Human uracil-DNA glycosylase gene: Sequence organization, methylation pattern, and mapping to chromosome 12q23-q24.1

被引:40
作者
Haug, T [1 ]
Skorpen, F [1 ]
Kvaloy, K [1 ]
Eftedal, I [1 ]
Lund, H [1 ]
Krokan, HE [1 ]
机构
[1] NORWEGIAN UNIV SCI & TECHNOL,FAC MED,UNIGEN CTR MOL BIOL,N-7005 TRONDHEIM,NORWAY
关键词
D O I
10.1006/geno.1996.0485
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
The human uracil-DNA glycosylase gene (UNG) spans approximately 13.5 kb including the promoter. UNG comprises 6 exons and 5 introns and was assigned to chromosome 12q23-q24.1 by radiation hybrid mapping. UNG exhibits typical features of housekeeping genes, including a 5' CpG island of 1.2 kb and a very GC-rich TATA-less promoter containing a number of elements involved in constitutive expression and cell cycle regulation. A smaller CpG island is located just downstream of the gene. Within the 15-kb sequence we identified 16 Alu retroposons, 2 of which contain putative competent RNA polymerase III promoters, 3 copies of medium reiteration frequency repeats, and 1 copy of a mammalian-wide interspersed repetitive element, as well as a 300-bp TA-dinucleotide repeat. In vitro methylation of the UNG promoter strongly reduced promoter activity, but methylation may not be involved in regulation of UNG in vivo since a narrow region of the 5' CpG island comprising the putative transcription factor binding region appears to be invariably methylation-free. (C) 1996 Academic Press, Inc.
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收藏
页码:408 / 416
页数:9
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