Cbr1

Summary

Gene Symbol: Cbr1
Description: carbonyl reductase 1
Alias: AW261796, Cbr, carbonyl reductase [NADPH] 1, 15-hydroxyprostaglandin dehydrogenase, Carbonyl reductase [NADPH] 1 (NADPH-dependent carbonyl reductase 1), NADPH-dependent carbonyl reductase 1, prostaglandin 9-ketoreductase, prostaglandin-E(2) 9-reductase
Species: mouse

Top Publications

  1. doi Carbonyl reductase 1 is an essential regulator of skeletal muscle differentiation and regeneration
    Sangbin Lim
    Department of Biochemistry and Molecular Biology, School of Medicine, Kyung Hee University, Seoul 130 701, Republic of Korea
    Int J Biochem Cell Biol 45:1784-93. 2013
  2. ncbi Localization of four human chromosome 21 genes--SOD1, ETS2, IFNAR, and CBR--to two different chromosomes in the marsupial species Macropus eugenii
    S Brookes
    Molecular Embryology and Birth Defects Laboratory, Monash University, Clayton, Victoria, Australia
    Cytogenet Cell Genet 61:25-8. 1992
  3. ncbi High-resolution mapping of D16led-1, Gart, Gas-4, Cbr, Pcp-4, and Erg on distal mouse chromosome 16
    A E Mjaatvedt
    Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205
    Genomics 17:382-6. 1993
  4. ncbi Cloning a cDNA for carbonyl reductase (Cbr) from mouse cerebellum: murine genes that express cbr map to chromosomes 16 and 11
    J Wei
    Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana, 46202, USA
    Genomics 34:147-8. 1996
  5. ncbi Assessment of a mutation in the H5 domain of Girk2 as a candidate for the weaver mutation
    A E Mjaatvedt
    Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
    Genome Res 5:453-63. 1995
  6. ncbi Involvement of two basic residues (Lys-17 and Arg-39) of mouse lung carbonyl reductase in NADP(H)-binding and fatty acid activation: site-directed mutagenesis and kinetic analyses
    M Nakanishi
    Department of Applied Chemistry, Faculty of Engineering, Gifu University
    J Biochem 120:257-63. 1996
  7. ncbi The murine Dyrk protein maps to chromosome 16, localizes to the nucleus, and can form multimers
    W J Song
    Howard Hughes Medical Institute, University of Michigan Medical Center, Ann Arbor 48109, USA
    Biochem Biophys Res Commun 231:640-4. 1997
  8. pmc Physical and comparative mapping of distal mouse chromosome 16. 5 p5
    D E Cabin
    Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205 USA
    Genome Res 8:940-50. 1998
  9. ncbi Cloning and bacterial expression of monomeric short-chain dehydrogenase/reductase (carbonyl reductase) from CHO-K1 cells
    T Terada
    Laboratory of Biochemistry and Molecular Biology, Graduate School of Pharmaceutical Sciences, Osaka University, Japan
    Eur J Biochem 267:6849-57. 2000
  10. ncbi On the cause of mental retardation in Down syndrome: extrapolation from full and segmental trisomy 16 mouse models
    Z Galdzicki
    Section on Brain Physiology and Metabolism, National Institute on Aging, National Institutes of Health, Bethesda, MD 20892, USA
    Brain Res Brain Res Rev 35:115-45. 2001

Scientific Experts

  • Z Galdzicki
  • Sangbin Lim
  • Sung Soo Kim
  • Tae Gyu Choi
  • Joohun Ha
  • M A Rashid
  • Zohra Seregaza
  • R H Reeves
  • L E Olson
  • A E Mjaatvedt
  • Jae Hoon Park
  • Young Gyu Eun
  • Ara Jo
  • Ju Young Shin
  • Kyung Sik Yoon
  • Minh Nam Nguyen
  • Jinhwan Kim
  • K R Jyothi
  • D E Cabin
  • Seonmin Lee
  • Eunyoung Tak
  • Jang H Youn
  • T Terada
  • Jae Bum Kim
  • Jisun Lee
  • Joo Won Lee
  • Insug Kang
  • Marc Jamon
  • Pierre L Roubertoux
  • Bernard Soumireu-Mourat
  • J T Richtsmeier
  • J Leszl
  • W J Song
  • M Nakanishi
  • A Hara
  • J Wei
  • K Nakamura
  • Y Sugihara
  • M Maeda
  • N Inazu
  • R Sato
  • J R Korenberg
  • E E Rue
  • Y K Huo
  • T Wiltshire
  • J W McKee-Johnson
  • L E Matesic
  • S H Chung
  • D M Kurnit
  • B Ghetti
  • Y Deyashiki
  • Y Mitsui
  • N Tanaka
  • K Matsuura
  • T Nonaka
  • M Kakumoto
  • M E Hodes
  • S R Dlouhy
  • L J Long
  • S E Cole
  • G E Breitwieser
  • S Brookes
  • M P Citron
  • J A Graves
  • J B de Haan
  • I Kola
  • G L Forrest
  • P Maccarone
  • M Tymms

