Human growth hormone 1 (GH1) gene expression:: Complex haplotype dependent influence of polymorphic variation in the proximal promoter and locus control region

被引:83
作者
Horan, M
Millar, DS
Hedderich, J
Lewis, G
Newsway, V
Mo, N
Fryklund, L
Procter, AM
Krawczak, M
Cooper, DN
机构
[1] Univ Wales Coll Med, Inst Med Genet, Cardiff CF14 4XN, S Glam, Wales
[2] Univ Kiel, Inst Med Informat & Stat, Kiel, Germany
[3] Pharm AB, Stockholm, Sweden
关键词
growth hormone; GH1; promoter; polymorphism; SNP; haplotypes; expression; transcription factor binding; haplotype partitioning; locus control region; short stature; linkage disequilibrium; evolution;
D O I
10.1002/humu.10167
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The proximal promoter region of the human pituitary expressed growth hormone (GH1) gene is highly polymorphic, containing at least 15 single nucleotide polymorphisms (SNPs). This variation is manifest in 40 different haplotypes, the high diversity being explicable in terms of gene conversion, recurrent mutation, and selection. Functional analysis showed that 12 haplotypes were associated with a significantly reduced level of reporter gene expression whereas 10 haplotypes were associated with a significantly increased level. The former tend to be more prevalent in the general population than the latter (p<0.01), possibly as a consequence of selection. Although individual SNPs contributed to promoter strength in a highly interactive and non-additive fashion, haplotype partitioning was successful in identifying six SNPs as major determinants of GH1 gene expression. The prediction and functional testing of hitherto unobserved super-maximal and sub-minimal promoter haplotypes was then used to test the efficacy of the haplotype partitioning approach. Electrophoretic mobility shift assays demonstrated that five SNP sites exhibit allele-specific protein binding. An association was noted between adult height and the mean in vitro expression value corresponding to an individual's GH1 promoter haplotype combination (p=0.028) although only 3.3% of the variance of adult height was found to be explicable by reference to this parameter. Three additional SNPs, identified within sites I and II of the upstream locus control region (LCR), were ascribed to three distinct LCR haplotypes. A series of LCR GH1 proximal promoter constructs were used to demonstrate that 1) the LCR enhanced proximal promoter activity by up to 2.8-fold depending upon proximal promoter haplotype, and that 2) the activity of a given proximal promoter haplotype was also differentially enhanced by different LCR haplotypes. The genetic basis of inter individual differences in GH1 gene expression thus appears to be extremely complex. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:408 / 423
页数:16
相关论文
共 53 条
[1]   High-affinity binding sites to the vitamin D receptor DNA binding domain in the human growth hormone promoter [J].
Alonso, M ;
Segura, C ;
Dieguez, C ;
Perez-Fernandez, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 247 (03) :882-887
[2]   The relative power of SNPs and haplotype as genetic markers for association tests [J].
Bader, JS .
PHARMACOGENOMICS, 2001, 2 (01) :11-24
[3]   MEASUREMENT OF GROWTH-HORMONE SYNTHESIS BY RAT PITUITARY CELLS IN CULTURE [J].
BANCROFT, FC .
ENDOCRINOLOGY, 1973, 92 (04) :1014-1021
[4]  
BANDELT HJ, 1995, GENETICS, V141, P743
[5]   DISRUPTION OF A BINDING-SITE FOR HEPATOCYTE NUCLEAR FACTOR-1 IN THE PROTEIN-C GENE PROMOTER IS ASSOCIATED WITH HEREDITARY THROMBOPHILIA [J].
BERG, LP ;
SCOPES, DA ;
ALHAQ, A ;
KAKKAR, VV ;
COOPER, DN .
HUMAN MOLECULAR GENETICS, 1994, 3 (12) :2147-2152
[6]   A PITUITARY-SPECIFIC TRANS-ACTING FACTOR CAN STIMULATE TRANSCRIPTION FROM THE GROWTH-HORMONE PROMOTER IN EXTRACTS OF NONEXPRESSING CELLS [J].
BODNER, M ;
KARIN, M .
CELL, 1987, 50 (02) :267-275
[7]   The essence of SNPs [J].
Brookes, AJ .
GENE, 1999, 234 (02) :177-186
[8]   Polymorphisms in the human paraoxonase (PON1) promoter [J].
Brophy, VH ;
Hastings, MD ;
Clendenning, JB ;
Richter, RJ ;
Jarvik, GP ;
Furlong, CE .
PHARMACOGENETICS, 2001, 11 (01) :77-84
[9]  
Chatterjee Satipati, 1999, Applied Human Science, V18, P1, DOI 10.2114/jpa.18.1
[10]   THE HUMAN GROWTH-HORMONE LOCUS - NUCLEOTIDE-SEQUENCE, BIOLOGY, AND EVOLUTION [J].
CHEN, EY ;
LIAO, YC ;
SMITH, DH ;
BARRERASALDANA, HA ;
GELINAS, RE ;
SEEBURG, PH .
GENOMICS, 1989, 4 (04) :479-497