Gene and expression analyses reveal enhanced expression of pericentrin 2 (PCNT2) in bipolar disorder

被引:27
作者
Anitha, Ayyappan [1 ]
Nakamura, Kazuhiko [1 ]
Yamada, Kazuo
Iwayama, Yoshimi
Toyota, Tomoko
Takei, Nori [1 ]
Iwata, Yasuhide [1 ]
Suzuki, Katsuaki [1 ]
Sekine, Yoshimoto [1 ]
Matsuzaki, Hideo [3 ]
Kawai, Masayoshi [1 ]
Miyoshi, Ko [6 ]
Katayama, Taiichi [2 ]
Matsuzaki, Shinsuke [3 ,4 ]
Baba, Kousuke [7 ]
Honda, Akiko [5 ]
Hattori, Tsuyoshi [4 ]
Shimizu, Shoko [4 ]
Kumamoto, Natsuko [4 ]
Tohyama, Masaya [3 ,4 ]
Yoshikawa, Takeo
Mori, Norio [1 ]
机构
[1] Hamamatsu Univ Sch Med, Dept Psychiat & Neurol, Hamamatsu, Shizuoka 4313192, Japan
[2] Hamamatsu Univ Sch Med, Dept Anat & Neurosci, Hamamatsu, Shizuoka 4313192, Japan
[3] Ctr Child Mental Dev, Osaka Hamamatsu Joint Res, Osaka, Japan
[4] Osaka Univ, Dept Anat & Neurosci, Grad Sch Med, Suita, Osaka 565, Japan
[5] Tanabe Seiyaku Co Ltd, Pharmacol Res Lab, Osaka, Japan
[6] Okayama Univ, Dept Brain Sci, Goldman Sch Med & Dent, Okayama, Japan
[7] Kobe Univ, Sch Med, Dept Anat & Dev Neurobiol, Kobe, Hyogo 650, Japan
关键词
association study; bipolar disorder; DISC1; PCNT2; peripheral blood lymphocytes; postmortem prefrontal cortex;
D O I
10.1016/j.biopsych.2007.07.010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: DISC1 has been suggested as a causative gene for psychoses in a large Scottish kindred. PCNT2 has recently been identified as an interacting partner of DISC1. In this study, we investigated the role of PCNT2 in bipolar disorder, by gene expression analysis and genetic association study. Methods: By TaqMan real-time quantitative reverse transcriptase polymerase chain reaction (qRT-PCR), we examined the messenger RNA (mRNA) levels of PCNT2 in the postmortem prefrontal cortex of bipolar disorder (n = 34), schizophrenia (n = 31), and control subjects (n = 32), obtained from Stanley Array Collection. We also compared the mRNA levels of PCNT2 in the peripheral blood lymphocytes of bipolar disorder (n = 21), schizophrenia (n = 21), depression (n = 33), and control subjects (n = 57). For the association study, 23 single nucleotide polymorphisms (SNPs) were analyzed in 285 bipolar disorder patients and 287 age-and gender-matched control subjects, all of Japanese origin. The genotypes were determined by TaqMan assay. Results: Significantly higher expression of PCNT2 was observed in the brain samples of bipolar group, compared with the control (P = .001) and schizophrenia (p = .018) groups. In the peripheral blood lymphocytes also, a significantly higher expression of PCNT2 was observed in the bipolar group, compared with the control subjects (p = .043). However, none of the SNPs analyzed in our study showed a significant association with bipolar disorder; a weak tendency toward association was observed for two intronic SNPs. Conclusions: Our findings suggest that elevated levels of PCNT2 might be implicated in the pathophysiology of bipolar disorder.
引用
收藏
页码:678 / 685
页数:8
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