   PubMed Web of Science ®Google Scholar
• Merte J, Jensen D, Wright K, Sarsfield S, Wang Y, Schekman R, et al. Sec24b selectively sorts Vangl2 to regulate planar cell polarity during neural tube closure. Nat Cell Biol 2010; 12:41 - 46; PMID: 19966784; http://dx.doi.org/10.1038/ncb2002
   PubMed Web of Science ®Google Scholar
• Wansleeben C, Feitsma H, Montcouquiol M, Kroon C, Cuppen E, Meijlink F. Planar cell polarity defects and defective Vangl2 trafficking in mutants for the COPII gene Sec24b. Development 2010; 137:1067 - 1073; PMID: 20215345; http://dx.doi.org/10.1242/dev.041434
   PubMed Web of Science ®Google Scholar
• Boyadjiev SA, Justice CM, Eyaid W, McKusick VA, Lachman RS, Chowdry AB, et al. A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21. Hum Genet 2003; 113:1 - 9; PMID: 12677423; http://dx.doi.org/10.1007/s00439-003-0932-6
   PubMed Web of Science ®Google Scholar
• Greene RM, Pisano MM. Palate morphogenesis: Current understanding and future directions. Birth Defects Res C Embryo Today 2010; 90:133 - 154; PMID: 20544696; http://dx.doi.org/10.1002/bdrc.20180
   PubMed Web of Science ®Google Scholar
• Niemann S, Zhao C, Pascu F, Stahl U, Aulepp U, Niswander L, et al. Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family. Am J Hum Genet 2004; 74:558 - 563; PMID: 14872406; http://dx.doi.org/10.1086/382196
   PubMed Web of Science ®Google Scholar
• Juriloff DM, Harris MJ, McMahon AP, Carroll TJ, Lidral AC. Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test. Birth Defects Res A Clin Mol Teratol 2006; 76:574 - 579; PMID: 16998816; http://dx.doi.org/10.1002/bdra.20302
   PubMed Web of Science ®Google Scholar
• Lee JM, Kim JY, Cho KW, Lee MJ, Cho SW, Kwak S, et al. Wnt11/Fgfr1b cross-talk modulates the fate of cells in palate development. Dev Biol 2008; 314:341 - 350; PMID: 18191119; http://dx.doi.org/10.1016/j.ydbio.2007.11.033
   PubMed Web of Science ®Google Scholar
• He F, Xiong W, Yu X, Espinoza-Lewis R, Liu C, Gu S, et al. Wnt5a regulates directional cell migration and cell proliferation via Ror2-mediated noncanonical pathway in mammalian palate development. Development 2008; 135:3871 - 3879; PMID: 18948417; http://dx.doi.org/10.1242/dev.025767
   PubMed Web of Science ®Google Scholar
• Yu H, Smallwood PM, Wang Y, Vidaltamayo R, Reed R, Nathans J. Frizzled 1 and frizzled 2 genes function in palate, ventricular septum and neural tube closure: general implications for tissue fusion processes. Development 2010; 137:3707 - 3717; PMID: 20940229; http://dx.doi.org/10.1242/dev.052001
   PubMed Web of Science ®Google Scholar
• Kibar Z, Vogan KJ, Groulx N, Justice MJ, Underhill DA, Gros P. Ltap, a mammalian homolog of Drosophila Strabismus/Van Gogh, is altered in the mouse neural tube mutant Loop-tail. Nat Genet 2001; 28:251 - 255; PMID: 11431695; http://dx.doi.org/10.1038/90081
   PubMed Web of Science ®Google Scholar
• Montcouquiol M, Rachel RA, Lanford PJ, Copeland NG, Jenkins NA, Kelley MW. Identification of Vangl2 and Scrb1 as planar polarity genes in mammals. Nature 2003; 423:173 - 177; PMID: 12724779; http://dx.doi.org/10.1038/nature01618
   PubMed Web of Science ®Google Scholar
• Murdoch JN, Doudney K, Paternotte C, Copp AJ, Stanier P. Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification. Hum Mol Genet 2001; 10:2593 - 2601; PMID: 11709546; http://dx.doi.org/10.1093/hmg/10.22.2593
   PubMed Web of Science ®Google Scholar