Detail Information

Publications13

  1. doi Carbonyl reductase 1 is an essential regulator of skeletal muscle differentiation and regeneration
    Sangbin Lim
    Department of Biochemistry and Molecular Biology, School of Medicine, Kyung Hee University, Seoul 130 701, Republic of Korea
    Int J Biochem Cell Biol 45:1784-93. 2013
    ..Carbonyl reductase 1 (CBR1) reduces highly reactive lipid aldehydes and catalyzes a variety of endogenous and xenobiotic carbonyl compounds...
  2. ncbi Localization of four human chromosome 21 genes--SOD1, ETS2, IFNAR, and CBR--to two different chromosomes in the marsupial species Macropus eugenii
    S Brookes
    Molecular Embryology and Birth Defects Laboratory, Monash University, Clayton, Victoria, Australia
    Cytogenet Cell Genet 61:25-8. 1992
    ..SOD1), the protooncogene ETS2, the interferon alpha/beta receptor gene (IFNAR), and the carbonyl reductase gene (CBR)--in the tammar, Macropus eugenii...
  3. ncbi High-resolution mapping of D16led-1, Gart, Gas-4, Cbr, Pcp-4, and Erg on distal mouse chromosome 16
    A E Mjaatvedt
    Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205
    Genomics 17:382-6. 1993
    ..The map order, including previously mapped reference markers, is (cen)-D16H21S16-D16Led-1-App-Sod-1-Gart-Gas-4-Cbr++ +-wv-Pcp-4-Erg-Ets-2. This gene order recapitulates the order of the genes on human chromosome 21 where known...
  4. ncbi Cloning a cDNA for carbonyl reductase (Cbr) from mouse cerebellum: murine genes that express cbr map to chromosomes 16 and 11
    J Wei
    Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana, 46202, USA
    Genomics 34:147-8. 1996
  5. ncbi Assessment of a mutation in the H5 domain of Girk2 as a candidate for the weaver mutation
    A E Mjaatvedt
    Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA
    Genome Res 5:453-63. 1995
    ..This suggests that if the Girk2 mutation is responsible for the wv phenotype, it does not act by altering these electrical properties of developing GCs...
  6. ncbi Involvement of two basic residues (Lys-17 and Arg-39) of mouse lung carbonyl reductase in NADP(H)-binding and fatty acid activation: site-directed mutagenesis and kinetic analyses
    M Nakanishi
    Department of Applied Chemistry, Faculty of Engineering, Gifu University
    J Biochem 120:257-63. 1996
    ....
  7. ncbi The murine Dyrk protein maps to chromosome 16, localizes to the nucleus, and can form multimers
    W J Song
    Howard Hughes Medical Institute, University of Michigan Medical Center, Ann Arbor 48109, USA
    Biochem Biophys Res Commun 231:640-4. 1997
    ....
  8. pmc Physical and comparative mapping of distal mouse chromosome 16. 5 p5
    D E Cabin
    Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205 USA
    Genome Res 8:940-50. 1998
    ..Comparison of this physical map with that of the corresponding region on Chr. 21 shows conservation not only of gene order but of size in the 3 Mb from Cbr1 to Ets2; distal to Ets2, the human map is expanded.
  9. ncbi Cloning and bacterial expression of monomeric short-chain dehydrogenase/reductase (carbonyl reductase) from CHO-K1 cells
    T Terada
    Laboratory of Biochemistry and Molecular Biology, Graduate School of Pharmaceutical Sciences, Osaka University, Japan
    Eur J Biochem 267:6849-57. 2000
    ..RT-PCR of Chinese hamster tissues suggest that CHO-CR is highly expressed in kidney, testis, brain, heart, liver, uterus and ovary. Southern blotting analysis indicated the complexity of the Chinese hamster carbonyl reductase gene...
  10. ncbi On the cause of mental retardation in Down syndrome: extrapolation from full and segmental trisomy 16 mouse models
    Z Galdzicki
    Section on Brain Physiology and Metabolism, National Institute on Aging, National Institutes of Health, Bethesda, MD 20892, USA
    Brain Res Brain Res Rev 35:115-45. 2001
    ..Changes in timing and synaptic interaction between neurons during development can lead to less than optimal functioning of neural circuitry and signaling then and in later life...
  11. pmc A chromosome 21 critical region does not cause specific Down syndrome phenotypes
    L E Olson
    Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA
    Science 306:687-90. 2004
    ..The DSCR genes were not sufficient and were largely not necessary to produce the facial phenotype. These results refute specific predictions of the prevailing hypothesis of gene action in DS...
  12. ncbi Mouse models of cognitive disorders in trisomy 21: a review
    Zohra Seregaza
    Génomique fonctionnelle, Pathologies, Comportements, P3M, UMR 6196, CNRS Université de la Méditerranée, Marseille, France
    Behav Genet 36:387-404. 2006
    ..This review confirms the crucial but not exclusive contribution of the D21S17-ETS2 region encompassing 16 genes to cognitive disorders...
  13. doi Carbonyl reductase 1 protects pancreatic β-cells against oxidative stress-induced apoptosis in glucotoxicity and glucolipotoxicity
    M A Rashid
    Medical Science and Engineering Research Center for Bioreaction to Reactive Oxygen Species and Biomedical Science Institute BK 21, Department of Biochemistry and Molecular Biology, School of Medicine, Kyung Hee University, Seoul 130 701, Korea
    Free Radic Biol Med 49:1522-33. 2010
    Carbonyl reductase 1 (CBR1) plays an important role in the detoxification of reactive lipid aldehydes. Oxidative stress has been implicated in the pathogenesis of pancreatic β-cell failure...