Genetic Analyses of Roundabout (ROBO) Axon Guidance Receptors in Autism

被引:71
作者
Anitha, A. [1 ]
Nakamura, Kazuhiko [1 ]
Yamada, Kazuo [2 ]
Suda, Shiro [1 ]
Thanseem, Ismail [1 ]
Tsujii, Masatsugn [3 ,4 ]
Iwayama, Yoshimi [2 ]
Hattori, Eiji [2 ]
Toyota, Tomoko [2 ]
Miyachi, Taishi [4 ]
Iwata, Yasuhide [1 ]
Suzuki, Katsuaki [1 ]
Matsuzaki, Hideo [5 ]
Kawai, Masayoshi [1 ]
Sekine, Yoshimoto [1 ]
Tsuchiya, Kenji [1 ]
Sugihara, Gen-ichi [4 ]
Ouchi, Yasuomi [4 ,6 ]
Sugiyama, Toshiro [7 ]
Koizumi, Keita [8 ]
Higashida, Haruhiro [9 ]
Takei, Nori [1 ]
Yoshikawa, Takeo [2 ]
Mori, Norio [1 ,4 ]
机构
[1] Hamamatsu Univ Sch Med, Dept Psychiat & Neurol, Hamamatsu, Shizuoka 4313192, Japan
[2] RIKEN, Brain Sci Inst, Lab Mol Psychiat, Saitama, Japan
[3] Chukyo Univ, Fac Sociol, Aichi, Japan
[4] Hamamatsu Univ Sch Med, Osaka Hamamatsu Joint Res Ctr Child Mental Dev, Hamamatsu, Shizuoka 4313192, Japan
[5] Osaka Univ, Grad Sch Med, Osaka Hamamatsu Joint Res Ctr Child Mental Dev, Osaka, Japan
[6] Hamamatsu Med Ctr, Positron Med Ctr, Hamamatsu, Shizuoka, Japan
[7] Aichi Childrens Hlth & Med Ctr, Aichi, Japan
[8] Kanazawa Univ, Adv Sci Res Ctr, Kanazawa, Ishikawa, Japan
[9] Kanazawa Univ, Grad Sch Med, Dept Biophys Genet, Kanazawa, Ishikawa, Japan
关键词
autism; ROBO; axon; serotonin; lymphocyte expression;
D O I
10.1002/ajmg.b.30697
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Autism is a pervasive developmental disorder diagnosed in early childhood. Abnormalities of serotonergic neurotransmission have been reported in autism. Serotonin transporter (SERT) modulates serotonin levels, and is a major therapeutic target in autism. Factors that regulate SERT expression might be implicated in the pathophysiology of autism. One candidate SERT regulatory protein is the roundabout axon guidance molecule, ROBO. SerT expression in Drosophila is regulated by robo; it plays a vital role in mammalian neurodevelopment also. Here, we examined the associations of ROBO3 and ROBO4 with autism, in a trio association study using DNA from 252 families recruited to AGRE. Four SNPs of ROBO3 (rs3923890, P = 0.023; rs7925879, P = 0.017; rs4606490, P = 0.033; and rs3802905, P = 0.049) and a single SNP of ROBO4 (rs6590109, P = 0.009) showed associations with autism; the A/A genotype of rs3923890 showed lower ADI-R_A scores, which reflect social interaction. Significant haplotype associations were also observed for ROBO3 and ROBO4. We further compared the mRNA expressions of ROBO1, ROBO2, ROBO3, and ROBO4 in the lymphocytes of 19 drug-naive autistic patients and 20 age- and sex-matched controls. Expressions of ROBO1 (P = 0.018) and ROBO2 (P = 0.023) were significantly reduced in the autistic group; the possibility of using the altered expressions of ROBO as peripheral markers for autism, may be explored. In conclusion, we suggest a possible role of ROBO in the pathogenesis of autism. Abnormalities of ROBO may lead to autism either by interfering with serotonergic system, or by disrupting neurodevelopment. To the best of our knowledge, this is the first report relating ROBO with autism. (C) 2008 Wiley-Liss, Inc.
引用
收藏
页码:1019 / 1027
页数:9
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