Positive Symptoms of Psychosis Correlate With Expression of Ubiquitin Proteasome Genes in Peripheral Blood

被引:38
作者
Bousman, Chad A. [1 ]
Chana, Gursharan
Glatt, Stephen J. [2 ]
Chandler, Sharon D.
May, Todd [3 ]
Lohr, James [3 ]
Kremen, William S. [3 ]
Tsuang, Ming T. [3 ,4 ]
Everall, Ian P.
机构
[1] Univ Calif San Diego, Ctr Behav Genom, Dept Psychiat, La Jolla, CA 92039 USA
[2] SUNY Upstate Med Univ, Dept Psychiat & Behav Sci, Syracuse, NY USA
[3] Harvard Univ, VA San Diego Healthcare Syst, Boston, MA 02115 USA
[4] Harvard Univ, Dept Epidemiol & Psychiat, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
UBE2K; E2-25K/Hip-2; SIAH2; USP2; UBP41; ALPHA-SYNUCLEIN; DEUBIQUITINATING ENZYMES; PREFRONTAL CORTEX; SCHIZOPHRENIA; SYSTEM;
D O I
10.1002/ajmg.b.31106
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Several brain- and blood-based gene expression studies in patients with psychotic disorders (e. g., schizophrenia) have identified genes in the ubiquitin proteasome system (UPS) pathway as putative biomarkers. However, to date an examination of the UPS pathway in the broader context of symptom severity in psychosis has not been conducted. The purpose of this study was to investigate the correlation between clinical scores on the Scales for the Assessment of Positive and Negative Symptoms (SAPS-SANS) and expression of 43 highly annotated genes within the UPS pathway in blood from patients with psychosis. A sample of 19 psychotic patients diagnosed with schizophrenia (n = 13) or bipolar disorder (n = 6) were recruited. Pearson's partial correlations, adjusting for gender, ethnicity, age, education, medication, smoking, and past 6-month substance use, were performed between each of the selected UPS genes and both scales. Significant Bonferroni-adjusted positive associations were observed between SAPS scores and two ubiquitin conjugation genes (i.e., UBE2K, SIAH2), while a negative association was observed with one deubiquitination gene (i.e., USP2). No gene expression levels were significantly associated with scores on the SANS after correction for multiple testing. Our findings suggest that dysregulation of the UPS, specifically ubiquitin conjugation and deubiquitination, may point to a possible underlying biological mechanism for severity of positive but not negative symptoms. (c) 2010 Wiley-Liss, Inc.
引用
收藏
页码:1336 / 1341
页数:6
相关论文
共 32 条
[1]   Deficient hippocampal neuron expression of proteasome, ubiquitin, and mitochondrial genes in multiple schizophrenia cohorts [J].
Altar, CA ;
Jurata, LW ;
Charles, V ;
Lemire, A ;
Liu, P ;
Bukhman, Y ;
Young, TA ;
Bullard, J ;
Yokoe, H ;
Webster, MJ ;
Knable, MB ;
Brockman, JA .
BIOLOGICAL PSYCHIATRY, 2005, 58 (02) :85-96
[2]  
ANDREASEN NC, 1982, ARCH GEN PSYCHIAT, V39, P789
[3]   Preliminary Evidence of Ubiquitin Proteasome System Dysregulation in Schizophrenia and Bipolar Disorder: Convergent Pathway Analysis Findings from Two Independent Samples [J].
Bousman, Chad A. ;
Chana, Gursharan ;
Glatt, Stephen J. ;
Chandler, Sharon D. ;
Lucero, Ginger R. ;
Tatro, Erick ;
May, Todd ;
Lohr, James B. ;
Kremen, William S. ;
Tsuang, Ming T. ;
Everall, Ian P. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2010, 153B (02) :494-502
[4]   The ubiquitin proteasome system in neurodegenerative diseases: Sometimes the chicken, sometimes the egg [J].
Ciechanover, A ;
Brundin, P .
NEURON, 2003, 40 (02) :427-446
[5]  
Ciechanover A, 2000, BIOESSAYS, V22, P442, DOI 10.1002/(SICI)1521-1878(200005)22:5<442::AID-BIES6>3.0.CO
[6]  
2-Q
[7]   A POWER PRIMER [J].
COHEN, J .
PSYCHOLOGICAL BULLETIN, 1992, 112 (01) :155-159
[8]   Deubiquitinating enzymes: A new class of biological regulators [J].
D'Andrea, A ;
Pellman, D .
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1998, 33 (05) :337-352
[9]   Ubiquitin-conjugating enzyme E2-25K increases aggregate formation and cell death in polyglutamine diseases [J].
de Pril, Remko ;
Fischer, David F. ;
Roos, Raymund A. C. ;
van Leeuwen, Fred W. .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2007, 34 (01) :10-19
[10]   Polyglutamine tracts in schizophrenia:: gaining new insights [J].
Denghien, I ;
Joober, R ;
Rouleau, GA ;
Néri, C .
MOLECULAR PSYCHIATRY, 2000, 5 (03) :236-237