Mouse hexokinase II gene:: structure, cDNA, promoter analysis, and expression pattern

被引:31
作者
Heikkinen, S [1 ]
Suppola, S
Malkki, M
Deeb, SS
Jänne, J
Laakso, M
机构
[1] Univ Kuopio, Dept Med, FIN-70211 Kuopio, Finland
[2] Univ Kuopio, AI Virtanen Inst Mol Sci, FIN-70211 Kuopio, Finland
[3] Univ Washington, Dept Med, Seattle, WA 98195 USA
[4] Univ Washington, Dept Genet, Seattle, WA 98195 USA
关键词
D O I
10.1007/s003350010019
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 mammalian tissues, the phosphorylation of intracellular glucose to glucose-6-phosphate (Glu-6-P) is facilitated by four distinct hexokinase (HK) isoenzymes, designated as HKI-IV. Because of the role of HKII as a leading glycolytic enzyme in insulin-sensitive tissues such as skeletal muscle, heart, and adipose tissue, defects in HKII function could contribute to the development of insulin resistance and perhaps Type 2 diabetes. As a first step towards elucidation of the physiological role of HKII in insulin resistance and type 2 diabetes using mouse knock-out models, we determined the genomic structure, sequence of the cDNA and of 4.8 kb of the 5' regulatory region, and tissue-specific expression of the mouse HKII gene. The gene comprises 18 exons that span approximately 50 kb of DNA. Nucleotide sequence of the proximal promoter revealed a number of conserved putative transcription factor binding motifs. We also found numerous repeat elements throughout the mouse HKII gene. The mouse HKII cDNA is approximately 5.5 kb in length and contains an open reading frome of 2751 bp encoding a protein of 917 amino acids. The mouse HKII gene is predominantly expressed in skeletal muscle, heart, and adipose tissue. The transcription initiation and polyadenylation sites for the mouse HKII mRNA were similar to those of the rat and human genes.
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页码:91 / 96
页数:6
相关论文
共 36 条
[21]   The structure of mammalian hexokinase-1 [J].
Mulichak, AM ;
Wilson, JE ;
Padmanabhan, K ;
Garavito, RM .
NATURE STRUCTURAL BIOLOGY, 1998, 5 (07) :555-560
[22]   Identification of the cDNA for human red blood cell-specific hexokinase isozyme [J].
Murakami, K ;
Piomelli, S .
BLOOD, 1997, 89 (03) :762-766
[23]   REGULATION OF HEXOKINASE-II GENE-TRANSCRIPTION AND GLUCOSE PHOSPHORYLATION BY CATECHOLAMINES, CYCLIC-AMP, AND INSULIN [J].
OSAWA, H ;
PRINTZ, RL ;
WHITESELL, RR ;
GRANNER, DK .
DIABETES, 1995, 44 (12) :1426-1432
[24]   Identification and characterization of basal and cyclic AMP response elements in the promoter of the rat hexokinase II genes [J].
Osawa, H ;
Robey, RB ;
Printz, RL ;
Granner, DK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (29) :17296-17303
[25]   THE EFFECTS OF HYPERINSULINEMIA AND HYPERGLYCEMIA ON GLUT4 AND HEXOKINASE-II MESSENGER-RNA AND PROTEIN IN RAT SKELETAL-MUSCLE AND ADIPOSE-TISSUE [J].
POSTIC, C ;
LETURQUE, A ;
RENCUREL, F ;
PRINTZ, RL ;
FOREST, C ;
GRANNER, DK ;
GIRARD, J .
DIABETES, 1993, 42 (06) :922-929
[26]   DEVELOPMENT AND REGULATION OF GLUCOSE-TRANSPORTER AND HEXOKINASE EXPRESSION IN RAT [J].
POSTIC, C ;
LETURQUE, A ;
PRINTZ, RL ;
MAULARD, P ;
LOIZEAU, M ;
GRANNER, DK ;
GIRARD, J .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (04) :E548-E559
[27]   HUMAN HEXOKINASE-II MESSENGER-RNA AND GENE STRUCTURE [J].
PRINTZ, RL ;
ARDEHALI, H ;
KOCH, S ;
GRANNER, DK .
DIABETES, 1995, 44 (03) :290-294
[28]  
PRINTZ RL, 1993, J BIOL CHEM, V268, P5209
[29]   Alu: Structure, origin, evolution, significance, and function of one-tenth of human DNA [J].
Schmid, CW .
PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, VOL 53, 1996, 53 :283-319
[30]   Assignment of hexokinase types 1,2,3 (Hk1,2,3) and glucokinase (Gck) to rat chromosome band 20q11, 4q34, 17q12 and 14q21 respectively, by in situ hybridization [J].
Sebastian, S ;
Hoebee, B ;
Hande, MP ;
Kenkare, UW ;
Natarajan, AT .
CYTOGENETICS AND CELL GENETICS, 1997, 77 (3-4) :266-267