THE P450 SUPERFAMILY - UPDATE ON NEW SEQUENCES, GENE-MAPPING, ACCESSION NUMBERS, EARLY TRIVIAL NAMES OF ENZYMES, AND NOMENCLATURE

被引:1687
作者
NELSON, DR
KAMATAKI, T
WAXMAN, DJ
GUENGERICH, FP
ESTABROOK, RW
FEYEREISEN, R
GONZALEZ, FJ
COON, MJ
GUNSALUS, IC
GOTOH, O
OKUDA, K
NEBERT, DW
机构
[1] UNIV CINCINNATI, MED CTR,DEPT ENVIRONM HLTH, CINCINNATI, OH 45267 USA
[2] UNIV CINCINNATI, MED CTR,CTR ENVIRONM GENET, CINCINNATI, OH 45267 USA
[3] UNIV N CAROLINA, DEPT BIOCHEM & BIOPHYS, CHAPEL HILL, NC 27599 USA
[4] HOKKAIDO UNIV, FAC PHARMACEUT SCI, SAPPORO, HOKKAIDO 060, JAPAN
[5] HARVARD UNIV, SCH MED,DEPT BIOL CHEM & MOLEC PHARMACOL, BOSTON, MA 02115 USA
[6] HARVARD UNIV, SCH MED,DANA FARBER CANC INST, BOSTON, MA 02115 USA
[7] VANDERBILT UNIV, MED CTR,SCH MED,DEPT BIOCHEM, NASHVILLE, TN 37232 USA
[8] VANDERBILT UNIV, MED CTR,SCH MED,CTR MOLEC TOXICOL, NASHVILLE, TN 37232 USA
[9] UNIV TEXAS, SW MED CTR,DEPT BIOCHEM, DALLAS, TX 75235 USA
[10] UNIV ARIZONA, DEPT ENTOMOL, TUCSON, AZ 85721 USA
[11] NCI, MOLEC CARCINOGENESIS LAB, BETHESDA, MD 20892 USA
[12] UNIV MICHIGAN, DEPT BIOL CHEM, ANN ARBOR, MI 48109 USA
[13] UNIV ILLINOIS, DEPT BIOCHEM, URBANA, IL 61801 USA
[14] SAITAMA CANC CTR, INA, SAITAMA 362, JAPAN
[15] HIROSHIMA UNIV, SCH DENT,DEPT BIOCHEM, HIROSHIMA 734, JAPAN
关键词
D O I
10.1089/dna.1993.12.1
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
We provide here a list of 221 P450 genes and 12 putative pseudogenes that have been characterized as of December 14, 1992. These genes have been described in 31 eukaryotes (including 11 mammalian and 3 plant species) and 11 prokaryotes. Of 36 gene families so far described, 12 families exist in all mammals examined to date. These 12 families comprise 22 mammalian subfamilies, of which 17 and 15 have been mapped in the human and mouse genome, respectively. To date, each subfamily appears to represent a cluster of tightly linked genes. This revision supersedes the previous updates [Nebert et al., DNA 6, 1-11, 1987; Nebert et al., DNA 8, 1-13, 1989; Nebert et al., DNA Cell Biol. 10, 1-14 (1991)] in which a nomenclature system, based on divergent evolution of the superfamily, has been described. For the gene and cDNA, we recommend that the italicized root symbol ''CYP'' for human (''Cyp'' for mouse), representing ''cytochrome P450,'' be followed by an Arabic number denoting the family, a letter designating the subfamily (when two or more exist), and an Arabic numeral representing the individual gene within the subfamily. A hyphen should precede the final number in mouse genes. ''P'' (''p'' in mouse) after the gene number denotes a pseudogene. If a gene is the sole member of a family, the subfamily letter and gene number need not be included. We suggest that the human nomenclature system be used for all species other than mouse. The mRNA and enzyme in all species (including mouse) should include all capital letters, without italics or hyphens. This nomenclature system is identical to that proposed in our 1991 update. Also included in this update is a listing of available data base accession numbers for P450 DNA and protein sequences. We also discuss the likelihood that this ancient gene superfamily has existed for more than 3.5 billion years, and that the rate of P450 gene evolution appears to be quite nonlinear. Finally, we describe P450 genes that have been detected by expressed sequence tags (ESTs), as well as the relationship between the P450 and the nitric oxide synthase gene superfamilies, as a likely example of convergent evolution.
