DYX1C1 functions in neuronal migration in developing neocortex

Neuroscience

Volumn 143, Issue 2, 2006, Pages 515-522

  Wang, Y ^a   Paramasivam, M ^a   Thomas, A ^a   Bai, J ^a   Kaminen Ahola, N ^b   Kere, J ^b,c   Voskuil, J ^d   Rosen, G D ^e   Galaburda, A M ^e   Loturco, J J ^a  

^a UNIVERSITY OF CONNECTICUT   (United States)

^b UNIVERSITY OF HELSINKI   (Finland)

^c KAROLINSKA INSTITUTE   (Sweden)

^d Everest Biotech Ltd   (United Kingdom)

^e BETH ISRAEL DEACONESS MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PROTEIN DYX1C1; RNA; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; BRAIN CORTEX; CARBOXY TERMINAL SEQUENCE; CELL MIGRATION; CELL NUCLEUS; CELLULAR DISTRIBUTION; CONTROLLED STUDY; CYTOPLASM; EMBRYO; EXPERIMENTATION; FEMALE; GENE FUNCTION; GENE OVEREXPRESSION; GENETIC TRANSFECTION; NEOCORTEX; NERVE CELL; NONHUMAN; PRIORITY JOURNAL; RAT; RNA INTERFERENCE; UTERUS;

ANALYSIS OF VARIANCE; ANIMALS; BLOTTING, WESTERN; BROMODEOXYURIDINE; CELL MOVEMENT; CERCOPITHECUS AETHIOPS; COS CELLS; ELECTROPORATION; EMBRYO; GENE EXPRESSION REGULATION, DEVELOPMENTAL; MUTAGENESIS; NEOCORTEX; NEURONS; NUCLEAR PROTEINS; ORGANOGENESIS; PROTEIN STRUCTURE, TERTIARY; RATS; RNA, SMALL INTERFERING; TRANSFECTION;

EID: 33751251057     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroscience.2006.08.022     Document Type: Article

References (29)

