AKAPs integrate genetic findings for autism spectrum disorders

被引:57
作者
Poelmans, G. [1 ,2 ]
Franke, B. [2 ,3 ]
Pauls, D. L. [4 ]
Glennon, J. C. [1 ]
Buitelaar, J. K. [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Cognit Neurosci, Donders Inst Brain Cognit & Behav, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Psychiat, Donders Inst Brain Cognit & Behav, NL-6500 HB Nijmegen, Netherlands
[4] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Psychiat & Neurodev Genet Unit,Ctr Human Genet Re, Boston, MA USA
来源
TRANSLATIONAL PSYCHIATRY | 2013年 / 3卷
关键词
A-kinase anchor proteins; autism spectrum disorders; genetics; genome-wide association studies; DE-NOVO MUTATIONS; PROTEIN-KINASE-A; PERVASIVE DEVELOPMENTAL DISORDERS; COPY NUMBER VARIATION; LYMPHOBLASTOID CELL-LINES; MEDIAL PREFRONTAL CORTEX; CANDIDATE GENES; CLINICAL-IMPLICATIONS; REPETITIVE BEHAVIOR; EXPRESSION PROFILES;
D O I
10.1038/tp.2013.48
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Autism spectrum disorders (ASDs) are highly heritable, and six genome-wide association studies (GWASs) of ASDs have been published to date. In this study, we have integrated the findings from these GWASs with other genetic data to identify enriched genetic networks that are associated with ASDs. We conducted bioinformatics and systematic literature analyses of 200 top-ranked ASD candidate genes from five published GWASs. The sixth GWAS was used for replication and validation of our findings. Further corroborating evidence was obtained through rare genetic variant studies, that is, exome sequencing and copy number variation (CNV) studies, and/or other genetic evidence, including candidate gene association, microRNA and gene expression, gene function and genetic animal studies. We found three signaling networks regulating steroidogenesis, neurite outgrowth and (glutamatergic) synaptic function to be enriched in the data. Most genes from the five GWASs were also implicated-independent of gene size-in ASDs by at least one other line of genomic evidence. Importantly, A-kinase anchor proteins (AKAPs) functionally integrate signaling cascades within and between these networks. The three identified protein networks provide an important contribution to increasing our understanding of the molecular basis of ASDs. In addition, our results point towards the AKAPs as promising targets for developing novel ASD treatments.
引用
收藏
页码:e270 / e270
页数:11
相关论文
共 108 条
  • [81] Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders
    Rosenfeld, Jill A.
    Ballif, Blake C.
    Torchia, Beth S.
    Sahoo, Trilochan
    Ravnan, J. Britt
    Schultz, Roger
    Lamb, Allen
    Bejjani, Bassem A.
    Shaffer, Lisa G.
    [J]. GENETICS IN MEDICINE, 2010, 12 (11) : 694 - 702
  • [82] Rossignol DA, 2009, ANN CLIN PSYCHIATRY, V21, P213
  • [83] Gene expression profiles following exposure to a developmental neurotoxicant, Aroclor 1254: Pathway analysis for possible mode(s) of action
    Royland, Joyce E.
    Kodavanti, Prasada Rao S.
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 2008, 231 (02) : 179 - 196
  • [84] Variants in Several Genomic Regions Associated with Asperger Disorder
    Salyakina, D.
    Ma, D. Q.
    Jaworski, J. M.
    Konidari, I.
    Whitehead, P. L.
    Henson, R.
    Martinez, D.
    Robinson, J. L.
    Sacharow, S.
    Wright, H. H.
    Abramson, R. K.
    Gilbert, J. R.
    Cuccaro, M. L.
    Pericak-Vance, M. A.
    [J]. AUTISM RESEARCH, 2010, 3 (06) : 303 - 310
  • [85] De novo mutations revealed by whole-exome sequencing are strongly associated with autism
    Sanders, Stephan J.
    Murtha, Michael T.
    Gupta, Abha R.
    Murdoch, John D.
    Raubeson, Melanie J.
    Willsey, A. Jeremy
    Ercan-Sencicek, A. Gulhan
    DiLullo, Nicholas M.
