Tissue Distribution of 5-Hydroxymethylcytosine and Search for Active Demethylation Intermediates

被引:634
作者
Globisch, Daniel [1 ]
Muenzel, Martin [1 ]
Mueller, Markus [1 ]
Michalakis, Stylianos [2 ]
Wagner, Mirko [1 ]
Koch, Susanne [2 ]
Brueckl, Tobias [1 ]
Biel, Martin [2 ]
Carell, Thomas [1 ]
机构
[1] Univ Munich, Ctr Integrated Prot Sci CiPSM, Dept Chem, Munich, Germany
[2] Univ Munich, Ctr Integrated Prot Sci CiPSM, Dept Pharm, Munich, Germany
来源
PLOS ONE | 2010年 / 5卷 / 12期
关键词
DNA METHYLATION; GLYCOSYLASE ACTIVITY; QUANTIFICATION; 5-METHYLCYTOSINE; CONVERSION; DEAMINATION; METABOLISM; NEURONS; REPAIR; DAMAGE;
D O I
10.1371/journal.pone.0015367
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
5-Hydroxymethylcytosine (hmC) was recently detected as the sixth base in mammalian tissue at so far controversial levels. The function of the modified base is currently unknown, but it is certain that the base is generated from 5-methylcytosine (mC). This fuels the hypothesis that it represents an intermediate of an active demethylation process, which could involve further oxidation of the hydroxymethyl group to a formyl or carboxyl group followed by either deformylation or decarboxylation. Here, we use an ultra-sensitive and accurate isotope based LC-MS method to precisely determine the levels of hmC in various mouse tissues and we searched for 5-formylcytosine (fC), 5-carboxylcytosine (caC), and 5-hydroxymethyluracil (hmU) as putative active demethylation intermediates. Our data suggest that an active oxidative mC demethylation pathway is unlikely to occur. Additionally, we show using HPLC-MS analysis and immunohistochemistry that hmC is present in all tissues and cell types with highest concentrations in neuronal cells of the CNS.
引用
收藏
页数:9
相关论文
共 35 条
  • [1] Definitive identification of mammalian 5-hydroxymethyluracil DNA N-glycosylase activity as SMUG1
    Boorstein, RJ
    Cummings, A
    Marenstein, DR
    Chan, MK
    Ma, YL
    Neubert, TA
    Brown, SM
    Teebor, GW
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (45) : 41991 - 41997
  • [2] Parallel Isotope-Based Quantification of Modified tRNA Nucleosides
    Brueckl, Tobias
    Globisch, Daniel
    Wagner, Mirko
    Mueller, Markus
    Carell, Thomas
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (42) : 7932 - 7934
  • [3] 5-HYDROXYMETHYLCYTOSINE DNA GLYCOSYLASE ACTIVITY IN MAMMALIAN TISSUE
    CANNON, SV
    CUMMINGS, A
    TEEBOR, GW
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 151 (03) : 1173 - 1179
  • [4] Measurement and meaning of oxidatively modified DNA lesions in urine
    Cooke, Marcus S.
    Olinski, Ryszard
    Loft, Steffen
    [J]. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2008, 17 (01) : 3 - 14
  • [5] Dnmt1 and Dnmt3a maintain DNA methylation and regulate synaptic function in adult forebrain neurons
    Feng, Jian
    Zhou, Yu
    Campbell, Susan L.
    Le, Thuc
    Li, En
    Sweatt, J. David
    Silva, Alcino J.
    Fan, Guoping
    [J]. NATURE NEUROSCIENCE, 2010, 13 (04) : 423 - U37
  • [6] Mammalian neural stem cells
    Gage, FH
    [J]. SCIENCE, 2000, 287 (5457) : 1433 - 1438
  • [7] TISSUE-SPECIFIC DIFFERENCES IN DNA METHYLATION IN VARIOUS MAMMALS
    GAMASOSA, MA
    MIDGETT, RM
    SLAGEL, VA
    GITHENS, S
    KUO, KC
    GEHRKE, CW
    EHRLICH, M
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 740 (02) : 212 - 219
  • [8] Genome-Wide Reprogramming in the Mouse Germ Line Entails the Base Excision Repair Pathway
    Hajkova, Petra
    Jeffries, Sean J.
    Lee, Caroline
    Miller, Nigel
    Jackson, Stephen P.
    Surani, M. Azim
    [J]. SCIENCE, 2010, 329 (5987) : 78 - 82
  • [9] Houk KN, 2001, CHEMBIOCHEM, V2, P113, DOI 10.1002/1439-7633(20010202)2:2<113::AID-CBIC113>3.0.CO
  • [10] 2-T