Characterization of the rat carbonic anhydrase II gene structure: Sequence analysis of the 5' flanking region and 3' UTR

被引:4
作者
McGowan, MH
Neubauer, JA
Stolle, CA
机构
[1] UNIV MED & DENT NEW JERSEY,ROBERT WOOD JOHNSON MED SCH,DEPT MED,NEW BRUNSWICK,NJ 08903
[2] UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
关键词
recombinant DNA; splice junctions; polyadenylation signals; 5' flanking sequence; CpG island; tissue expression;
D O I
10.1016/S0378-1119(96)00700-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The rat carbonic anhydrase II gene was characterized and found to be approximately 15.5 kb in length and to contain 7 exons and 6 introns. All intron/exon junction and branch point sequences conform to consensus sequences, and the overall rat CA II genomic structure appears to be conserved upon comparison with mouse, human, and chicken CA II genes. The putative cis-acting elements within the analyzed 1014 bp 5' flanking region include: TATA box, 4 Sp1 binding sites, 2 AP2 sites and putative tissue-specific beta-globin-like repeat elements. A CpG island of approximately 800 bp was identified that begins about 600 bp upstream of exon 1 and extends about 200 bp into intron 1. In the 3' UTR, two polyadenylation signals (AATAAA) are present, the second of which is believed to be utilized. Northern blot analysis reveals that the 1.7 kb rat CA II mRNA is abundantly expressed in adult male brain and kidney, while negligible amounts are detected in heart and liver.
引用
收藏
页码:181 / 188
页数:8
相关论文
共 38 条
[1]   SCREENING GAMMAGT RECOMBINANT CLONES BY HYBRIDIZATION TO SINGLE PLAQUES INSITU [J].
BENTON, WD ;
DAVIS, RW .
SCIENCE, 1977, 196 (4286) :180-182
[2]   CPG-RICH ISLANDS AND THE FUNCTION OF DNA METHYLATION [J].
BIRD, AP .
NATURE, 1986, 321 (6067) :209-213
[3]   TRANSCRIPTION TERMINATION AND 3' PROCESSING - THE END IS IN SITE [J].
BIRNSTIEL, ML ;
BUSSLINGER, M ;
STRUB, K .
CELL, 1985, 41 (02) :349-359
[4]   SUPERCOIL SEQUENCING - A FAST AND SIMPLE METHOD FOR SEQUENCING PLASMID DNA [J].
CHEN, EY ;
SEEBURG, PH .
DNA-A JOURNAL OF MOLECULAR & CELLULAR BIOLOGY, 1985, 4 (02) :165-170
[5]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[6]   THE NUCLEOTIDE-SEQUENCE AND DERIVED AMINO-ACID-SEQUENCE OF CDNA CODING FOR MOUSE CARBONIC ANHYDRASE-II [J].
CURTIS, PJ ;
WITHERS, E ;
DEMUTH, D ;
WATT, R ;
VENTA, PJ ;
TASHIAN, RE .
GENE, 1983, 25 (2-3) :325-332
[7]   3 REGIONS UPSTREAM FROM THE CAP SITE ARE REQUIRED FOR EFFICIENT AND ACCURATE TRANSCRIPTION OF THE RABBIT BETA-GLOBIN GENE IN MOUSE 3T6 CELLS [J].
DIERKS, P ;
VANOOYEN, A ;
COCHRAN, MD ;
DOBKIN, C ;
REISER, J ;
WEISSMANN, C .
CELL, 1983, 32 (03) :695-706
[8]   STRUCTURE AND EXPRESSION OF MAMMALIAN CARBONIC-ANHYDRASES [J].
EDWARDS, Y .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1990, 18 (02) :171-175
[9]   CHARACTERIZATION OF THE GENES ENCODING CARBONIC ANHYDRASE-I OF CHIMPANZEE AND GORILLA - COMPARATIVE-ANALYSIS OF 5' FLANKING ERYTHROID-SPECIFIC PROMOTER SEQUENCES [J].
EPPERLY, BR ;
BERGENHEM, NCH ;
VENTA, PJ ;
TASHIAN, RE .
GENE, 1993, 131 (02) :249-253
[10]  
ERICKSON RP, 1985, BIOCH GENET, V33, P421