A high proportion of chromosome 21 promoter polymorphisms influence transcriptional activity

被引:20
作者
Buckland, PR [1 ]
Coleman, SL [1 ]
Hoogendoorn, B [1 ]
Guy, C [1 ]
Smith, SK [1 ]
O'Donovan, MC [1 ]
机构
[1] Cardiff Univ, Coll Med, Dept Psychol Med, Cardiff CF14 4XN, S Glam, Wales
来源
GENE EXPRESSION-THE JOURNAL OF LIVER RESEARCH | 2003年 / 11卷 / 5-6期
基金
英国医学研究理事会;
关键词
CRYAA; cataracts; IFNAR1; galactosyltransferase; KCNJ15; down syndrome; NCAM2; B3GALT5; hepatitis C;
D O I
10.3727/000000003783992225
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have sought to obtain an unbiased estimate of the proportion of polymorphisms in promoters of human genes that have functional effects. We carried out polymorphism discovery on a randomly selected group of 5 1 gene promoters mapping to human chromosome 21 and successfully analyzed the effect on transcription of 38 of the sequence variants. To achieve this, a total of 53 different haplotypes from 20 promoters were cloned into a modified pGL3 luciferase reporter gene vector and were tested for their abilities to promote transcription in HEK293t and JEG-3 cells. Up to seven (18%) of the 38 tested variants altered transcription by 1.5-fold, confirming that a surprisingly high proportion of promoter region polymorphisms are likely to be functionally important. The functional variants were distributed across the promoters of CRYAA IFNAR1, KCNJ15, NCAM2, IGSF5, and B3GALT5. Three of the genes (NCAM2, IFNAR1, and CRYAA) have been previously associated with human phenotypes and the polymorphisms we describe here may therefore play a role in those phenotypes.
引用
收藏
页码:233 / 239
页数:7
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