A theoretical molecular network for dyslexia: integrating available genetic findings

被引:89
作者
Poelmans, G. [2 ]
Buitelaar, J. K. [2 ]
Pauls, D. L. [3 ]
Franke, B. [1 ,4 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Donders Inst Brain Cognit & Behav, Dept Cognit Neurosci, NL-6500 HB Nijmegen, Netherlands
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Human Genet Res,Psychiat & Neurodev Genet Uni, Boston, MA USA
[4] Radboud Univ Nijmegen, Med Ctr, Donders Inst Brain Cognit & Behav, Dept Psychiat, NL-6500 HB Nijmegen, Netherlands
关键词
dyslexia; genetics; neurodevelopment; molecular network; bioinformatics; QUANTITATIVE-TRAIT LOCUS; END-PRODUCTS RAGE; ACTIVATED PROTEIN-KINASE; FAMILY-BASED ASSOCIATION; LONG-TERM POTENTIATION; FRAGILE-X-SYNDROME; READING-DISABILITY; SUSCEPTIBILITY LOCUS; DEVELOPMENTAL DYSLEXIA; NEURONAL MIGRATION;
D O I
10.1038/mp.2010.105
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Developmental dyslexia is a common specific childhood learning disorder with a strong heritable component. Previous studies using different genetic approaches have identified several genetic loci and candidate genes for dyslexia. In this article, we have integrated the current knowledge on 14 dyslexia candidate genes suggested by cytogenetic findings, linkage and association studies. We found that 10 of the 14 dyslexia candidate genes (ROBO1, KIAA0319, KIAA0319L, S100B, DOCK4, FMR1, DIP2A, GTF2I, DYX1C1 and DCDC2) fit into a theoretical molecular network involved in neuronal migration and neurite outgrowth. Based on this, we also propose three novel dyslexia candidate genes (SLIT2, HMGB1 and VAPA) from known linkage regions, and we discuss the possible involvement of genes emerging from the two reported genome-wide association studies for reading impairment-related phenotypes in the identified network. Molecular Psychiatry (2011) 16, 365-382; doi:10.1038/mp.2010.105; published online 19 October 2010
引用
收藏
页码:365 / 382
页数:18
相关论文
共 155 条
  • [1] Chronic estradiol treatment improves brain homeostasis during aging in female rats
    Alonso, Ana
    Moreno, Maria
    Ordonez, Patricia
    Fernandez, Rebeca
    Perez, Cristina
    Diaz, Fernando
    Navarro, Ana
    Tolivia, Jorge
    Gonzalez, Celestino
    [J]. ENDOCRINOLOGY, 2008, 149 (01) : 57 - 72
  • [2] The activity of hsp90α promoter is regulated by NF-κB transcription factors
    Ammirante, M.
    Rosati, A.
    Gentilella, A.
    Festa, M.
    Petrella, A.
    Marzullo, L.
    Pascale, M.
    Belisario, M. A.
    Leone, A.
    Turco, M. C.
    [J]. ONCOGENE, 2008, 27 (08) : 1175 - 1178
  • [3] A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia
    Anthoni, Heidi
    Zucchelli, Marco
    Matsson, Hans
    Mueller-Myhsok, Bertram
    Fransson, Ingegerd
    Schumacher, Johannes
    Massinen, Satu
    Onkamo, Paivi
    Warnke, Andreas
    Griesemann, Heide
    Hoffmann, Per
    Nopola-Hemmi, Jaana
    Lyytinen, Heikki
    Schulte-Koerne, Gerd
    Kere, Juha
    Noethen, Markus M.
    Peyrard-Janvid, Myriam
    [J]. HUMAN MOLECULAR GENETICS, 2007, 16 (06) : 667 - 677
  • [4] Partial 7q11.23 deletions further implicate GTF2I and GTF2IRD1 as the main genes responsible for the Williams-Beuren syndrome neurocognitive profile
    Antonell, A.
    Del Campo, M.
