Please use this identifier to cite or link to this item: https://une.intersearch.com.au/unejspui/handle/1959.11/3206
Title: Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo
Contributor(s): Sullivan, PF (author); de Geus, EJC (author); Coventry, William L (author); Domschke, K (author); Farmer, A (author); Fava, M (author); Gordon, SD (author); He, Q (author); Heath, AC (author); Heutink, P (author); Holsboer, F (author); Hoogendijk, WJ (author); Willemsen, G (author); Hottenga, JJ (author); Hu, Y (author); Kohli, Y (author); Lin, D (author); Lucae, S (author); MacIntyre, DJ (author); Maier, W (author); McGhee, KA (author); McGuffin, P (author); Montgomery, GW (author); James, MR (author); Muir, WJ (author); Nolen, WA (author); Nothen, MM (author); Perlis, RH (author); Pirlo, K (author); Posthuma, D (author); Rietschel, M (author); Rizzu, P (author); Schosser, A (author); Smit, AB (author); Smit, JH (author); Smoller, JW (author); Tzeng, J-Y (author); van Dyck, R (author); Verhage, M (author); Zitman, FG (author); Martin, NG (author); Wray, NR (author); Boomsma, DI (author); Penninx, BWJH (author); Zandbelt, T (author); Arolt, V (author); Baune, BT (author); Blackwood, D (author); Cichon, S (author)
Publication Date: 2009
DOI: 10.1038/mp.2008.125
Handle Link: https://hdl.handle.net/1959.11/3206
Abstract: Major depressive disorder (MDD) is a common complex trait with enormous public health significance. As part of the Genetic Association Information Network initiative of the US Foundation for the National Institutes of Health, we conducted a genome-wide association study of 435 291 single nucleotide polymorphisms (SNPs) genotyped in 1738 MDD cases and 1802 controls selected to be at low liability for MDD. Of the top 200, 11 signals localized to a 167 kb region overlapping the gene piccolo (PCLO, whose protein product localizes to the cytomatrix of the presynaptic active zone and is important in monoaminergic neurotransmission in the brain) with P-values of 7.7×10⁻⁷ for rs2715148 and 1.2×10⁻⁶ for rs2522833. We undertook replication of SNPs in this region in five independent samples (6079 MDD independent cases and 5893 controls) but no SNP exceeded the replication significance threshold when all replication samples were analyzed together. However, there was heterogeneity in the replication samples, and secondary analysis of the original sample with the sample of greatest similarity yielded P=6.4×10⁻⁸ for the nonsynonymous SNP rs2522833 that gives rise to a serine to alanine substitution near a C2 calcium-binding domain of the PCLO protein. With the integrated replication effort, we present a specific hypothesis for further studies.
Publication Type: Journal Article
Source of Publication: Molecular Psychiatry, 14(4), p. 359-375
Publisher: Nature Publishing Group
Place of Publication: Houndmills, United Kingdom
ISSN: 1359-4184
Field of Research (FOR): 060405 Gene Expression (incl Microarray and other genome-wide approaches)
Peer Reviewed: Yes
HERDC Category Description: C1 Refereed Article in a Scholarly Journal
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