Transcription of the IL10 gene reveals allele-specific regulation at the mRNA level

被引:69
作者
Kurreeman, FAS
Schonkeren, JJM
Heijmans, BT
Toes, REM
Huizinga, TWJ
机构
[1] Leiden Univ, Med Ctr, Dept Rheumatol, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Mol Epidemiol, NL-2300 RA Leiden, Netherlands
关键词
D O I
10.1093/hmg/ddh187
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
Interleukin-10 (IL10) is a cytokine with key regulatory and anti-inflammatory function involved in the pathogenesis of various diseases. Although the large interindividual differences in the production of IL10 have been extensively associated with polymorphisms and haplotypes of the IL10 gene, surprisingly little evidence exists that this variation is actually dictated by IL10 haplotypes. Using the technique of allele-specific transcript quantification, the ratio between two alleles (A and G) of the IL10 gene was characterized in 15 healthy heterozygous individuals. Two groups were identified whereby donors in group 1 exhibited a 1 : 1 ratio, whereas those in group 2 exhibited a ratio>1 (P<0.0017). We found that donors heterozygous for haplotype IL10.2 (one of the four ancient IL10 haplotypes) were only prevalent in the group that showed higher allelic expression ratios. In this study we show that IL10 alleles are indeed differentially transcribed in cells from heterozygous individuals and that IL10 haplotypes dictate production of IL10. These findings show that interindividual differences in IL10 protein levels can be explained at the transcriptional level.
引用
收藏
页码:1755 / 1762
页数:8
相关论文
共 23 条
[1]   GOLD - Graphical Overview of Linkage Disequilibrium [J].
Abecasis, GR ;
Cookson, WOC .
BIOINFORMATICS, 2000, 16 (02) :182-183
[2]   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
[3]   Detection of regulatory variation in mouse genes [J].
Cowles, CR ;
Hirschhorn, JN ;
Altshuler, D ;
Lander, ES .
NATURE GENETICS, 2002, 32 (03) :432-437
[4]   Frequency of functional interleukin-10 promoter polymorphism is different between relapse-onset and primary progressive multiple sclerosis [J].
de Jong, BA ;
Westendorp, RGJ ;
Eskdale, J ;
Uitdehaag, BMJ ;
Huizinga, TWJ .
HUMAN IMMUNOLOGY, 2002, 63 (04) :281-285
[5]  
de Waal MR, 1991, J EXP MED, V174, P1209
[6]   Unravelling heterochromatin: competition between positive and negative factors regulates accessibility [J].
Dillon, N ;
Festenstein, R .
TRENDS IN GENETICS, 2002, 18 (05) :252-258
[7]   Microsatellite alleles and single nucleotide polymorphisms (SNP) combine to form four major haplotype families at the human interleukin-10 (IL-10) locus [J].
Eskdale, J ;
Keijsers, V ;
Huizinga, T ;
Gallagher, G .
GENES AND IMMUNITY, 1999, 1 (02) :151-155
[8]   Interleukin 10 secretion in relation to human IL-10 locus haplotypes [J].
Eskdale, J ;
Gallagher, G ;
Verweij, CL ;
Keijsers, V ;
Westendorp, RGJ ;
Huizinga, TWJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (16) :9465-9470
[9]   The structure of haplotype blocks in the human genome [J].
Gabriel, SB ;
Schaffner, SF ;
Nguyen, H ;
Moore, JM ;
Roy, J ;
Blumenstiel, B ;
Higgins, J ;
DeFelice, M ;
Lochner, A ;
Faggart, M ;
Liu-Cordero, SN ;
Rotimi, C ;
Adeyemo, A ;
Cooper, R ;
Ward, R ;
Lander, ES ;
Daly, MJ ;
Altshuler, D .
SCIENCE, 2002, 296 (5576) :2225-2229
[10]   Novel single nucleotide polymorphisms in the distal IL-10 promoter affect IL-10 production and enhance the risk of systemic lupus erythematosus [J].
Gibson, AW ;
Edberg, JC ;
Wu, JM ;
Westendorp, RGJ ;
Huizinga, TWJ ;
Kimberly, RP .
JOURNAL OF IMMUNOLOGY, 2001, 166 (06) :3915-3922