    Magano, L. F.
    Kaufmann, L.
    Martinez de la Iglesia, J.
    Gallastegui, F.
    Flores, R.
    Schweigmann, U.
    Fauth, C.
    Kotzot, D.
    Perez-Jurado, L. A.
    [J]. JOURNAL OF MEDICAL GENETICS, 2010, 47 (05) : 312 - 320
  • [5] The Universal Protein Resource (UniProt) in 2010
    Apweiler, Rolf
    Martin, Maria Jesus
    O'Donovan, Claire
    Magrane, Michele
    Alam-Faruque, Yasmin
    Antunes, Ricardo
    Barrell, Daniel
    Bely, Benoit
    Bingley, Mark
    Binns, David
    Bower, Lawrence
    Browne, Paul
    Chan, Wei Mun
    Dimmer, Emily
    Eberhardt, Ruth
    Fedotov, Alexander
    Foulger, Rebecca
    Garavelli, John
    Huntley, Rachael
    Jacobsen, Julius
    Kleen, Michael
    Laiho, Kati
    Leinonen, Rasko
    Legge, Duncan
    Lin, Quan
    Liu, Wudong
    Luo, Jie
    Orchard, Sandra
    Patient, Samuel
    Poggioli, Diego
    Pruess, Manuela
    Corbett, Matt
    di Martino, Giuseppe
    Donnelly, Mike
    van Rensburg, Pieter
    Bairoch, Amos
    Bougueleret, Lydie
    Xenarios, Ioannis
    Altairac, Severine
    Auchincloss, Andrea
    Argoud-Puy, Ghislaine
    Axelsen, Kristian
    Baratin, Delphine
    Blatter, Marie-Claude
    Boeckmann, Brigitte
    Bolleman, Jerven
    Bollondi, Laurent
    Boutet, Emmanuel
    Quintaje, Silvia Braconi
    Breuza, Lionel
    [J]. NUCLEIC ACIDS RESEARCH, 2010, 38 : D142 - D148
  • [6] The novel cargo Alcadein induces vesicle association of kinesin-1 motor components and activates axonal transport
    Araki, Yoichi
    Kawano, Takanori
    Taru, Hidenori
    Saito, Yuhki
    Wada, Sachiyo
    Miyamoto, Kanako
    Kobayashi, Hisako
    Ishikawa, Hiroyuki O.
    Ohsugi, Yu
    Yamamoto, Tohru
    Matsuno, Kenji
    Kinjo, Masataka
    Suzuki, Toshiharu
    [J]. EMBO JOURNAL, 2007, 26 (06) : 1475 - 1486
  • [7] Human SLITRK family genes: genomic organization and expression profiling in normal brain and brain tumor tissue
    Aruga, J
    Yokota, N
    Mikoshiba, K
    [J]. GENE, 2003, 315 : 87 - 94
  • [8] A Virtual Reality Test Identifies the Visuospatial Strengths of Adolescents with Dyslexia
    Attree, Elizabeth A.
    Turner, Mark. J.
    Cowell, Naina
    [J]. CYBERPSYCHOLOGY & BEHAVIOR, 2009, 12 (02): : 163 - 168
  • [9] RETRACTED: Identification of T-cadherin as a novel target of DNA methyltransferase 3B and its role in the suppression of nerve growth factor-mediated neurite outgrowth in PC12 cells (Retracted article. See vol. 293, pg. 3592, 2018)
    Bai, SM
    Ghoshal, K
    Jacob, ST
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (19) : 13604 - 13611
  • [10] Functional Skills of Individuals With Fragile X Syndrome: A Lifespan Cross-Sectional Analysis
    Bailey, Donald B., Jr.
    Raspa, Melissa
    Holiday, David
    Bishop, Ellen
    Olmsted, Murrey
    [J]. AJIDD-AMERICAN JOURNAL ON INTELLECTUAL AND DEVELOPMENTAL DISABILITIES, 2009, 114 (04): : 289 - 303