Behavioral Phenotypic Properties of a Natural Occurring Rat Model of Congenital Stationary Night Blindness With Cacna1f Mutation

References

• Bayley, P. R., & Morgans, C. W. (2007).Rod bipolar cells and horizontal cells form displaced synaptic contacts with rods in the outer nuclear layer of the nob2 retina.J Comp Neurol, 500, 286–298.
   PubMedGoogle Scholar
• Bech-Hansen, N. T., Naylor, M. J., Maybaum, T. A., Sparkes, R. L., Koop, B., Birch, D. G., Bergen, A. A., Prinsen, C. F., Polomeno, R. C., Gal, A., Drack, A. V., Musarella, M. A., Jacobson, S. G., Young, R. S. , & Weleber, R. G. (2000).Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-1inked complete congenital stationary night blindness.Nat Genet, 26, 319–323.
   PubMed Web of Science ®Google Scholar
• Bellone, R. R., Forsyth, G., Leeb, T., Archer, S., Sigurdsson, S., Imsland, F., Mauceli, E., Engensteiner, M., Bailey, E., Sandmeyer, L., Grahn, B., Lindblad-Toh, K., & Wade, C. M. (2010).Fine-mapping and mutation analysis of TRPM1: A candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses.Brief Funct Genomics, 9, 193–207.
   PubMed Web of Science ®Google Scholar
• Blank, M., Blake, D. J., Kröger, S. (2002). Molecular diversity of the dystrophin-like protein complex in the developing and adult avian retina. Neuroscience, 111, 259–273.
   PubMed Web of Science ®Google Scholar
• Canals, J. M., Pineda, J. R., Torres-Peraza, J. F., Bosch, M., Martin-Ibanez, R., Munoz, M. T., Mengod, G., Ernfors, P., & Alberch, J. (2004).Brain-derived neurotrophic factor regulates the onset and severity of motor dysfunction associated with enkephalinergic neuronal degeneration in Huntington's disease.J Neurosci, 24, 7727–7739.
   PubMed Web of Science ®Google Scholar
• Candille, S. I., Pardue, M. T., McCall, M. A., Peachey, N. S., & Gregg, R. G. (1999).Localization of the mouse nob (no b-wave) gene to the centromeric region of the X-chromosome.Invest Ophthalmol Vis Sci, 40, 2748–2751.
   PubMed Web of Science ®Google Scholar
• Cao, F. L., Liu, M. G., Hao, J., Li, Z., Lu, Z. M., & Chen, J. (2007).Different roles of spinal p38 and c-Jun N-terminal kinase pathways in bee venom-induced multiple pain-related behaviors.Neurosci Lett, 427, 50–54.
   PubMed Web of Science ®Google Scholar
• Carr, R. E. (1974).Congenital stationary nightblindness.Trans Am Ophthalmol Soc, 72, 448–487.
   PubMedGoogle Scholar
• Chang, B., Heckenlively, J. R., Bayley, P. R., Brecha, N. C., Davisson, M. T., Hawes, N. L., Hirano, A. A., Hurd, R. E., Ikeda, A., Johnson, B. A., McCall, M. A., Morgans, C. W., Nusinowitz, S., Peachey, N. S., Rice, D. S., Vessey, K. A., & Gregg, R. G. (2006).The nob2 mouse, a null mutation in Cacna1f: Anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses.Vis Neurosci, 23, 11–24.
   PubMed Web of Science ®Google Scholar
• Claro, F. T., Patti, C. T., Abílio, V. C., Frussa-Filho, R., & Silva, R. H. (2006).Bovine brain phosphatidylserine attenuates scopolamine induced amnesia in mice.Prog Neuropsychopharmacol Biol Psychiatry, 30, 881–886.
   PubMed Web of Science ®Google Scholar
• Drapeau, E., Mayo, W., Aurousseau, C., Le Moal, M., Piazza, P. V., & Abrous, D. N. (2003).Spatial memory performances of aged rats in the water maze predict levels of hippocampal neurogenesis.Proc Natl Acad Sci USA, 100, 14385–14390.
   PubMed Web of Science ®Google Scholar
• Francois, J., Verriest, G., & De, R. A. (1965).A new pedigree of idiopathic congenital night-blindness, transmitted as a dominant hereditary trait.Am J Ophthalmol, 59, 621–625.