引用
收藏
页码:1 / 51
页数:51
相关论文
共 613 条
  • [1] SELECTIVE CHEMICAL MODIFICATION OF CYTOCHROME-P-450SCC LYSINE RESIDUES - IDENTIFICATION OF LYSINES INVOLVED IN THE INTERACTION WITH ADRENODOXIN
    ADAMOVICH, TB
    PIKULEVA, IA
    CHASHCHIN, VL
    USANOV, SA
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 996 (03) : 247 - 253
  • [2] SEQUENCE IDENTIFICATION OF 2,375 HUMAN BRAIN GENES
    ADAMS, MD
    DUBNICK, M
    KERLAVAGE, AR
    MORENO, R
    KELLEY, JM
    UTTERBACK, TR
    NAGLE, JW
    FIELDS, C
    VENTER, JC
    [J]. NATURE, 1992, 355 (6361) : 632 - 634
  • [3] SEGMENTAL HOMOLOGIES IN THE CODING AND 3' NON-CODING SEQUENCES OF RAT-LIVER CYTOCHROME-P-450E AND CYTOCHROME-P450B CDNAS AND CYTOCHROME-P-450E-LIKE GENES
    AFFOLTER, M
    ANDERSON, A
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 118 (02) : 655 - 662
  • [4] CDNA CLONES FOR LIVER CYTOCHROME-P-450S FROM INDIVIDUAL AROCLOR-TREATED RATS - CONSTITUTIVE EXPRESSION OF A NEW P-450 GENE RELATED TO PHENOBARBITAL-INDUCIBLE FORMS
    AFFOLTER, M
    LABBE, D
    JEAN, A
    RAYMOND, M
    NOEL, D
    LABELLE, Y
    PARENTVAUGEOIS, C
    LAMBERT, M
    BOJANOWSKI, R
    ANDERSON, A
    [J]. DNA-A JOURNAL OF MOLECULAR & CELLULAR BIOLOGY, 1986, 5 (03): : 209 - 218
  • [5] AHLGREN R, 1990, J BIOL CHEM, V265, P3313
  • [6] VARIATIONS AND CODING FEATURES OF THE SEQUENCE SPANNING THE REPLICATION TERMINUS OF BACILLUS-SUBTILIS 168 AND W23-CHROMOSOMES
    AHN, KS
    WAKE, RG
    [J]. GENE, 1991, 98 (01) : 107 - 112
  • [7] LIVER MESSENGER-RNA PROBES DISCLOSE 2 CYTOCHROME-P-450 GENES DUPLICATED IN TANDEM WITH THE COMPLEMENT C-4 LOCI OF THE MOUSE H-2S REGION
    AMOR, M
    TOSI, M
    DUPONCHEL, C
    STEINMETZ, M
    MEO, T
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (13) : 4453 - 4457
  • [8] MUTATION IN THE CYP21B GENE (ILE-172-]ASN) CAUSES STEROID 21-HYDROXYLASE DEFICIENCY
    AMOR, M
    PARKER, KL
    GLOBERMAN, H
    NEW, MI
    WHITE, PC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (05) : 1600 - 1604
  • [9] CHARACTERIZATION OF SACCHAROPOLYSPORA-ERYTHRAEA CYTOCHROME-P-450 GENES AND ENZYMES, INCLUDING 6-DEOXYERYTHRONOLIDE-B HYDROXYLASE
    ANDERSEN, JF
    HUTCHINSON, CR
    [J]. JOURNAL OF BACTERIOLOGY, 1992, 174 (03) : 725 - 735
  • [10] ANDERSSON S, 1989, J BIOL CHEM, V264, P8222