The two most common alleles of the coding GGN repeat in the androgen receptor gene cause differences in protein function

被引:28
作者
Brockschmidt, Felix F. [1 ]
Noethen, Markus M. [1 ]
Hillmer, Axel M. [1 ]
机构
[1] Univ Bonn, Dept Genom, Life & Brain Ctr, D-53127 Bonn, Germany
关键词
D O I
10.1677/JME-06-0072
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Genetic studies have reported association of a polyglycine-encoding GGN repeat in exon 1 of the androgen receptor (AR) gene with common human traits. The polyglycine tract is located in the transactivating domain of the AR protein, suggesting an effect of repeat length on receptor function. Here, we compare the functional characteristics of the two most common alleles (23 and 24 repeats) and two extreme alleles (110 and 27 repeats) in a reporter gene assay in HeLa cells. A correlation between the repeat length and AR activity was observed. This is attributable to both a higher protein concentration, determined by ELISA, and a higher per-protein activity of long repeat alleles. Interestingly, protein concentration does not correlate with transcript quantity, determined by real-time PCR assays, and no influence of repeat length on protein stability could be detected in translation inhibition assays. This may suggest that repeat length affects translation efficiency. In conclusion, our data provide evidence of functional differences between the two most common alleles of the AR GGN repeat, supporting its potential role in the development of human traits.
引用
收藏
页码:1 / 8
页数:8
相关论文
共 38 条
[21]   Extent of linkage disequilibrium between the androgen receptor gene CAG and GGC repeats in human populations: implications for prostate cancer risk [J].
Kittles, RA ;
Young, D ;
Weinrich, S ;
Hudson, J ;
Argyropoulos, G ;
Ukoli, F ;
Adams-Campbell, L ;
Dunston, GM .
HUMAN GENETICS, 2001, 109 (03) :253-261
[22]   The new genomics: Global views of biology [J].
Lander, ES .
SCIENCE, 1996, 274 (5287) :536-539
[23]   Recent advances in androgen receptor action [J].
Lee, HJ ;
Chang, C .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2003, 60 (08) :1613-1622
[24]   Codon-usage variants in the polymorphic (GGN)(n) trinucleotide repeat of the human androgen receptor gene [J].
Lumbroso, R ;
Beitel, LK ;
Vasiliou, DM ;
Trifiro, MA ;
Pinsky, L .
HUMAN GENETICS, 1997, 101 (01) :43-46
[25]   Functional in vitro characterisation of the androgen receptor GGN polymorphism [J].
Lundin, K. B. ;
Giwercman, A. ;
Dizeyi, N. ;
Giwercman, Y. L. .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2007, 264 (1-2) :184-187
[26]   Androgen receptor gene GGN repeat length and reproductive characteristics in young Swedish men [J].
Lundin, K. B. ;
Giwercman, Y. L. ;
Rylander, L. ;
Hagmar, L. ;
Giwercman, A. .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2006, 155 (02) :347-354
[27]   THE NUCLEAR RECEPTOR SUPERFAMILY - THE 2ND DECADE [J].
MANGELSDORF, DJ ;
THUMMEL, C ;
BEATO, M ;
HERRLICH, P ;
SCHUTZ, G ;
UMESONO, K ;
BLUMBERG, B ;
KASTNER, P ;
MARK, M ;
CHAMBON, P ;
EVANS, RM .
CELL, 1995, 83 (06) :835-839
[28]   REDUCED TRANSCRIPTIONAL REGULATORY COMPETENCE OF THE ANDROGEN RECEPTOR IN X-LINKED SPINAL AND BULBAR MUSCULAR-ATROPHY [J].
MHATRE, AN ;
TRIFIRO, MA ;
KAUFMAN, M ;
KAZEMIESFARJANI, P ;
FIGLEWICZ, D ;
ROULEAU, G ;
PINSKY, L .
NATURE GENETICS, 1993, 5 (02) :184-188
[29]   A SIMPLE SALTING OUT PROCEDURE FOR EXTRACTING DNA FROM HUMAN NUCLEATED CELLS [J].
MILLER, SA ;
DYKES, DD ;
POLESKY, HF .
NUCLEIC ACIDS RESEARCH, 1988, 16 (03) :1215-1215
[30]   Transcriptional activation by the androgen receptor in X-linked spinal and bulbar muscular atrophy [J].
Nakajima, H ;
Kimura, F ;
Nakagawa, T ;
Furutama, D ;
Shinoda, K ;
Shimizu, A ;
Ohsawa, N .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1996, 142 (1-2) :12-16