   PubMed Web of Science ®Google Scholar
• Gregg, R. G., Mukhopadhyay, S., Candille, S. I., Ball, S. L., Pardue, M. T., McCall, M. A., & Peachey, N. S. (2003).Identification of the gene and the mutation responsible for the mouse nob phenotype.Invest Ophthalmol Vis Sci, 44, 378–384.
   PubMed Web of Science ®Google Scholar
• Gu, Y., Wang, L., Zhou, J., Guo, Q., Liu, N., Ding, Z., Li, L., Liu, X., An, J., Yan, G., Yao, L., & Zhang, Z. (2008).A naturally-occurring mutation in Cacna1f in a rat model of congenital stationary night blindness.Mol Vis, 14, 20–28.
   PubMed Web of Science ®Google Scholar
• Hu, D., Serrano, F., Oury, T. D., & Klann, E. (2006).Aging-dependent alterations in synaptic plasticity and memory in mice that overexpress extracellular superoxide dismutase.J Neurosci, 26, 3933–3941.
   PubMed Web of Science ®Google Scholar
• Johnson, E. L., Fetter, R. D., & Davis, G. W. (2009).Negative regulation of active zone assembly by a newly identified SR protein kinase.PLoS Biol, 7, 1–17.
   Web of Science ®Google Scholar
• Khouri, G., Mets, M. B., Smith, V. C., Wendell, M., & Pass, A. S. (1988).X-linked congenital stationary night blindness. Review and report of a family with hyperopia.Arch Ophthalmol. 106, 1417–1422.
   PubMedGoogle Scholar
• Kotturi, M. F., & Jefferies, W. A. (2005).Molecular characterization of L-type calcium channel splice variants expressed in human T lymphocytes.Mol Immunol, 42, 1461–1474.
   PubMed Web of Science ®Google Scholar
• Mansergh, F., Orton, N. C., Vessey, J. P., Lalonde, M. R., Stell, W. K., Tremblay, F., Barnes, S., Rancourt, D. E., & Bech-Hansen, N. T. (2005).Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina.Hum Mol Genet, 14, 3035–3046.
   PubMed Web of Science ®Google Scholar
• Manabe, Y., Narai, H., Warita, H., Hayashi, T., Shiro, Y., Sakai, K., Kashihara, K., Shoji, M., Abe, K. (2002). Benign adult familial myoclonic epilepsy (BAFME) with night blindness. Seizure, 11, 266–268.
   PubMed Web of Science ®Google Scholar
• McFadyen, M. P., Kusek, G., Bolivar, V. J., & Flaherty, L. (2003).Differences among eight inbred strains of mice in motor ability and motor learning on a rotorod.Genes Brain Behav, 2, 214–219.
   PubMed Web of Science ®Google Scholar
• McRory, J. E., Hamid, J., Doering, C. J., Garcia, E., Parker, R., Hamming, K., Chen, L., Hildebrand, M., Beedle, A. M., Feldcamp, L., Zamponi, G. W., & Snutch, T. P. (2004).The CACNA1F gene encodes an L-type calcium channel with unique biophysical properties and tissue distribution.J Neurosci, 24, 1707–1718.
   PubMedGoogle Scholar
• Merin, S., Rowe, H., Auerbach, E., & Landau, J. W. (1970).Syndrome of congenital high myopia with nyctalopia. Report of findings in 25 families.Am J Ophthalmol, 70, 541–547.
   PubMed Web of Science ®Google Scholar
• Miyake, Y., Yagasaki, K., Horiguchi, M., Kawase, Y., & Kanda, T. (1986).Congenital stationary night blindness with negative electroretinogram a new classification.Arch Ophthalmol, 104, 1013–1020.
   PubMedGoogle Scholar
• Pillers, D. A., Fitzgerald, K. M., Duncan, N. M., Rash, S.M., White, R.A., Dwinnell, S.J., Powell, B.R., Schnur, R.E., Ray, P.N., Cibis, G.W., Weleber, R.G. (1999). Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutations. Hum Genet, 105, 2–9.
   PubMed Web of Science ®Google Scholar
• Pillers, D. M., Bulman, D. E., Weleber, R. G., Sigesmund, D. A., Musarella, M. A., Powell, B. R., Murphey, W. H., Westall, C., Panton, C., Becker, L. E., Worton, R. G., Ray, P. N. (1993). Dystrophin expression in the human retina is required for normal function as defined by electroretinography. Nat Genet, 4, 82–86.
