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 [J].
Alonso, Ana ;
Moreno, Maria ;
Ordonez, Patricia ;
Fernandez, Rebeca ;
Perez, Cristina ;
Diaz, Fernando ;
Navarro, Ana ;
Tolivia, Jorge ;
Gonzalez, Celestino .
ENDOCRINOLOGY, 2008, 149 (01) :57-72
[2]   The activity of hsp90α promoter is regulated by NF-κB transcription factors [J].
Ammirante, M. ;
Rosati, A. ;
Gentilella, A. ;
Festa, M. ;
Petrella, A. ;
Marzullo, L. ;
Pascale, M. ;
Belisario, M. A. ;
Leone, A. ;
Turco, M. C. .
ONCOGENE, 2008, 27 (08) :1175-1178
[3]   A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia [J].
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 .
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 [J].
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. .
JOURNAL OF MEDICAL GENETICS, 2010, 47 (05) :312-320
[5]   The Universal Protein Resource (UniProt) in 2010 [J].
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 .
NUCLEIC ACIDS RESEARCH, 2010, 38 :D142-D148
[6]   The novel cargo Alcadein induces vesicle association of kinesin-1 motor components and activates axonal transport [J].
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 .
EMBO JOURNAL, 2007, 26 (06) :1475-1486
[7]   Human SLITRK family genes: genomic organization and expression profiling in normal brain and brain tumor tissue [J].
Aruga, J ;
Yokota, N ;
Mikoshiba, K .
GENE, 2003, 315 :87-94
[8]   A Virtual Reality Test Identifies the Visuospatial Strengths of Adolescents with Dyslexia [J].
Attree, Elizabeth A. ;
Turner, Mark. J. ;
Cowell, Naina .
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) [J].
Bai, SM ;
Ghoshal, K ;
Jacob, ST .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (19) :13604-13611
[10]   Functional Skills of Individuals With Fragile X Syndrome: A Lifespan Cross-Sectional Analysis [J].
Bailey, Donald B., Jr. ;
Raspa, Melissa ;
Holiday, David ;
Bishop, Ellen ;
Olmsted, Murrey .
AJIDD-AMERICAN JOURNAL ON INTELLECTUAL AND DEVELOPMENTAL DISABILITIES, 2009, 114 (04) :289-303