Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0036341 (
schizophrenia
)
60,220
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Genetic and molecular studies have implicated the
Bromodomain containing 1
(
BRD1
) gene in the pathogenesis of
schizophrenia
and bipolar disorder. Accordingly, mice heterozygous for a targeted deletion of Brd1 (Brd1
+/-
mice) show behavioral phenotypes with broad translational relevance to psychiatric disorders.
BRD1
encodes a scaffold protein that affects the expression of many genes through modulation of histone acetylation.
BRD1
target genes have been identified in cell lines; however the impact of reduced Brd1 levels on the brain proteome is largely unknown. In this study, we applied label-based quantitative mass spectrometry to profile the frontal cortex, hippocampus and striatum proteome and synaptosomal proteome of female Brd1
+/-
mice. We successfully quantified between 1537 and 2196 proteins and show widespread changes in protein abundancies and compartmentalization. By integrative analysis of human genetic data, we find that the differentially abundant proteins in frontal cortex and hippocampus are enriched for
schizophrenia
risk further linking the actions of
BRD1
to psychiatric disorders. Affected proteins were further enriched for proteins involved in processes known to influence neuronal and dendritic spine morphology e.g. regulation of cytoskeleton dynamics and mitochondrial function. Directly prompted in these findings, we investigated dendritic spine morphology of pyramidal neurons in anterior cingulate cortex and found them significantly altered, including reduced size of small dendritic spines and decreased number of the mature mushroom type. Collectively, our study describes known as well as new mechanisms related to
BRD1
dysfunction and its role in psychiatric disorders, and provides evidence for the molecular and cellular dysfunctions underlying altered neurosignalling and cognition in Brd1
+/-
mice.
...
PMID:Brain proteome changes in female Brd1
+/-
mice unmask dendritic spine pathology and show enrichment for schizophrenia risk. 3059 Jan 79