   PubMed Web of Science ®Google Scholar
• >Dystrophin expression in the human retina is required for normal function as defined by electroretinography. Nat Genet, 4, 82–86.
   PubMed Web of Science ®Google Scholar
• Pinto, L. H., & Enroth-Cugell, C. (2000).Tests of the mouse visual system.Mamm Genome, 11, 531–536.
   PubMed Web of Science ®Google Scholar
• Prusky, G. T., West, P. W., & Douglas, R. M. (2000).Reduced visual acuity impairs place but not cued learning in the Morris water task.Behav Brain Res, 116, 135–140.
   PubMed Web of Science ®Google Scholar
• Pusch, C. M., Zeitz, C., Brandau, O., Pesch, K., Achatz, H., Feil, S., Scharfe, C., Maurer, J., Jacobi, F. K., Pinckers, A., Andreasson, S., Hardcastle, A., Wissinger, B., Berger, W., & Meindl, A. (2000).The complete form of X-linked congenital stationary night blindness is cause by mutations in a gene encoding a leucine-rich repeat protein.Nat Genet, 26, 324–327.
   PubMed Web of Science ®Google Scholar
• Racine, J., Behn, D., Simard, E., & Lachapelle, P. (2003).Spontaneous occurrence of a potentially night blinding disorder in guinea pigs.Doc Ophthalmol, 107, 59–69.
   PubMed Web of Science ®Google Scholar
• Ripps, H. (1982).Night blindness revisited: From man to molecules.Invest Ophthalmol Vis Sci, 23, 588–609.
   PubMed Web of Science ®Google Scholar
• Robinson, L., Bridge, H., & Riedel, G. (2001).Research report: Visual discrimination learning in the water maze: A novel test for visual acuity.Behav Brain Res, 119, 77–84.
   PubMedGoogle Scholar
• Rogers, D. C., Jones, D. N. C., Nelson, P. R., Jones, C. M., Quilter, C. A., Robinson, T. L., & Hagan, J. J. (1999).Use of SHIRPA and discriminant analysis to characterise marked differences in the behavioural phenotype of six inbred mouse strains.Behav Brain Res, 105, 207–217.
   PubMed Web of Science ®Google Scholar
• Spencer, R. L., O'steen, W. K., & McEwen, B. S. (1995).Water maze performance of aged Sprague-Dawley rats in relation to retinal morphologic measures.Behav Brain Res, 68 , 139–150.
   PubMed Web of Science ®Google Scholar
• Strom, T. M., Nyakatura, G., Apfelstedt-Sylla, E., Hellebrand, H., Lorenz, B., Weber, B. H., Wutz, K., Gutwillinger, N., Rüther, K., Drescher, B., Sauer, C., Zrenner, E., Meitinger, T., Rosenthal, A., & Meindl, A. (1998).An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.Nat Genet, 19, 260–263.
   PubMed Web of Science ®Google Scholar
• Wersinger, E., Bordais, A., Schwab, Y., Sene, A., Bénard, R., Alunni, V., Sahel, J.A., Rendon, A., Roux, M.J. (2011). Reevaluation of dystrophin localization in the mouse retina. Invest Ophthalmol Vis Sci, 52, 7901–7908.
   PubMed Web of Science ®Google Scholar
• Yvert, G., Lindenberg, K. S., Picaud, S., Landwehrmeyer, G. B., Sahel, J. A., & Mandel, J. L. (2000).Expanded polyglutamines induce neurodegeneration and trans-neuronal alter ations in cerebellum and retina of SCA7 transgenic mice.Hum Mol Genet, 9, 2491–2506.
   PubMed Web of Science ®Google Scholar
• Zhang, Z., Gu, Y., Li, L., Long, T., Guo, Q., & Shi, L. (2003).A potential spontaneous rat model of X-linked congenital stationary night blindness.Doc Ophthalmol, 107, 53–57.
   PubMed Web of Science ®Google Scholar
• Zhao, J., Uchino, M., Yoshioka, K., Miyatake, M., Miike, T. (1991). Dystrophin in control and mdx retina. Brain Dev, 13, 135–137.
   PubMed Web of Science ®Google Scholar