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Addendum

Pigmentation-based insertional mutagenesis is a simple and potent screening approach for identifying neurocristopathy-associated genes in mice

Article: e1156287 | Received 17 Dec 2015, Accepted 12 Feb 2016, Published online: 06 Apr 2016

References

  • Bronner ME, LeDouarin NM. Development and evolution of the neural crest: an overview. Dev Biol 2012; 366:2-9; PMID:22230617; http://dx.doi.org/10.1016/j.ydbio.2011.12.042
  • Bolande RP. Neurocristopathy: its growth and development in 20 years. Pediatr Pathol Lab Med 1997; 17:1-25; PMID:9050057; http://dx.doi.org/10.1080/15513819709168343
  • Etchevers HC, Amiel J, Lyonnet S. Molecular bases of human neurocristopathies. Adv Exp Med Biol 2006; 589:213-34; PMID:17076285; http://dx.doi.org/10.1007/978-0-387-46954-6_14
  • Bergeron KF, Cardinal T, Toure AM, Beland M, Raiwet DL, Silversides DW, Pilon N. Male-biased aganglionic megacolon in the TashT mouse line due to perturbation of silencer elements in a large gene desert of chromosome 10. PLoS Genet 2015; 11:e1005093; PMID:25786024; http://dx.doi.org/10.1371/journal.pgen.1005093
  • Soret R, Mennetrey M, Bergeron KF, Dariel A, Neunlist M, Grunder F, Faure C, Silversides DW, Pilon N. A collagen VI-dependent pathogenic mechanism for Hirschsprung's disease. J Clin Invest 2015; 125:4483-96; PMID:26571399; http://dx.doi.org/10.1172/JCI83178
  • Yokoyama T, Silversides DW, Waymire KG, Kwon BS, Takeuchi T, Overbeek PA. Conserved cysteine to serine mutation in tyrosinase is responsible for the classical albino mutation in laboratory mice. Nucleic Acids Res 1990; 18:7293-8; PMID:2124349; http://dx.doi.org/10.1093/nar/18.24.7293
  • Methot D, Reudelhuber TL, Silversides DW. Evaluation of tyrosinase minigene co-injection as a marker for genetic manipulations in transgenic mice. Nucleic Acids Res 1995; 23:4551-6; PMID:8524641; http://dx.doi.org/10.1093/nar/23.22.4551
  • Overbeek PA, Aguilar-Cordova E, Hanten G, Schaffner DL, Patel P, Lebovitz RM, Lieberman MW. Coinjection strategy for visual identification of transgenic mice. Transgenic Res 1991; 1:31-7; PMID:1844573; http://dx.doi.org/10.1007/BF02512994
  • Lupski JR. Genomic rearrangements and sporadic disease. Nat Genet 2007; 39:S43-7; PMID:17597781; http://dx.doi.org/10.1038/ng2084
  • Stankiewicz P, Lupski JR. Structural variation in the human genome and its role in disease. Annu Rev Med 2010; 61:437-55; PMID:20059347; http://dx.doi.org/10.1146/annurev-med-100708-204735
  • Consortium EP. An integrated encyclopedia of DNA elements in the human genome. Nature 2012; 489:57-74; PMID:22955616; http://dx.doi.org/10.1038/nature11247
  • Yue F, Cheng Y, Breschi A, Vierstra J, Wu W, Ryba T, Sandstrom R, Ma Z, Davis C, Pope BD, et al. A comparative encyclopedia of DNA elements in the mouse genome. Nature 2014; 515:355-64; PMID:25409824; http://dx.doi.org/10.1038/nature13992
  • Amiel J, Sproat-Emison E, Garcia-Barcelo M, Lantieri F, Burzynski G, Borrego S, Pelet A, Arnold S, Miao X, Griseri P, et al. Hirschsprung disease, associated syndromes and genetics: a review. J Med Genet 2008; 45:1-14; PMID:17965226; http://dx.doi.org/10.1136/jmg.2007.053959
  • Bergeron KF, Silversides DW, Pilon N. The developmental genetics of Hirschsprung's disease. Clin Genet 2013; 83:15-22; PMID:23043324; http://dx.doi.org/10.1111/cge.12032
  • Goldstein AM, Hofstra RM, Burns AJ. Building a brain in the gut: development of the enteric nervous system. Clin Genet 2013; 83:307-16; PMID:23167617; http://dx.doi.org/10.1111/cge.12054
  • Lake JI, Heuckeroth RO. Enteric nervous system development: migration, differentiation, and disease. Am J Physiol Gastrointestinal Liver Physiol 2013; 305:G1-24; http://dx.doi.org/10.1152/ajpgi.00452.2012
  • Obermayr F, Hotta R, Enomoto H, Young HM. Development and developmental disorders of the enteric nervous system. Nat Rev Gastroenterol Hepatol 2013; 10:43-57; PMID:23229326; http://dx.doi.org/10.1038/nrgastro.2012.234
  • Alves MM, Sribudiani Y, Brouwer RW, Amiel J, Antinolo G, Borrego S, Ceccherini I, Chakravarti A, Fernandez RM, Garcia-Barcelo MM, et al. Contribution of rare and common variants determine complex diseases-Hirschsprung disease as a model. Dev Biol 2013; 382:320-9; PMID:23707863; http://dx.doi.org/10.1016/j.ydbio.2013.05.019
  • Barlow A, de Graaff E, Pachnis V. Enteric nervous system progenitors are coordinately controlled by the G protein-coupled receptor EDNRB and the receptor tyrosine kinase RET. Neuron 2003; 40:905-16; PMID:14659090; http://dx.doi.org/10.1016/S0896-6273(03)00730-X
  • Bergeron KF, Cardinal T, Pilon N. A quantitative cell migration assay for murine enteric neural progenitors. J Visualized Exp 2013; 18(79):e50709
  • Fitzgerald J, Holden P, Hansen U. The expanded collagen VI family: new chains and new questions. Connective Tissue Res 2013; 54:345-50; http://dx.doi.org/10.3109/03008207.2013.822865
  • Gara SK, Grumati P, Urciuolo A, Bonaldo P, Kobbe B, Koch M, Paulsson M, Wagener R. Three novel collagen VI chains with high homology to the alpha3 chain. J Biol Chem 2008; 283:10658-70; PMID:18276594; http://dx.doi.org/10.1074/jbc.M709540200