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.
引用
收藏
页码:408 / 416
页数:9
相关论文
共 50 条
[21]   REPAIR OF PREMUTAGENIC DNA LESIONS IN HUMAN-FETAL TISSUES - EVIDENCE FOR LOW-LEVELS OF O-6-METHYLGUANINE-DNA METHYLTRANSFERASE AND URACIL-DNA GLYCOSYLASE ACTIVITY IN SOME TISSUES [J].
KROKAN, H ;
HAUGEN, A ;
MYRNES, B ;
GUDDAL, PH .
CARCINOGENESIS, 1983, 4 (12) :1559-1564
[22]   SEQUENCE CONSERVATION IN ALU EVOLUTION [J].
LABUDA, D ;
STRIKER, G .
NUCLEIC ACIDS RESEARCH, 1989, 17 (07) :2477-2491
[23]   CPG ISLANDS AS GENE MARKERS IN THE HUMAN GENOME [J].
LARSEN, F ;
GUNDERSEN, G ;
LOPEZ, R ;
PRYDZ, H .
GENOMICS, 1992, 13 (04) :1095-1107
[24]   PHYLOGENETIC EVIDENCE FOR MULTIPLE ALU SOURCE GENES [J].
LEEFLANG, EP ;
LIU, WM ;
HASHIMOTO, C ;
CHOUDARY, PV ;
SCHMID, CW .
JOURNAL OF MOLECULAR EVOLUTION, 1992, 35 (01) :7-16
[25]   N-GLYCOSIDASE FROM ESCHERICHIA-COLI THAT RELEASES FREE URACIL FROM DNA CONTAINING DEAMINATED CYTOSINE RESIDUES [J].
LINDAHL, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1974, 71 (09) :3649-3653
[26]   PROPOSED ROLES FOR DNA METHYLATION IN ALU TRANSCRIPTIONAL REPRESSION AND MUTATIONAL INACTIVATION [J].
LIU, WM ;
SCHMID, CW .
NUCLEIC ACIDS RESEARCH, 1993, 21 (06) :1351-1359
[27]   SP1 SITES IN THE MOUSE APRT GENE PROMOTER ARE REQUIRED TO PREVENT METHYLATION OF THE CPG ISLAND [J].
MACLEOD, D ;
CHARLTON, J ;
MULLINS, J ;
BIRD, AP .
GENES & DEVELOPMENT, 1994, 8 (19) :2282-2292
[28]   A TRANSPOSITIONALLY AND TRANSCIPTIONALLY COMPETENT ALU SUBFAMILY [J].
MATERA, AG ;
HELLMANN, U ;
SCHMID, CW .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (10) :5424-5432
[29]   PROLIFERATING CELL NUCLEAR ANTIGEN-DEPENDENT ABASIC SITE REPAIR IN XENOPUS-LAEVIS OOCYTES - AN ALTERNATIVE PATHWAY OF BASE EXCISION DNA-REPAIR [J].
MATSUMOTO, Y ;
KIM, K ;
BOGENHAGEN, DF .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (09) :6187-6197
[30]   EXPRESSED GENES, ALU REPEATS AND POLYMORPHISMS IN COSMIDS SEQUENCED FROM CHROMOSOME-4P16.3 [J].
MCCOMBIE, WR ;
MARTINGALLARDO, A ;
GOCAYNE, JD ;
FITZGERALD, M ;
DUBNICK, M ;
KELLEY, JM ;
CASTILLA, L ;
LIU, LI ;
WALLACE, S ;
TRAPP, S ;
TAGLE, D ;
WHALEY, WL ;
CHENG, S ;
GUSELLA, J ;
FRISCHAUF, AM ;
POUSTKA, A ;
LEHRACH, H ;
COLLINS, FS ;
KERLAVAGE, AR ;
FIELDS, C ;
VENTER, JC .
NATURE GENETICS, 1992, 1 (05) :348-353