Identification of the human cytochrome P450, P450RAI-2, which is predominantly expressed in the adult cerebellum and is responsible for all-trans-retinoic acid metabolism

被引:189
作者
White, JA
Ramshaw, H
Taimi, M
Stangle, W
Zhang, AQ
Everingham, S
Creighton, S
Tam, SP
Jones, G
Petkovich, M
机构
[1] Queens Univ, Canc Res Labs, Dept Biochem, Kingston, ON K7L 3N6, Canada
[2] Queens Univ, Dept Med, Kingston, ON K7L 3N6, Canada
[3] Queens Univ, Dept Pathol, Kingston, ON K7L 3N6, Canada
[4] Cytochroma Inc, Kingston, ON K7L 3N6, Canada
关键词
D O I
10.1073/pnas.120161397
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
Retinoids, particularly all-trans-retinoic acid (RA). are potent regulators of cell differentiation, cell proliferation, and apoptosis, The role of all-trans-RA during development and in the maintenance of adult tissues has been well established. The control of all-trans-RA levels in cells and tissues is regulated by the balance between its biosynthesis and its catabolism to inactive metabolites. The cytochrome P450 enzyme P450RAI (herein renamed P450RAI-1) is partially responsible for this inactivation of all-trans-RA. In this report. we describe the identification, molecular cloning. and characterization of a second related enzyme, P450RAI-2, which is also involved in the specific inactivation of all-trans-RA, Transiently transfected P45DRAI-2 can convert all-trans-RA to more polar metabolites including 4-oxo-, 4-OH-, and 18-OH-all-trans-RA. Competition experiments with other retinoids suggest that all-trans-RA is the preferred substrate. The high level of expression of P450RAI-2, particularly in the cerebellum and pens of human adult brain, suggests a unique role for this enzyme in the protection of specific tissues from exposure to retinoids.
引用
收藏
页码:6403 / 6408
页数:6
相关论文
共 28 条
[1]   Mouse P450RAI (CYP26) expression and retinoic acid-inducible retinoic acid metabolism in F9 cells are regulated by retinoic acid receptor γ and retinoid X receptor α [J].
Abu-Abed, SS ;
Beckett, BR ;
Chiba, H ;
Chithalen, JV ;
Jones, G ;
Metzger, D ;
Chambon, P ;
Petkovich, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (04) :2409-2415
[2]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[3]  
BOYLAN JF, 1992, J BIOL CHEM, V267, P21486
[4]   A decade of molecular biology of retinoic acid receptors [J].
Chambon, P .
FASEB JOURNAL, 1996, 10 (09) :940-954
[5]   An essential role for retinoid receptors RARβ and RXRγ in long-term potentiation and depression [J].
Chiang, MY ;
Misner, D ;
Kempermann, G ;
Schikorski, T ;
Giguère, V ;
Sucov, HM ;
Gage, FH ;
Stevens, CF ;
Evans, RM .
NEURON, 1998, 21 (06) :1353-1361
[6]   Metabolic inactivation of retinoic acid by a novel P450 differentially expressed in developing mouse embryos [J].
Fujii, H ;
Sato, T ;
Kaneko, S ;
Gotoh, O ;
FujiiKuriyama, Y ;
Osawa, K ;
Kato, S ;
Hamada, H .
EMBO JOURNAL, 1997, 16 (14) :4163-4173
[7]  
Gudas Lorraine J., 1994, P443
[8]   Regionalized metabolic activity establishes boundaries of retinoic acid signalling [J].
Hollemann, T ;
Chen, YL ;
Grunz, H ;
Pieler, T .
EMBO JOURNAL, 1998, 17 (24) :7361-7372
[9]   A molecular basis for retinoic acid-induced axial truncation [J].
Iulianella, A ;
Beckett, B ;
Petkovich, M ;
Lohnes, D .
DEVELOPMENTAL BIOLOGY, 1999, 205 (01) :33-48
[10]   Current understanding of the molecular actions of vitamin D [J].
Jones, G ;
Strugnell, SA ;
DeLuca, HF .
PHYSIOLOGICAL REVIEWS, 1998, 78 (04) :1193-1231