Insights into DNA hydroxymethylation in the honeybee from in-depth analyses of TET dioxygenase

被引:56
作者
Wojciechowski, Marek [1 ]
Rafalski, Dominik [1 ]
Kucharski, Robert [2 ]
Misztal, Katarzyna [1 ]
Maleszka, Joanna [2 ]
Bochtler, Matthias [1 ]
Maleszka, Ryszard [2 ]
机构
[1] Int Inst Mol & Cell Biol, Struct Biol Lab, PL-02109 Warsaw, Poland
[2] Australian Natl Univ, Res Sch Biol, Canberra, ACT 0200, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
epigenetic code; epigenomics; brain plasticity; phenotypic polymorphism; demethylation; social insect; 5-HYDROXYMETHYLCYTOSINE; METHYLATION; 5-METHYLCYTOSINE; DEMETHYLATION; PHENOTYPES; MECHANISMS; DYNAMICS; ERASURE; BASE;
D O I
10.1098/rsob.140110
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In mammals, a family of TET enzymes producing oxidized forms of 5-methylcytosine (5mC) plays an important role in modulating DNA demethylation dynamics. In contrast, nothing is known about the function of a single TET orthologue present in invertebrates. Here, we show that the honeybee TET (AmTET) catalytic domain has dioxygenase activity and converts 5mC to 5-hydroxymethylcytosine (5hmC) in a HEK293T cell assay. In vivo, the levels of 5hmC are condition-dependent and relatively low, but in testes and ovaries 5hmC is present at approximately 7-10% of the total level of 5mC, which is comparable to that reported for certain mammalian cells types. AmTET is alternatively spliced and highly expressed throughout development and in adult tissues with the highest expression found in adult brains. Our findings reveal an additional level of flexible genomic modifications in the honeybee that may be important for the selection of multiple pathways controlling contrasting phenotypic outcomes in this species. In a broader context, our study extends the current, mammalian-centred attention to TET-driven DNA hydroxymethylation to an easily manageable organism with attractive and unique biology.
引用
收藏
页数:9
相关论文
共 37 条
[1]   Mechanisms of DNA methylation and demethylation in mammals [J].
Auclair, Ghislain ;
Weber, Michael .
BIOCHIMIE, 2012, 94 (11) :2202-2211
[2]   DNA Demethylation Dynamics [J].
Bhutani, Nidhi ;
Burns, David M. ;
Blau, Helen M. .
CELL, 2011, 146 (06) :866-872
[3]  
Chahwan R, 2011, DISCOV MED, V11, P233
[4]   Epigenetic reprogramming: Enforcer or enabler of developmental fate? [J].
Combes, Alexander N. ;
Whitelaw, Emma .
DEVELOPMENT GROWTH & DIFFERENTIATION, 2010, 52 (06) :483-491
[5]   Extensive histone post-translational modification in honey bees [J].
Dickman, Mark J. ;
Kucharski, Robert ;
Maleszka, Ryszard ;
Hurd, Paul J. .
INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2013, 43 (02) :125-137
[6]   Kin conflict in insect societies: a new epigenetic perspective [J].
Drewell, Robert A. ;
Lo, Nathan ;
Oxley, Peter R. ;
Oldroyd, Benjamin P. .
TRENDS IN ECOLOGY & EVOLUTION, 2012, 27 (07) :367-373
[7]   Epigenetics and the environment: emerging patterns and implications [J].
Feil, Robert ;
Fraga, Mario F. .
NATURE REVIEWS GENETICS, 2012, 13 (02) :97-109
[8]   DNA methylation dynamics, metabolic fluxes, gene splicing, and alternative phenotypes in honey bees [J].
Foret, Sylvain ;
Kucharski, Robert ;
Pellegrini, Matteo ;
Feng, Suhua ;
Jacobsen, Steven E. ;
Robinson, Gene E. ;
Maleszka, Ryszard .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (13) :4968-4973
[9]   Methylation of tRNAAsP by the DNA methyltransferase homolog Dnmt2 [J].
Goll, MG ;
Kirpekar, F ;
Maggert, KA ;
Yoder, JA ;
Hsieh, CL ;
Zhang, XY ;
Golic, KG ;
Jacobsen, SE ;
Bestor, TH .
SCIENCE, 2006, 311 (5759) :395-398
[10]   The role of Tet3 DNA dioxygenase in epigenetic reprogramming by oocytes [J].
Gu, Tian-Peng ;
Guo, Fan ;
Yang, Hui ;
Wu, Hai-Ping ;
Xu, Gui-Fang ;
Liu, Wei ;
Xie, Zhi-Guo ;
Shi, Linyu ;
He, Xinyi ;
Jin, Seung-gi ;
Iqbal, Khursheed ;
Shi, Yujiang Geno ;
Deng, Zixin ;
Szabo, Piroska E. ;
Pfeifer, Gerd P. ;
Li, Jinsong ;
Xu, Guo-Liang .
NATURE, 2011, 477 (7366) :606-U136