    Parikshak, Neelroop N.
    Stein, Jason L.
    Walker, Michael F.
    Ober, Gordon T.
    Teran, Nicole A.
    Song, Youeun
    El-Fishawy, Paul
    Murtha, Ryan C.
    Choi, Murim
    Overton, John D.
    Bjornson, Robert D.
    Carriero, Nicholas J.
    Meyer, Kyle A.
    Bilguvar, Kaya
    Mane, Shrikant M.
    Sestan, Nenad
    Lifton, Richard P.
    Guenel, Murat
    Roeder, Kathryn
    Geschwind, Daniel H.
    Devlin, Bernie
    State, Matthew W.
    [J]. NATURE, 2012, 485 (7397) : 237 - U124
  • [86] Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
    Sanders, Stephan J.
    Ercan-Sencicek, A. Gulhan
    Hus, Vanessa
    Luo, Rui
    Murtha, Michael T.
    Moreno-De-Luca, Daniel
    Chu, Su H.
    Moreau, Michael P.
    Gupta, Abha R.
    Thomson, Susanne A.
    Mason, Christopher E.
    Bilguvar, Kaya
    Celestino-Soper, Patricia B. S.
    Choi, Murim
    Crawford, Emily L.
    Davis, Lea
    Wright, Nicole R. Davis
    Dhodapkar, Rahul M.
    DiCola, Michael
    DiLullo, Nicholas M.
    Fernandez, Thomas V.
    Fielding-Singh, Vikram
    Fishman, Daniel O.
    Frahm, Stephanie
    Garagaloyan, Rouben
    Goh, Gerald S.
    Kammela, Sindhuja
    Klei, Lambertus
    Lowe, Jennifer K.
    Lund, Sabata C.
    McGrew, Anna D.
    Meyer, Kyle A.
    Moffat, William J.
    Murdoch, John D.
    O'Roak, Brian J.
    Ober, Gordon T.
    Pottenger, Rebecca S.
    Raubeson, Melanie J.
    Song, Youeun
    Wang, Qi
    Yaspan, Brian L.
    Yu, Timothy W.
    Yurkiewicz, Liana R.
    Beaudet, Arthur L.
    Cantor, Rita M.
    Curland, Martin
    Grice, Dorothy E.
    Guenel, Murat
    Lifton, Richard P.
    Mane, Shrikant M.
    [J]. NEURON, 2011, 70 (05) : 863 - 885
  • [87] Investigation of post-transcriptional gene regulatory networks associated with autism spectrum disorders by microRNA expression profiling of lymphoblastoid cell lines
    Sarachana, Tewarit
    Zhou, Rulun
    Chen, Guang
    Manji, Husseini K.
    Hu, Valerie W.
    [J]. GENOME MEDICINE, 2010, 2
  • [88] Inter-regional brain communication and its disturbance in autism
    Schipul, Sarah E.
    Keller, Timothy A.
    Just, Marcel Adam
    [J]. FRONTIERS IN SYSTEMS NEUROSCIENCE, 2011, 5
  • [89] Sex-specific serum biomarker patterns in adults with Asperger's syndrome
    Schwarz, E.
    Guest, P. C.
    Rahmoune, H.
    Wang, L.
    Levin, Y.
    Ingudomnukul, E.
    Ruta, L.
    Kent, L.
    Spain, M.
    Baron-Cohen, S.
    Bahn, S.
    [J]. MOLECULAR PSYCHIATRY, 2011, 16 (12) : 1213 - 1220
  • [90] Altered Functional Connectivity in Frontal Lobe Circuits Is Associated with Variation in the Autism Risk Gene CNTNAP2
    Scott-Van Zeeland, Ashley A.
    Abrahams, Brett S.
    Alvarez-Retuerto, Ana I.
    Sonnenblick, Lisa I.
    Rudie, Jeffrey D.
    Ghahremani, Dara
    Mumford, Jeanette A.
    Poldrack, Russell A.
    Dapretto, Mirella
    Geschwind, Daniel H.
    Bookheimer, Susan Y.
    [J]. SCIENCE TRANSLATIONAL MEDICINE, 2010, 2 (56)