Neuropsychiatric disorders such as depression and psychosis affect 1/4 of all individuals during their lifetime, and despite efforts to improve the selectivity of psychoactive drugs, all are associated with side effects. Using a genome-wide chemogenomic assay, the authors found that these medications perturbed many evolutionarily conserved genes and cellular pathways (see Ericson et al., doi:10.1371/journal.pgen.1000151).
Image Credit: Trine Giaever
Interview
Sweating the Details: An Interview with Jamie Thomson
PLOS Genetics: published August 29, 2008 | https://doi.org/10.1371/journal.pgen.1000182
Perspectives
Rise of the Machines
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FHY1 Mediates Nuclear Import of the Light-Activated Phytochrome A Photoreceptor
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Patterns of Positive Selection in Six Mammalian Genomes
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Antagonism between DNA and H3K27 Methylation at the Imprinted Rasgrf1 Locus
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Unveiling Novel RecO Distant Orthologues Involved in Homologous Recombination
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Linkage Disequilibrium-Based Quality Control for Large-Scale Genetic Studies
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High-Precision, Whole-Genome Sequencing of Laboratory Strains Facilitates Genetic Studies
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Double Strand Breaks Can Initiate Gene Silencing and SIRT1-Dependent Onset of DNA Methylation in an Exogenous Promoter CpG Island
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Genic and Global Functions for Paf1C in Chromatin Modification and Gene Expression in Arabidopsis
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An Sp1/Sp3 Binding Polymorphism Confers Methylation Protection
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Deep Sequencing Analysis of Small Noncoding RNA and mRNA Targets of the Global Post-Transcriptional Regulator, Hfq
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Genome-Wide Scan on Total Serum IgE Levels Identifies FCER1A as Novel Susceptibility Locus
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