Activation-Induced Cytidine Deaminase Alters the Subcellular Localization of Tet Family Proteins

被引:33
作者
Arioka, Yuko [1 ,2 ,3 ]
Watanabe, Akira [1 ,4 ]
Saito, Kuniaki [2 ,3 ]
Yamada, Yasuhiro [1 ,4 ]
机构
[1] Kyoto Univ, Dept Reprogramming Sci, Ctr iPS Cell Res & Applicat CiRA, Kyoto, Japan
[2] Kyoto Univ, Grad Sch Med, Kyoto, Japan
[3] Kyoto Univ, Fac Med, Kyoto, Japan
[4] Kyoto Univ, Inst Integrated Cell Mat Sci WPI iCeMS, Kyoto, Japan
关键词
ACTIVE DNA DEMETHYLATION; SOMATIC HYPERMUTATION; NUCLEAR-EXPORT; AID; 5-METHYLCYTOSINE; 5-HYDROXYMETHYLCYTOSINE; MOUSE; METHYLTRANSFERASES; GLYCOSYLASE; METHYLATION;
D O I
10.1371/journal.pone.0045031
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
Activation-induced cytidine deminase (Aid), a unique enzyme that deaminates cytosine in DNA, shuttles between the nucleus and the cytoplasm. A recent study proposed a novel function of Aid in active DNA demethylation via deamination of 5-hydroxymethylcytosine, which is converted from 5-methylcytosine by the Ten-eleven translocation (Tet) family of enzymes. In this study, we examined the effect of simultaneous expression of Aid and Tet family proteins on the subcellular localization of each protein. We found that overexpressed Aid is mainly localized in the cytoplasm, whereas Tet1 and Tet2 are localized in the nucleus, and Tet3 is localized in both the cytoplasm and the nucleus. However, nuclear Tet proteins were gradually translocated to the cytoplasm when co-expressed with Aid. We also show that Aid-mediated translocation of Tet proteins is associated with Aid shuttling. Here we propose a possible role for Aid as a regulator of the subcellular localization of Tet family proteins.
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页数:9
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共 38 条
[1]   DNA Demethylation Dynamics [J].
Bhutani, Nidhi ;
Burns, David M. ;
Blau, Helen M. .
CELL, 2011, 146 (06) :866-872
[2]   Reprogramming towards pluripotency requires AID-dependent DNA demethylation [J].
Bhutani, Nidhi ;
Brady, Jennifer J. ;
Damian, Mara ;
Sacco, Alessandra ;
Corbel, Stephane Y. ;
Blau, Helen M. .
NATURE, 2010, 463 (7284) :1042-U57
[3]   DNA methylation patterns and epigenetic memory [J].
Bird, A .
GENES & DEVELOPMENT, 2002, 16 (01) :6-21
[4]   OPINION Proteomic identification of multitasking proteins in unexpected locations complicates drug targeting [J].
Butler, Georgina S. ;
Overall, Christopher M. .
NATURE REVIEWS DRUG DISCOVERY, 2009, 8 (12) :935-948
[5]  
Chen TP, 2004, CURR TOP DEV BIOL, V60, P55
[6]   The apolipoprotein B mRNA editing complex performs a multifunctional cycle and suppresses nonsense-mediated decay [J].
Chester, A ;
Somasekaram, A ;
Tzimina, M ;
Jarmuz, A ;
Gisbourne, J ;
O'Keefe, R ;
Scott, J ;
Navaratnam, N .
EMBO JOURNAL, 2003, 22 (15) :3971-3982
[7]   Interaction between anti body-diversification enzyme AID and spliceosome-associated factor CTNNBL1 [J].
Conticello, Silvestro G. ;
Ganesh, Karuna ;
Xue, Kanmin ;
Lu, Mason ;
Rada, Cristina ;
Neuberger, Michael S. .
MOLECULAR CELL, 2008, 31 (04) :474-484
[8]   The AID/APOBEC family of nucleic acid mutators [J].
Conticello, Silvestro G. .
GENOME BIOLOGY, 2008, 9 (06)
[9]   Thymine DNA Glycosylase Is Essential for Active DNA Demethylation by Linked Deamination-Base Excision Repair [J].
Cortellino, Salvatore ;
Xu, Jinfei ;
Sannai, Mara ;
Moore, Robert ;
Caretti, Elena ;
Cigliano, Antonio ;
Le Coz, Madeleine ;
Devarajan, Karthik ;
Wessels, Andy ;
Soprano, Dianne ;
Abramowitz, Lara K. ;
Bartolomei, Marisa S. ;
Rambow, Florian ;
Bassi, Maria Rosaria ;
Bruno, Tiziana ;
Fanciulli, Maurizio ;
Renner, Catherine ;
Klein-Szanto, Andres J. ;
Matsumoto, Yoshihiro ;
Kobi, Dominique ;
Davidson, Irwin ;
Alberti, Christophe ;
Larue, Lionel ;
Bellacosa, Alfonso .
CELL, 2011, 146 (01) :67-79
[10]   Molecular mechanisms of antibody somatic hypermutation [J].
Di Nola, Javier M. ;
Neuberger, Michael S. .
ANNUAL REVIEW OF BIOCHEMISTRY, 2007, 76 :1-22