» Articles » PMID: 23147385

Two Gene Co-expression Modules Differentiate Psychotics and Controls

Overview
Journal Mol Psychiatry
Date 2012 Nov 14
PMID 23147385
Citations 91
Authors
Affiliations
Soon will be listed here.
Abstract

Schizophrenia (SCZ) and bipolar disorder (BD) are highly heritable psychiatric disorders. Associated genetic and gene expression changes have been identified, but many have not been replicated and have unknown functions. We identified groups of genes whose expressions varied together, that is co-expression modules, then tested them for association with SCZ. Using weighted gene co-expression network analysis, we show that two modules were differentially expressed in patients versus controls. One, upregulated in cerebral cortex, was enriched with neuron differentiation and neuron development genes, as well as disease genome-wide association study genetic signals; the second, altered in cerebral cortex and cerebellum, was enriched with genes involved in neuron protection functions. The findings were preserved in five expression data sets, including sets from three brain regions, from a different microarray platform, and from BD patients. From those observations, we propose neuron differentiation and development pathways may be involved in etiologies of both SCZ and BD, and neuron protection function participates in pathological process of the diseases.

Citing Articles

Altered Expression of PDE4 Genes in Schizophrenia: Insights from a Brain and Blood Sample Meta-Analysis and iPSC-Derived Neurons.

Burrack N, Yitzhaky A, Mizrahi L, Wang M, Stern S, Hertzberg L Genes (Basel). 2024; 15(5).

PMID: 38790238 PMC: 11121586. DOI: 10.3390/genes15050609.


Single-cell genomics and regulatory networks for 388 human brains.

Emani P, Liu J, Clarke D, Jensen M, Warrell J, Gupta C Science. 2024; 384(6698):eadi5199.

PMID: 38781369 PMC: 11365579. DOI: 10.1126/science.adi5199.


Single-cell genomics and regulatory networks for 388 human brains.

Emani P, Liu J, Clarke D, Jensen M, Warrell J, Gupta C bioRxiv. 2024; .

PMID: 38562822 PMC: 10983939. DOI: 10.1101/2024.03.18.585576.


Coexpression network analysis of the adult brain sheds light on the pathogenic mechanism of DDR1 in schizophrenia and bipolar disorder.

Aranda S, Muntane G, Vilella E Transl Psychiatry. 2024; 14(1):112.

PMID: 38395959 PMC: 10891045. DOI: 10.1038/s41398-024-02823-0.


Brain and blood transcriptome profiles delineate common genetic pathways across suicidal ideation and suicide.

Sun S, Liu Q, Wang Z, Huang Y, Sublette M, Dwork A Mol Psychiatry. 2024; 29(5):1417-1426.

PMID: 38278992 PMC: 11189724. DOI: 10.1038/s41380-024-02420-z.


References
1.
Hattori E, Liu C, Badner J, Bonner T, Christian S, Maheshwari M . Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series. Am J Hum Genet. 2003; 72(5):1131-40. PMC: 1180266. DOI: 10.1086/374822. View

2.
Jia P, Tian J, Zhao Z . Assessing gene length biases in gene set analysis of Genome-Wide Association Studies. Int J Comput Biol Drug Des. 2011; 3(4):297-310. DOI: 10.1504/IJCBDD.2010.038394. View

3.
Li Y, Willer C, Ding J, Scheet P, Abecasis G . MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes. Genet Epidemiol. 2010; 34(8):816-34. PMC: 3175618. DOI: 10.1002/gepi.20533. View

4.
Cai C, Langfelder P, Fuller T, Oldham M, Luo R, van den Berg L . Is human blood a good surrogate for brain tissue in transcriptional studies?. BMC Genomics. 2010; 11:589. PMC: 3091510. DOI: 10.1186/1471-2164-11-589. View

5.
Alexson T, Hitoshi S, Coles B, Bernstein A, van der Kooy D . Notch signaling is required to maintain all neural stem cell populations--irrespective of spatial or temporal niche. Dev Neurosci. 2006; 28(1-2):34-48. DOI: 10.1159/000090751. View