The human LGALS3 (galectin-3) gene:: Determination of the gene structure and functional characterization of the promoter

被引:92
作者
Kadrofske, MM [1 ]
Openo, KP [1 ]
Wang, JL [1 ]
机构
[1] Michigan State Univ, Dept Biochem, E Lansing, MI 48824 USA
关键词
galectins; pre-mRNA splicing factor; immediate-early genes; gene structure;
D O I
10.1006/abbi.1997.0447
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
Galectin-3 is a beta-galactoside-specific lectin that is a pre-mRNA splicing factor. Here we report the genomic organization of the human LGALS3 (galectin-3) gene and functional characterization of the promoter. Southern blot analysis of genomic DNA revealed that galectin-3 is coded by a single gene in the human genome, The gene is composed of six exons and five introns, spanning a total of similar to 17 kilobases (kb), Based on primer extension and ribonuclease protection analyses, there are two transcription initiation sites located 52 and 50 nucleotides (nt) upstream of the exon I-intron 1 border, and defined here as + 1a and + 1b, respectively. The translation start site is in exon II, The ribonucleoprotein like N-terminal domain, containing the proline-glycine-alanine-tyrosine (PGAY) repeat motif, is found entirely within exon III. The carbohydrate recognition sequence is found entirely within exon V. Genomic fragments encompassing -836 to +141 nt (relative to +1a) have significant promoter activity when linked to the luciferase reporter gene and transiently transfected into HeLa cells or human diploid fibroblasts, Quiescent fibroblasts have low promoter activity but the activity increases 100-fold following serum addition, Serum responsive activation regions in the promoter are located between -513 and -339 nt and between -339 and -229 nt; an additional activation region may be located between -105 and -15 nt, Because galectin-3 is an immediate-early gene whose expression is dependent on the proliferative state of the cell, this study provides the basis for determining the molecular mechanisms of transcriptional regulation in neoplasia or cellular senescence. (C) 1998 Academic Press.
引用
收藏
页码:7 / 20
页数:14
相关论文
共 57 条
[1]  
AGRWAL N, 1989, J BIOL CHEM, V264, P17236
[2]  
Ausubel F.M., 1992, SHORT PROTOCOLS MOL, V2nd
[3]   THE PROTEIN ID - A NEGATIVE REGULATOR OF HELIX-LOOP-HELIX DNA-BINDING PROTEINS [J].
BENEZRA, R ;
DAVIS, RL ;
LOCKSHON, D ;
TURNER, DL ;
WEINTRAUB, H .
CELL, 1990, 61 (01) :49-59
[4]   CORRESPONDENCE BETWEEN A MAMMALIAN SPLICEOSOME COMPONENT AND AN ESSENTIAL YEAST SPLICING FACTOR [J].
BENNETT, M ;
REED, R .
SCIENCE, 1993, 262 (5130) :105-108
[5]   OVALBUMIN GENE - EVIDENCE FOR A LEADER SEQUENCE IN MESSENGER-RNA AND DNA SEQUENCES AT EXON-INTRON BOUNDARIES [J].
BREATHNACH, R ;
BENOIST, C ;
OHARE, K ;
GANNON, F ;
CHAMBON, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (10) :4853-4857
[6]   The CREB family of transcription activators [J].
Brindle, Paul K. ;
Montminy, Marc R. .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1992, 2 (02) :199-204
[7]   EFFECTIVE AMPLIFICATION OF LONG TARGETS FROM CLONED INSERTS AND HUMAN GENOMIC DNA [J].
CHENG, S ;
FOCKLER, C ;
BARNES, WM ;
HIGUCHI, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (12) :5695-5699
[8]   MOLECULAR-CLONING OF A HUMAN MACROPHAGE LECTIN SPECIFIC FOR GALACTOSE [J].
CHERAYIL, BJ ;
CHAITOVITZ, S ;
WONG, C ;
PILLAI, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (18) :7324-7328
[9]   STRUCTURE AND EXPRESSION OF THE NEGATIVE GROWTH-FACTOR MOUSE BETA-GALACTOSIDE BINDING-PROTEIN GENE [J].
CHIARIOTTI, L ;
WELLS, V ;
BRUNI, CB ;
MALLUCCI, L .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1089 (01) :54-60
[10]   CHANGES IN GENE-EXPRESSION DURING SENESCENCE IN CULTURE [J].
CRISTOFALO, VJ ;
PIGNOLO, RJ ;
CIANCIARULO, FL ;
DIPAOLO, BR ;
ROTENBERG, MO .
EXPERIMENTAL GERONTOLOGY, 1992, 27 (04) :429-432