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人类尿嘧啶-DNA糖基化酶基因:序列组织、甲基化模式及定位于染色体12q23-q24.1

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

作者信息

Haug T, Skorpen F, Kvaløy K, Eftedal I, Lund H, Krokan H E

机构信息

UNIGEN Center for Molecular Biology, Medical Faculty, Norwegian University of Science and Technology, Trondheim, Norway.

出版信息

Genomics. 1996 Sep 15;36(3):408-16. doi: 10.1006/geno.1996.0485.

Abstract

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.

摘要

人类尿嘧啶-DNA糖基化酶基因(UNG)跨度约13.5 kb,包括启动子。UNG由6个外显子和5个内含子组成,通过辐射杂种图谱定位到12号染色体q23-q24.1区域。UNG表现出管家基因的典型特征,包括一个1.2 kb的5' CpG岛和一个富含GC且无TATA的启动子,该启动子包含许多参与组成型表达和细胞周期调控的元件。一个较小的CpG岛位于该基因的下游。在15 kb的序列中,我们鉴定出16个Alu逆转座子,其中2个含有推定的有活性的RNA聚合酶III启动子,3个中度重复频率重复序列拷贝,1个哺乳动物广泛散布重复元件拷贝,以及一个300 bp的TA二核苷酸重复序列。UNG启动子的体外甲基化强烈降低了启动子活性,但甲基化可能不参与UNG在体内的调控,因为包含推定转录因子结合区域的5' CpG岛的一个狭窄区域似乎始终无甲基化。

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