Genetic association of the EGR2 gene with bipolar disorder in Korea

被引:11
作者
Kim, Se Hyun [1 ]
Song, Joo Youn [2 ,3 ,4 ]
Joo, Eun Jeong [5 ]
Lee, Kyu Young [5 ]
Shin, Soon Young [6 ]
Lee, Young Han [6 ]
Ahn, Yong Min [1 ,3 ,4 ]
Kim, Yong Sik [1 ,2 ,3 ,4 ]
机构
[1] Seoul Natl Univ, Coll Med, Seoul Natl Univ Hosp, Dept Neuropsychiat, Seoul 110744, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Biomed Sci, Seoul 110744, South Korea
[3] Seoul Natl Univ, Coll Med, Dept Psychiat & Behav Sci, Seoul 110744, South Korea
[4] Seoul Natl Univ, Coll Med, Inst Human Behav Med, Seoul 110744, South Korea
[5] Eulji Univ, Sch Med, Eulji Gen Hosp, Dept Neuropsychiat, Seoul 139711, South Korea
[6] Konkuk Univ, IBST, Dept Biomed Sci & Technol, Seoul 143701, South Korea
关键词
bipolar disorder; EGR2; protein; human; genes; immediate early; genetic association studies; schizophrenia; IMMEDIATE-EARLY GENE; GENOME-WIDE ASSOCIATION; TRANSCRIPTION FACTORS; SUSCEPTIBILITY GENE; I DISORDER; EXPRESSION; SCHIZOPHRENIA; FAMILY; NEUREGULIN-1; INDUCTION;
D O I
10.3858/emm.2012.44.2.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The early growth response gene 2 (EGR2) is located at chromosome 10q21, one of the susceptibility loci in bipolar disorder (BD). EGR2 is involved in cognitive function, myelination, and signal transduction related to neuregulin-ErbB receptor, Bcl-2 family proteins, and brain-derived neurotrophic factor. This study investigated the genetic association of the EGR2 gene with BD and schizophrenia (SPR) in Korea. In 946 subjects (350 healthy controls, 352 patients with BD, and 244 with SPR), nine single nucleotide polymorphisms (SNPs) in the EGR2 gene region were genotyped. Five SNPs showed nominally significant allelic associations with BD (rs2295814, rs61865882, rs10995315, rs2297488, and rs2297489), and the positive associations of all except rs2297488 remained significant after multiple testing correction. Linkage disequilibrium structure analysis revealed two haplotype blocks. Among the common identified haplotypes (frequency > 5%), 'T-G-A-C-T (block 1)' and 'A-A-G-C (block 2)' haplotypes were over-represented, while 'C-G-G-T-T (block 1)' haplotype was under-represented in BD. In contrast, no significant associations were found with SPR. Although an extended analysis with a larger sample size or independent replication is required, these findings suggest a genetic association of EGR2 with BD. Combined with a plausible biological function of EGR2, the EGR2 gene is a possible susceptibility gene in BD.
引用
收藏
页码:121 / 129
页数:9
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