STRUCTURE OF THE HUMAN GENE FOR ALPHA-ENOLASE

被引:71
作者
GIALLONGO, A [1 ]
OLIVA, D [1 ]
CALI, L [1 ]
BARBA, G [1 ]
BARBIERI, G [1 ]
FEO, S [1 ]
机构
[1] CNR, DIPARTIMENTO BIOL CELLULARE & SVILUPPO, PALERMO, ITALY
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1990年 / 190卷 / 03期
关键词
D O I
10.1111/j.1432-1033.1990.tb15611.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In mammals there are at least three isoforms of the glycolytic enzyme enolase encoded by three similar genes: α, β and γ. In this report we describe the isolation and characterization of the human α‐enolase locus. The gene appears to exist as a single copy in the haploid genome and is composed of 12 exons distributed over more than 18000 bases. The structure of this gene has a high degree of similarity to that of the human and rat γ‐enolase genes, with identical positions for all the intron regions. Primer extension and S1 nuclease protection experiments indicate that transcription is initiated at multiple sites. The putative promoter region, like that of other housekeeping genes, lacks canonical TATA and CAAT boxes, is extremely G + C‐rich and contains several potential SP1 binding sites. Furthermore, various sequences similar to known regulatory elements were detected. Copyright © 1990, Wiley Blackwell. All rights reserved
引用
收藏
页码:567 / 573
页数:7
相关论文
共 38 条
[1]  
Ausubel FM., 1988, CURRENT PROTOCOLS MO
[2]   TRANSCRIPTION TERMINATION AND 3' PROCESSING - THE END IS IN SITE [J].
BIRNSTIEL, ML ;
BUSSLINGER, M ;
STRUB, K .
CELL, 1985, 41 (02) :349-359
[3]   PURIFICATION AND BIOCHEMICAL-CHARACTERIZATION OF THE PROMOTER-SPECIFIC TRANSCRIPTION FACTOR, SPL [J].
BRIGGS, MR ;
KADONAGA, JT ;
BELL, SP ;
TJIAN, R .
SCIENCE, 1986, 234 (4772) :47-52
[4]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[5]   PROMOTER SEQUENCES OF EUKARYOTIC PROTEIN-CODING GENES [J].
CORDEN, J ;
WASYLYK, B ;
BUCHWALDER, A ;
CORSI, PS ;
KEDINGER, C ;
CHAMBON, P .
SCIENCE, 1980, 209 (4463) :1406-1414
[6]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[7]  
FEO S, 1990, IN PRESS SEQUENCE
[8]   LAMBDA-REPLACEMENT VECTORS CARRYING POLYLINKER SEQUENCES [J].
FRISCHAUF, AM ;
LEHRACH, H ;
POUSTKA, A ;
MURRAY, N .
JOURNAL OF MOLECULAR BIOLOGY, 1983, 170 (04) :827-842
[9]   MOLECULAR-CLONING AND NUCLEOTIDE-SEQUENCE OF A FULL-LENGTH CDNA FOR HUMAN ALPHA-ENOLASE [J].
GIALLONGO, A ;
FEO, S ;
MOORE, R ;
CROCE, CM ;
SHOWE, LC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (18) :6741-6745
[10]   ONE FACTOR RECOGNIZES THE LIVER-SPECIFIC ENHANCERS IN ALPHA-1-ANTITRYPSIN AND TRANSTHYRETIN GENES [J].
GRAYSON, DR ;
COSTA, RH ;
XANTHOPOULOS, KG ;
DARNELL, JE .
SCIENCE, 1988, 239 (4841) :786-788