Cloning and sequencing of cytochrome P450 1A complementary DNA in eel (Anguilla japonica)

Citation
R. Mitsuo et al., Cloning and sequencing of cytochrome P450 1A complementary DNA in eel (Anguilla japonica), MAR BIOTEC, 1(4), 1999, pp. 353-358
Citations number
22
Categorie Soggetti
Aquatic Sciences
Journal title
MARINE BIOTECHNOLOGY
ISSN journal
14362228 → ACNP
Volume
1
Issue
4
Year of publication
1999
Pages
353 - 358
Database
ISI
SICI code
1436-2228(199907/08)1:4<353:CASOCP>2.0.ZU;2-Y
Abstract
Cytochrome P450 1A (CYP1A) complementary DNA was isolated from eel (Anguill a japonica) liver treated with 3-methylcholanthrene. The cDNA contained a 5 ' untranslated region of 163 bp, an open reading flame of 1560 bp coding fo r 519 amino acids and a stop codon, and a 3' untranslated region of 1730 bp . The predicted molecular weight was approximately 58.4 kDa. The deduced am ino acid sequence exhibited identities with reported CYP1A sequences of 80% for rainbow trout, 79% for scup, 76% for plaice and butterfly fish, and 74 % for toadfish. When compared with mammalian CYP proteins, the eel CYP1A wa s more similar to CYP1A1 (54%-56%) than to CYP1A2 (49%-52%). Northern and S outhern blot analyses showed two distinct bands, suggesting the existence o f another 3-methylcholanthrene-inducible CYP1A gene in eel.