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1 Stanley Division of Developmental
Neurovirology, Johns Hopkins University School of Medicine, Baltimore,
Maryland
2 Howard Hughes Medical Institute, Johns Hopkins
University School of Medicine, Baltimore, Maryland
3> Stanley Foundation Research Program,
Bethesda, Maryland, USA
Correspondence: Dr Robert H. Yolken, Theodore and Vada Stanley Professorship of Neurovirology, Johns Hopkins University, Stanley Division of Developmental Neurovirology, 600 N. Wolfe Street, Blalock IIII, Baltimore, MD 21287-4933, USA. Tel: +1 410 955 3271; fax: +1 410 955 3723; e-mail: yolken{at}welchlink.welch.jhu.edu
Declaration of interest This research was supported by the Theodore and Vada Stanley Foundation.
Background Bipolar disorder is a serious brain disease affecting more than a million individuals living in the USA. Epidemiological studies indicate a role for both genetic and environmental factors in the pathogenesis of this disorder.
Aim To identify RNA transcripts that are up- or down-regulated in the frontal cortex regions of individuals with bipolar disorder.
Method Serial analysis of gene expression (SAGE) and reverse transcriptase-polymerase chain reaction were used to identify RNA transcripts which are differentially expressed in the frontal cortex of brains obtained postmortem from individuals with bipolar disorder compared with other psychiatric and control conditions.
Results Levels of RNA transcripts encoding the serotonin transporter
protein and components of the NF-
B transcription factor complex are
significantly increased in individuals with bipolar disorder compared with
unaffected controls. Increased levels of expression of these RNA transcripts
were also detected in the brains of some individuals with schizophrenia and
unipolar depression.
Conclusion The SAGE technique offers promise for the characterisation of complex human brain diseases.
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