1. Bai J., Ramos R.L., Ackman J.B., Thomas A.M., Lee R.V., and Loturco J.J. RNAi reveals doublecortin is required for radial migration in rat neocortex. Nat Neurosci 6 (2003) 1277-1283
2. Boehm G.W., Sherman G.F., Rosen G.D., Galaburda A.M., and Denenberg V.H. Neocortical ectopias in BXSB mice: effects upon reference and working memory systems. Cereb Cortex 6 (1996) 696-700
3. Chang B.S., Ly J., Appignani B., Bodell A., Apse K.A., Ravenscroft R.S., Sheen V.L., Doherty M.J., Hackney D.B., O'Connor M., Galaburda A.M., and Walsh C.A. Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia. Neurology 64 (2005) 799-803
4. Fitch R.H., Tallal P., Brown C.P., Galaburda A.M., and Rosen G.D. Induced microgyria and auditory temporal processing in rats: a model for language impairment?. Cereb Cortex 4 (1994) 260-270
5. Galaburda A.M., Sherman G.F., Rosen G.D., Aboitiz F., and Geschwind N. Developmental dyslexia: four consecutive patients with cortical anomalies. Ann Neurol 18 (1985) 222-233
6. Hannula-Jouppi K., Kaminen-Ahola N., Taipale M., Eklund R., Nopola-Hemmi J., Kaariainen H., and Kere J. The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia. PLoS Genet 1 (2005) e50
7. Hatakeyama S., Matsumoto M., Yada M., and Nakayama K.I. Interaction of U-box-type ubiquitin-protein ligases (E3s) with molecular chaperones. Genes Cells 9 (2004) 533-548
8. Kidd T., Brose K., Mitchell K.J., Fetter R.D., Tessier-Lavigne M., Goodman C.S., and Tear G. Roundabout controls axon crossing of the CNS midline and defines a novel subfamily of evolutionarily conserved guidance receptors. Cell 92 (1998) 205-215
9. Kriegstein A.R., and Noctor S.C. Patterns of neuronal migration in the embryonic cortex. Trends Neurosci 27 (2004) 392-399
10. Long H., Sabatier C., Ma L., Plump A., Yuan W., Ornitz D.M., Tamada A., Murakami F., Goodman C.S., and Tessier-Lavigne M. Conserved roles for Slit and Robo proteins in midline commissural axon guidance. Neuron 42 (2004) 213-223
11. Loturco J.J., and Bai J. The multipolar stage and disruptions in neuronal migration. Trends Neurosci 29 (2006) 407-413
12. Marino C., Giorda R., Luisa Lorusso M., Vanzin L., Salandi N., Nobile M., Citterio A., Beri S., Crespi V., Battaglia M., and Molteni M. A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia. Eur J Hum Genet 13 (2005) 491-499
13. Meng H., Hager K., Held M., Page G.P., Olson R.K., Pennington B.F., Defries J.C., Smith S.D., and Gruen J.R. TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort. Hum Genet 118 (2005) 1-4
14. Nagano T., Morikubo S., and Sato M. Filamin A and FILIP (filamin A-interacting protein) regulate cell polarity and motility in neocortical subventricular and intermediate zones during radial migration. J Neurosci 24 (2004) 9648-9657
15. Noctor S.C., Flint A.C., Weissman T.A., Wong W.S., Clinton B.K., and Kriegstein A.R. Dividing precursor cells of the embryonic cortical ventricular zone have morphological and molecular characteristics of radial glia. J Neurosci 22 (2002) 3161-3173
16. Okada A., Lansford R., Weimann J.M., Fraser S.E., and McConnell S.K. Imaging cells in the developing nervous system with retrovirus expressing modified green fluorescent protein. Exp Neurol 156 (1999) 394-406
17. Paracchini S., Thomas A., Castro S., Lai C., Paramasivam M., Wang Y., Keating B.J., Taylor J.M., Hacking D.F., Scerri T., Francks C., Richardson A.J., Wade-Martins R., Stein J.F., Knight J.C., Copp A.J., Loturco J., and Monaco A.P. The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Hum Mol Genet 15 (2006) 1659-1666
18. Peiffer A.M., Friedman J.T., Rosen G.D., and Fitch R.H. Impaired gap detection in juvenile microgyric rats. Brain Res Dev Brain Res 152 (2004) 93-98
19. Peiffer A.M., McClure M.M., Threlkeld S.W., Rosen G.D., and Fitch R.H. Severity of focal microgyria and associated rapid auditory processing deficits. Neuroreport 15 (2004) 1923-1926
20. Pennington B.F., and Smith S.D. Genetic influences on learning disabilities and speech and language disorders. Child Dev 54 (1983) 369-387
21. Scerri T.S., Fisher S.E., Francks C., MacPhie I.L., Paracchini S., Richardson A.J., Stein J.F., and Monaco A.P. Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK. J Med Genet 41 (2004) 853-857
22. Smith S.D., Kelley P.M., and Brower A.M. Molecular approaches to the genetic analysis of specific reading disability. Hum Biol 70 (1998) 239-256
23. Sokol D.K., Golomb M.R., Carvahlo K.S., and Edwards-Brown M. Reading impairment in the neuronal migration disorder of periventricular nodular heterotopia. Neurology 66 (2006) 294 author reply 294
24. Steensgaard P., Garre M., Muradore I., Transidico P., Nigg E.A., Kitagawa K., Earnshaw W.C., Faretta M., and Musacchio A. Sgt1 is required for human kinetochore assembly. EMBO Rep 5 (2004) 626-631
25. Tabata H., and Nakajima K. Multipolar migration: the third mode of radial neuronal migration in the developing cerebral cortex. J Neurosci 23 (2003) 9996-10001
26. Taipale M., Kaminen N., Nopola-Hemmi J., Haltia T., Myllyluoma B., Lyytinen H., Muller K., Kaaranen M., Lindsberg P.J., Hannula-Jouppi K., and Kere J. A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain. Proc Natl Acad Sci U S A 100 (2003) 11553-11558
27. Tsai J.W., Chen Y., Kriegstein A.R., and Vallee R.B. LIS1 RNA interference blocks neural stem cell division, morphogenesis, and motility at multiple stages. J Cell Biol 170 (2005) 935-945
28. Wong K., Ren X.R., Huang Y.Z., Xie Y., Liu G., Saito H., Tang H., Wen L., Brady-Kalnay S.M., Mei L., Wu J.Y., Xiong W.C., and Rao Y. Signal transduction in neuronal migration: roles of GTPase activating proteins and the small GTPase Cdc42 in the Slit-Robo pathway. Cell 107 (2001) 209-221
29. Yu J.Y., DeRuiter S.L., and Turner D.L. RNA interference by expression of short-interfering RNAs and hairpin RNAs in mammalian cells. Proc Natl Acad Sci U S A 99 (2002) 6047-6052