Two single nucleotide polymorphisms (SNPs) in the CALL gene for association studies with IQ

被引:11
作者
Angeloni, D [1 ]
Wei, MH [1 ]
Lerman, MI [1 ]
机构
[1] NCI, Immunobiol Lab, Frederick Canc Res & Dev Ctr, Frederick, MD 21702 USA
关键词
CALL; CEPH; IQ; SNPs; SSCP; 3p-sundrome;
D O I
10.1097/00041444-199909000-00011
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A number of genes underlie the molecular bases of intelligence. Among these is probably CALL, a novel member of the L1 gene family of neural cell adhesion molecules. By using the single strand conformation polymorphism (SSCP) protocol, we screened the regions of the CALL gene corresponding to the 5' and 3' untranslated regions (UTRs) of the CALL mRNA, searching for polymorphisms that could be useful in association studies in the field of intelligence. We report the finding of T-to-A and T-to-C single nucleotide polymorphisms (SNPs) in the 3' UTR of CALL. These SNPs have an index of heterozygosity of 0.13 and 0.10, respectively, Research is in progress to understand the association between these variants and high IQ. (C) 1999 Lippincott Williams & Wilkins.
引用
收藏
页码:165 / 167
页数:3
相关论文
共 14 条
[1]  
Angeloni D, 1999, AM J MED GENET, V86, P482, DOI 10.1002/(SICI)1096-8628(19991029)86:5<482::AID-AJMG15>3.0.CO
[2]  
2-L
[3]   A quantitative trait locus associated with cognitive ability in children [J].
Chorney, MJ ;
Chorney, K ;
Seese, N ;
Owen, MJ ;
Daniels, J ;
McGuffin, P ;
Thompson, LA ;
Detterman, DK ;
Benbow, C ;
Lubinski, D ;
Eley, T ;
Plomin, R .
PSYCHOLOGICAL SCIENCE, 1998, 9 (03) :159-166
[4]  
Daniels J, 1998, HUM BIOL, V70, P281
[5]   PROGRAM DESCRIPTION - CENTER-DETUDE-DU-POLYMORPHISME-HUMAIN (CEPH) - COLLABORATIVE GENETIC-MAPPING OF THE HUMAN GENOME [J].
DAUSSET, J ;
CANN, H ;
COHEN, D ;
LATHROP, M ;
LALOUEL, JM ;
WHITE, R .
GENOMICS, 1990, 6 (03) :575-577
[6]   Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome [J].
Drumheller, T ;
McGillivray, BC ;
Behrner, D ;
MacLeod, P ;
McFadden, DE ;
Roberson, J ;
Venditti, C ;
Chorney, K ;
Chorney, M ;
Smith, DI .
JOURNAL OF MEDICAL GENETICS, 1996, 33 (10) :842-847
[7]   THE DETECTION OF SUBTELOMERIC CHROMOSOMAL REARRANGEMENTS IN IDIOPATHIC MENTAL-RETARDATION [J].
FLINT, J ;
WILKIE, AOM ;
BUCKLE, VJ ;
WINTER, RM ;
HOLLAND, AJ ;
MCDERMID, HE .
NATURE GENETICS, 1995, 9 (02) :132-140
[8]   L1-associated diseases: clinical geneticists divide, molecular geneticists unite [J].
Fransen, E ;
VanCamp, G ;
Vits, L ;
Willems, PJ .
HUMAN MOLECULAR GENETICS, 1997, 6 (10) :1625-1632
[9]   X linked hydrocephalus and MASA syndrome [J].
Kenwrick, S ;
Jouet, M ;
Donnai, D .
JOURNAL OF MEDICAL GENETICS, 1996, 33 (01) :59-65
[10]   The genetics of cognitive abilities and disabilities [J].
Plomin, R ;
DeFries, JC .
SCIENTIFIC AMERICAN, 1998, 278 (05) :62-69