UNIQUE HEXOKINASE MESSENGER-RIBONUCLEIC-ACID LACKING THE PORIN-BINDING DOMAIN ARE DEVELOPMENTALLY EXPRESSED IN MOUSE SPERMATOGENIC CELLS

被引:75
作者
MORI, C
WELCH, JE
FULCHER, KD
OBRIEN, DA
EDDY, EM
机构
[1] NIEHS,LRDT,GAMETE BIOL SECT,POB 1233,C4-01,RES TRIANGLE PK,NC 27709
[2] UNIV N CAROLINA,REPROD BIOL LABS,CHAPEL HILL,NC 27599
[3] UNIV N CAROLINA,DEPT PEDIAT,CHAPEL HILL,NC 27599
[4] UNIV N CAROLINA,DEPT CELL BIOL & ANAT,CHAPEL HILL,NC 27599
关键词
D O I
10.1095/biolreprod49.2.191
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have identified cDNAs representing three hexokinase mRNAs (Hk1-sa, Hk1-sb, Hk1-sc) by screening mouse spermatogenic cell cDNA libraries with a mouse hepatoma cell line hexokinase (Hk1) cDNA [Arora KY, Fanciulli M, Pederson PL. J Biol Chem 1990; 265:6481-6488]. Although all three cDNAs show 99% identity to the somatic Hk1 cDNA sequence throughout most of their coding region, they differ from this sequence at the 5' end. They contain a common spermatogenic cell-specific sequence and a sequence unique to each cDNA immediately 5' to the common domain. However, they lack the porin-binding domain (PBD) present in this region of Hk1, used for binding to a pore-forming protein in the outer mitochondrial membrane. These observations appear to support a model proposed by others for hexokinase gene evolution in mammals. In addition, we found that Hk1-sb has an internal sequence that is not present in Hk1, Hk1-sa, or Hk1-sc. Moreover, Hk1-sa and Hk1-sb transcripts are developmentally expressed in mouse spermatogenic cells. Hk1-sa mRNA is first expressed during meiosis and continues to be present in postmeiotic germ cells, while the more abundant Hk1-sb mRNA is detected only in postmeiotic germ cells. These and other findings suggest that enzymes encoded by Hk1-sa, Hk1-sb, and Hk1-sc are present only in spermatogenic cells.
引用
收藏
页码:191 / 203
页数:13
相关论文
共 51 条
[1]   PORIN INTERACTION WITH HEXOKINASE AND GLYCEROL KINASE - METABOLIC MICROCOMPARTMENTATION AT THE OUTER MITOCHONDRIAL-MEMBRANE [J].
ADAMS, V ;
GRIFFIN, L ;
TOWBIN, J ;
GELB, B ;
WORLEY, K ;
MCCABE, ERB .
BIOCHEMICAL MEDICINE AND METABOLIC BIOLOGY, 1991, 45 (03) :271-291
[2]  
ANDREONE TL, 1989, J BIOL CHEM, V264, P363
[3]  
ARORA KK, 1990, J BIOL CHEM, V265, P6481
[4]   SPERMATOGENIC CELLS OF PREPUBERAL MOUSE - ISOLATION AND MORPHOLOGICAL CHARACTERIZATION [J].
BELLVE, AR ;
CAVICCHIA, JC ;
MILLETTE, CF ;
OBRIEN, DA ;
BHATNAGAR, YM ;
DYM, M .
JOURNAL OF CELL BIOLOGY, 1977, 74 (01) :68-85
[5]   SCREENING GAMMAGT RECOMBINANT CLONES BY HYBRIDIZATION TO SINGLE PLAQUES INSITU [J].
BENTON, WD ;
DAVIS, RW .
SCIENCE, 1977, 196 (4286) :180-182
[6]   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
[7]  
BUEHR M, 1981, J REPROD FERTIL, V63, P169, DOI 10.1530/jrf.0.0630169
[8]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[9]  
EDWARDS YH, 1983, J REPROD FERTIL, V68, P305
[10]  
EM, 1991, ELECTRON MARK, V1, P1