A HUMAN ALCOHOL-DEHYDROGENASE GENE (ADH6) ENCODING AN ADDITIONAL CLASS OF ISOZYME

被引:95
作者
YASUNAMI, M [1 ]
CHEN, CS [1 ]
YOSHIDA, A [1 ]
机构
[1] CITY HOPE NATL MED CTR, BECKMAN RES INT, 1450 E DUARTE RD, DUARTE, CA 91010 USA
关键词
D O I
10.1073/pnas.88.17.7610
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The human alcohol dehydrogenase (ADH; alcohol:NAD+ oxidoreductase, EC 1.1.1.1) gene family consists of five known loci (ADH1-ADH5), which have been mapped close together on chromosome 4 (4q21-25). ADH isozymes encoded by these genes are grouped in three distinct classes in terms of their enzymological properties. A moderate structural similarity is observed between the members of different classes. We isolated an additional member of the ADH gene family by means of cross-hybridization with the ADH2 (class I) cDNA probe. cDNA clones corresponding lo this gene were derived from PCR-amplified libraries as well. The coding sequence of a 368-amino-acid-long open reading frame was interrupted by introns into eight exons and spanned approximately 17 kilobases on the genome. The gene contains a glucocorticoid response element at the 5' region. The transcript was detected in the stomach and liver. The deduced amino acid sequence of the open reading frame showed about 60% positional identity with known human ADHs. This extent of homology is comparable to interclass similarity in the human ADH family. Thus, the newly identified gene, which is designated ADH6, governs the synthesis of an enzyme that belongs to another class of ADHs presumably with a distinct physiological role.
引用
收藏
页码:7610 / 7614
页数:5
相关论文
共 26 条
[1]   IMMUNOLOGICAL AND BIOCHEMICAL-CHARACTERIZATION OF THE HUMAN ALCOHOL-DEHYDROGENASE CHI-ADH ISOZYME [J].
ADINOLFI, A ;
ADINOLFI, M ;
HOPKINSON, DA .
ANNALS OF HUMAN GENETICS, 1984, 48 (JAN) :1-10
[2]  
DUESTER G, 1986, J BIOL CHEM, V261, P2027
[3]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[4]   HIGH BLOOD-ALCOHOL LEVELS IN WOMEN - THE ROLE OF DECREASED GASTRIC ALCOHOL-DEHYDROGENASE ACTIVITY AND 1ST-PASS METABOLISM [J].
FREZZA, M ;
DIPADOVA, C ;
POZZATO, G ;
TERPIN, M ;
BARAONA, E ;
LIEBER, CS .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (02) :95-99
[5]   RAPID PRODUCTION OF FULL-LENGTH CDNAS FROM RARE TRANSCRIPTS - AMPLIFICATION USING A SINGLE GENE-SPECIFIC OLIGONUCLEOTIDE PRIMER [J].
FROHMAN, MA ;
DUSH, MK ;
MARTIN, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) :8998-9002
[6]   OCULAR NAD-DEPENDENT ALCOHOL-DEHYDROGENASE AND ALDEHYDE DEHYDROGENASE IN THE BABOON [J].
HOLMES, RS ;
VANDEBERG, JL .
EXPERIMENTAL EYE RESEARCH, 1986, 43 (03) :383-396
[7]  
HSU LC, 1989, AM J HUM GENET, V45, P196
[8]   3 HUMAN ALCOHOL-DEHYDROGENASE SUBUNITS - CDNA STRUCTURE AND MOLECULAR AND EVOLUTIONARY DIVERGENCE [J].
IKUTA, T ;
SZETO, S ;
YOSHIDA, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (03) :634-638
[9]   MOLECULAR-CLONING OF A FULL-LENGTH CDNA FOR HUMAN ALCOHOL-DEHYDROGENASE [J].
IKUTA, T ;
FUJIYOSHI, T ;
KURACHI, K ;
YOSHIDA, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (09) :2703-2707
[10]   COOPERATIVITY OF GLUCOCORTICOID RESPONSE ELEMENTS LOCATED FAR UPSTREAM OF THE TYROSINE AMINOTRANSFERASE GENE [J].
JANTZEN, HM ;
STRAHLE, U ;
GLOSS, B ;
STEWART, F ;
SCHMID, W ;
BOSHART, M ;
MIKSICEK, R ;
SCHUTZ, G .
CELL, 1987, 49 (01) :29-38