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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
来源:
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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页码:408 / 416
页数:9
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