TY - JOUR
T1 - Genomic convergence analysis of schizoprenia
T2 - mRNA sequencing reveals altered synaptic vesicular transport in post-mortem cerebellum
AU - Mudge, Joann
AU - Miller, Neil A.
AU - Khrebtukova, Irina
AU - Lindquist, Ingrid E.
AU - May, Gregory D.
AU - Huntley, Jim J.
AU - Luo, Shujun
AU - Zhang, Lu
AU - van Velkinburgh, Jennifer C.
AU - Farmer, Andrew D.
AU - Lewis, Sharon
AU - Beavis, William D.
AU - Schilkey, Faye D.
AU - Virk, Selene M.
AU - Black, C. Forrest
AU - Myers, M. Kathy
AU - Mader, Lar C.
AU - Langley, Ray J.
AU - Utsey, John P.
AU - Kim, Ryan W.
AU - Roberts, Rosalinda C.
AU - Khalsa, Sat Kirpal
AU - Garcia, Meredith
AU - Ambriz-Griffith, Victoria
AU - Harlan, Richard
AU - Czika, Wendy
AU - Martin, Stanton
AU - Wolfinger, Russell D.
AU - Perrone-Bizzozero, Nora I.
AU - Schroth, Gary P.
AU - Kingsmore, Stephen F.
PY - 2008/11/5
Y1 - 2008/11/5
N2 - Schizophrenia (SCZ) is a common, disabling mental illness with high heritability but complex, poorly understood genetic etiology. As the first phase of a genomic convergence analysis of SCZ, we generated 16.7 billion nucleotides of short read, shotgun sequences of cDNA from post-mortem cerebellar cortices of 14 patients and six, matched controls. A rigorous analysis pipeline was developed for analysis of digital gene expression studies. Sequences aligned to approximately 33,200 transcripts in each sample, with average coverage of 450 reads per gene. Following adjustments for confounding clinical, sample and experimental sources of variation, 215 genes differed significantly in expression between cases and controls. Golgi apparatus, vesicular transport, membrane association, Zinc binding and regulation of transcription were over-represented among differentially expressed genes. Twenty three genes with altered expression and involvement in presynaptic vesicular transport, Golgi function and GABAergic neurotransmission define a unifying molecular hypothesis for dysfunction in cerebellar cortex in SCZ.
AB - Schizophrenia (SCZ) is a common, disabling mental illness with high heritability but complex, poorly understood genetic etiology. As the first phase of a genomic convergence analysis of SCZ, we generated 16.7 billion nucleotides of short read, shotgun sequences of cDNA from post-mortem cerebellar cortices of 14 patients and six, matched controls. A rigorous analysis pipeline was developed for analysis of digital gene expression studies. Sequences aligned to approximately 33,200 transcripts in each sample, with average coverage of 450 reads per gene. Following adjustments for confounding clinical, sample and experimental sources of variation, 215 genes differed significantly in expression between cases and controls. Golgi apparatus, vesicular transport, membrane association, Zinc binding and regulation of transcription were over-represented among differentially expressed genes. Twenty three genes with altered expression and involvement in presynaptic vesicular transport, Golgi function and GABAergic neurotransmission define a unifying molecular hypothesis for dysfunction in cerebellar cortex in SCZ.
UR - http://www.scopus.com/inward/record.url?scp=56649102089&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0003625
DO - 10.1371/journal.pone.0003625
M3 - Article
C2 - 18985160
AN - SCOPUS:56649102089
SN - 1932-6203
VL - 3
JO - PLoS ONE
JF - PLoS ONE
IS - 11
M1 - e3625
ER -