A functional polymorphism in the succinate-semialdehyde dehydrogenase (aldehyde dehydrogenase 5 family, member A1) gene is associated with cognitive ability

被引:42
作者
Plomin, R
Turic, DM
Hill, L
Turic, DE
Stephens, M
Williams, J
Owen, MJ
O'Donovan, MC
机构
[1] Cardiff Univ, Dept Psychol Med, Cardiff CF14 4XN, S Glam, Wales
[2] Inst Psychiat, Social Genet & Dev Psychiat Ctr, London, England
基金
英国医学研究理事会;
关键词
succinate-semialdehyde dehydrogenase (SSADH); functional polymorphism; QTL; cognition; intelligence;
D O I
10.1038/sj.mp.4001441
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
Succinate-semialdehyde dehydrogenase (SSADH) deficiency is a rare cause of learning disability. We have investigated SSADH to assess its contribution to cognitive ability in the general population in both case-control- and family-based analyses. Sequence analysis of SSADH revealed four changes affecting the encoded protein, only one of which had a minor allele whose frequency is even moderately common. We genotyped this functional polymorphism in 197 high-IQ cases, 201 average-IQ controls and 196 parent high-IQ offspring trios. The minor allele was significantly less frequent in high-IQ cases and was significantly less frequently transmitted by parents to high-IQ subjects than chance expectation. A previous study has shown that the minor allele encodes a lower activity enzyme than the major allele. These data suggest that higher SSADH activity is associated with higher intelligence across the general population. The effect is small, with each allele having an effect size translating to about 1.5 IQ points.
引用
收藏
页码:582 / 586
页数:5
相关论文
共 37 条
[1]   Comparative sequencing of the proneurotensin gene and association studies in schizophrenia [J].
Austin, J ;
Hoogendoorn, B ;
Buckland, P ;
Speight, G ;
Cardno, A ;
Bowen, T ;
Williams, N ;
Spurlock, G ;
Sanders, R ;
Jones, L ;
Murphy, K ;
McCarthy, G ;
McGuffin, P ;
Owen, MJ ;
O'Donovan, MC .
MOLECULAR PSYCHIATRY, 2000, 5 (02) :208-212
[2]   Structure of human succinic semialdehyde dehydrogenase gene: identification of promoter region and alternatively processed isoforms [J].
Blasi, P ;
Boyl, PP ;
Ledda, M ;
Novelletto, A ;
Gibson, KM ;
Jakobs, C ;
Hogema, B ;
Akaboshi, S ;
Loreni, F ;
Malaspina, P .
MOLECULAR GENETICS AND METABOLISM, 2002, 76 (04) :348-362
[3]   Cis-acting variation in the expression of a high proportion of genes in human brain [J].
Bray, NJ ;
Buckland, PR ;
Owen, MJ ;
O'Donovan, MC .
HUMAN GENETICS, 2003, 113 (02) :149-153
[4]   Association study designs for complex diseases [J].
Cardon, LR ;
Bell, JI .
NATURE REVIEWS GENETICS, 2001, 2 (02) :91-99
[5]   PURIFICATION FROM HUMAN-BRAIN AND SOME PROPERTIES OF 2 NADPH-LINKED ALDEHYDE REDUCTASES WHICH REDUCE SUCCINIC SEMI-ALDEHYDE TO 4-HYDROXYBUTYRATE [J].
CASH, CD ;
MAITRE, M ;
MANDEL, P .
JOURNAL OF NEUROCHEMISTRY, 1979, 33 (06) :1169-1175
[6]   Two exon-skipping mutations as the molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria) [J].
Chambliss, KL ;
Hinson, DD ;
Trettel, F ;
Malaspina, P ;
Novelletto, A ;
Jakobs, C ;
Gibson, KM .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (02) :399-408
[7]  
Cohen J., 1988, STAT POWER ANAL BEHA
[8]   Role of the cholinergic muscarinic 2 receptor (CHRM2) gene in cognition [J].
Comings, DE ;
Wu, S ;
Rostamkhani, M ;
McGue, M ;
Iacono, WG ;
Cheng, LSC ;
MacMurray, JP .
MOLECULAR PSYCHIATRY, 2003, 8 (01) :10-11
[9]   Mechanism for the learning deficits in a mouse model of neurofibromatosis type 1 [J].
Costa, RM ;
Federov, NB ;
Kogan, JH ;
Murphy, GG ;
Stern, J ;
Ohno, M ;
Kucherlapati, R ;
Jacks, T ;
Silva, AJ .
NATURE, 2002, 415 (6871) :526-530
[10]   Trace fear conditioning involves hippocampal α5 GABAA receptors [J].
Crestani, F ;
Keist, R ;
Fritschy, JM ;
Benke, D ;
Vogt, K ;
Prut, L ;
Blüthmann, H ;
Möhler, H ;
Rudolph, U .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (13) :8980-8985