GENOMIC ORGANIZATION OF A MOUSE GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE GENE (GAPD-S) EXPRESSED IN POSTMEIOTIC SPERMATOGENIC CELLS

被引:30
作者
WELCH, JE
BROWN, PR
OBRIEN, DA
EDDY, EM
机构
[1] UNIV N CAROLINA,REPROD BIOL LABS,CHAPEL HILL,NC
[2] UNIV N CAROLINA,DEPT PEDIAT,CHAPEL HILL,NC
[3] UNIV N CAROLINA,DEPT CELL BIOL & ANAT,CHAPEL HILL,NC
来源
DEVELOPMENTAL GENETICS | 1995年 / 16卷 / 02期
关键词
SPERMATOGENESIS; GLYCOLYSIS; GENE EXPRESSION; ENZYME; GLYCERALDEHYDE 3-PHOSPHATE DEHYDROGENASE;
D O I
10.1002/dvg.1020160210
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Gapd-s gene encodes an isoform of the glyceraldehyde 3-phosphate dehydrogenase enzyme expressed only in post-meiotic spermatogenic cells. Two clones containing the Gapd-s gene were isolated from a mouse genomic library. Sequencing and restriction enzyme analysis demonstrated that this single-copy gene contains 11 exons and spans 9596 base pairs. The locations of Gapd-s exons and introns are conserved when compared to the corresponding portions of the chicken and human somatic Gapd genes. The promoter region contains no TATA box, although there is a potential SP1 recognition site within exon 1. Like other TATA-less genes, primer extension analysis reveals some heterogeneity in the site of transcription initiation with Gapd-s transcripts initiating from three discrete sites. Northern analysis demonstrated that a 1.5-kb Gapd-s mRNA is expressed in the testis in at least three mammalian orders, indicating that the Gapd-s gene appeared early in mammalian evolution. Using GAPD-deficient bacteria, mouse GAPD-S was shown to be capable of functioning as a glycolytic enzyme. Since GAPD has been proposed to be a key enzyme regulating glycolysis in spermatogenic cells, GAPD-S may represent a potential target for toxicological or contraceptive agents affecting fertility by interfering with glycolysis. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:179 / 189
页数:11
相关论文
共 47 条
[1]  
Ausubel FM, 1987, CURRENT PROTOCOLS MO, V1-5
[2]   A GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE PSEUDOGENE ON THE SHORT ARM OF THE HUMAN X-CHROMOSOMES DEFINES A MULTIGENE FAMILY [J].
BENHAM, FJ ;
HODGKINSON, S ;
DAVIES, KE .
EMBO JOURNAL, 1984, 3 (11) :2635-2640
[3]   SCREENING GAMMAGT RECOMBINANT CLONES BY HYBRIDIZATION TO SINGLE PLAQUES INSITU [J].
BENTON, WD ;
DAVIS, RW .
SCIENCE, 1977, 196 (4286) :180-182
[4]   THE TESTIS-SPECIFIC PHOSPHOGLYCERATE KINASE GENE PGK-2 IS A RECRUITED RETROPOSON [J].
BOER, PH ;
ADRA, CN ;
LAU, YF ;
MCBURNEY, MW .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (09) :3107-3112
[5]  
BRUNS G, 1979, CYTOGENET CELL GENET, V25, P139
[6]  
BUEHR M, 1981, J REPROD FERTIL, V63, P169, DOI 10.1530/jrf.0.0630169
[7]   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
[8]   MULTIPLE CONTROL ELEMENTS REGULATE TRANSCRIPTION FROM THE MOST DISTAL PROMOTER OF HUMAN ALDOLASE-A GENE [J].
COSTANZO, P ;
LUPO, A ;
RIPPA, E ;
GROSSO, M ;
SALVATORE, F ;
IZZO, P .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 195 (02) :935-944
[9]  
CURTIS H, 1977, BIOLOGY
[10]   A TESTIS-SPECIFIC FORM OF THE HUMAN PYRUVATE-DEHYDROGENASE E1-ALPHA SUBUNIT IS CODED FOR BY AN INTRONLESS GENE ON CHROMOSOME-4 [J].
DAHL, HHM ;
BROWN, RM ;
HUTCHISON, WM ;
MARAGOS, C ;
BROWN, GK .
GENOMICS, 1990, 8 (02) :225-232