Ornithine Aminotransferase, an Important Glutamate-Metabolizing Enzyme at the Crossroads of Multiple Metabolic Pathways

被引:97
作者
Ginguay, Antonin [1 ,2 ]
Cynober, Luc [1 ,2 ]
Curis, Emmanuel [3 ,4 ,5 ,6 ]
Nicolis, Ioannis [3 ,7 ]
机构
[1] Cochin Hosp, AP HP, GH HUPC, Clin Chem, F-75014 Paris, France
[2] Univ Paris 05, Fac Pharm, EA 4466 PRETRAM, Lab Biol Nutr, F-75006 Paris, France
[3] Univ Paris 05, Fac Pharm, Lab Biomath, Plateau iB2, F-75006 Paris, France
[4] Univ Paris 05, INSERM, UMR 1144, F-75006 Paris, France
[5] Univ Paris 05, UMR 1144, F-75006 Paris, France
[6] Hop St Louis, AP HP, Serv Biostat & Informat Med, F-75006 Paris, France
[7] Univ Paris 05, Fac Pharm, EA 4064 Epidemiol Environnementale Impact Sanita, F-75006 Paris, France
来源
BIOLOGY-BASEL | 2017年 / 6卷 / 01期
关键词
ornithine aminotransferase; glutamate; ornithine; gyrate atrophy; PROTEIN INTERACTION NETWORK; DELTA-AMINO-TRANSFERASE; GYRATE ATROPHY; RAT-LIVER; KETOACID AMINOTRANSFERASE; SERINE DEHYDRATASE; SMALL-INTESTINE; HEPATOCELLULAR-CARCINOMA; CARBOHYDRATE REPRESSION; SUBSTRATE-SPECIFICITY;
D O I
10.3390/biology6010018
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ornithine -aminotransferase (OAT, E.C. 2.6.1.13) catalyzes the transfer of the -amino group from ornithine (Orn) to -ketoglutarate (aKG), yielding glutamate-5-semialdehyde and glutamate (Glu), and vice versa. In mammals, OAT is a mitochondrial enzyme, mainly located in the liver, intestine, brain, and kidney. In general, OAT serves to form glutamate from ornithine, with the notable exception of the intestine, where citrulline (Cit) or arginine (Arg) are end products. Its main function is to control the production of signaling molecules and mediators, such as Glu itself, Cit, GABA, and aliphatic polyamines. It is also involved in proline (Pro) synthesis. Deficiency in OAT causes gyrate atrophy, a rare but serious inherited disease, a further measure of the importance of this enzyme.
引用
收藏
页数:38
相关论文
共 231 条
[91]   STUDIES ON TURNOVER RATES OF ORNITHINE AMINOTRANSFERASE IN MORRIS HEPATOMA 44 AND HOST LIVER [J].
KOBAYASHI, K ;
MORRIS, HP ;
KATUNUMA, N .
JOURNAL OF BIOCHEMISTRY, 1976, 80 (05) :1085-1089
[92]   MOLECULAR-CLONING AND NUCLEOTIDE-SEQUENCE ANALYSIS OF MESSENGER-RNA FOR HUMAN-KIDNEY ORNITHINE AMINOTRANSFERASE - AN EXAMINATION OF ORNITHINE AMINOTRANSFERASE ISOZYMES BETWEEN LIVER AND KIDNEY [J].
KOBAYASHI, T ;
NISHII, M ;
TAKAGI, Y ;
TITANI, K ;
MATSUZAWA, T .
FEBS LETTERS, 1989, 255 (02) :300-304
[93]   Large-scale identification of c-MYC-associated proteins using a combined TAP/MudPIT approach [J].
Koch, Heike B. ;
Zhang, Ru ;
Verdoodt, Berlinda ;
Bailey, Aaron ;
Zhang, Chang-Dong ;
Yates, John R., III ;
Menssen, Antje ;
Hermeking, Heiko .
CELL CYCLE, 2007, 6 (02) :205-217
[94]   The human neonatal small intestine has the potential for arginine synthesis; developmental changes in the expression of arginine-synthesizing and -catabolizing enzymes [J].
Kohler, Eleonore S. ;
Sankaranarayanan, Selvakumari ;
van Ginneken, Christa J. ;
van Dijk, Paul ;
Vermeulen, Jacqueline L. M. ;
Ruijter, Jan M. ;
Lamers, Wouter H. ;
Bruder, Elisabeth .
BMC DEVELOPMENTAL BIOLOGY, 2008, 8
[95]   STUDIES ON NEW INTRACELLULAR PROTEASES IN VARIOUS ORGANS OF RATS - PARTICIPATION OF PROTEASES IN DEGRADATION OF ORNITHINE AMINOTRANSFERASE INVITRO AND INVIVO [J].
KOMINAMI, E ;
KATUNUMA, N .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1976, 62 (03) :425-430
[96]   COLOCALIZATION IN PERICENTRAL HEPATOCYTES IN ADULT MICE AND SIMILARITY IN DEVELOPMENTAL EXPRESSION PATTERN OF ORNITHINE AMINOTRANSFERASE AND GLUTAMINE-SYNTHETASE MESSENGER-RNA [J].
KUO, FC ;
HWU, WL ;
VALLE, D ;
DARNELL, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (21) :9468-9472
[97]  
Ladeuix B., 2013, THESIS
[98]   Underestimated contribution of skeletal muscle in ornithine metabolism during mouse postnatal development [J].
Ladeuix, Benjamin ;
Duchamp, Claude ;
Levillain, Olivier .
AMINO ACIDS, 2014, 46 (01) :167-176
[99]   ON THE METABOLISM OF ORNITHINE IN SYNAPTOSOMAL PREPARATIONS [J].
LAPINJOKI, SP ;
PAJUNEN, AEI ;
PULKKA, AE ;
PIHA, RS .
NEUROCHEMICAL RESEARCH, 1982, 7 (06) :645-655
[100]   PKCε Promotes Oncogenic Functions of ATF2 in the Nucleus while Blocking Its Apoptotic Function at Mitochondria [J].
Lau, Eric ;
Kluger, Harriet ;
Varsano, Tal ;
Lee, KiYoung ;
Scheffler, Immo ;
Rimm, David L. ;
Ideker, Trey ;
Ronai, Ze'ev A. .
CELL, 2012, 148 (03) :543-555