Polycomb repressive complex 2 is necessary for the normal site-specific O-GlcNAc distribution in mouse embryonic stem cells

被引:106
作者
Myers, Samuel A. [1 ]
Panning, Barbara [2 ]
Burlingame, Alma L. [1 ]
机构
[1] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94158 USA
基金
美国国家卫生研究院;
关键词
EED; Host Cell Factor C1; electron transfer dissociation; DISSOCIATION MASS-SPECTROMETRY; PROTEIN-INTERACTION NETWORK; LINKED N-ACETYLGLUCOSAMINE; DEVELOPMENTAL REGULATORS; X-CHROMOSOME; TARGET GENES; TRANSFERASE; GLCNACYLATION; ROLES; PHOSPHORYLATION;
D O I
10.1073/pnas.1019289108
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
The monosaccharide addition of an N-acetylglucosamine to serine and threonine residues of nuclear and cytosolic proteins (O-GlcNAc) is a posttranslational modification emerging as a general regulator of many cellular processes, including signal transduction, cell division, and transcription. The sole mouse O-GlcNAc transferase (OGT) is essential for embryonic development. To understand the role of OGT in mouse development better, we mapped sites of O-GlcNAcylation of nuclear proteins in mouse embryonic stem cells (ESCs). Here, we unambiguously identify over 60 nuclear proteins as O-GlcNAcylated, several of which are crucial for mouse ESC cell maintenance. Furthermore, we extend the connection between OGT and Polycomb group genes from flies to mammals, showing Polycomb repressive complex 2 is necessary to maintain normal levels of OGT and for the correct cellular distribution of O-GlcNAc. Together, these results provide insight into how OGT may regulate transcription in early development, possibly by modifying proteins important to maintain the ESC transcriptional repertoire.
引用
收藏
页码:9490 / 9495
页数:6
相关论文
共 55 条
[1]   Post-translational modification of p53 in tumorigenesis [J].
Bode, AM ;
Dong, ZG .
NATURE REVIEWS CANCER, 2004, 4 (10) :793-805
[2]   Polycomb complexes repress developmental regulators in murine embryonic stem cells [J].
Boyer, LA ;
Plath, K ;
Zeitlinger, J ;
Brambrink, T ;
Medeiros, LA ;
Lee, TI ;
Levine, SS ;
Wernig, M ;
Tajonar, A ;
Ray, MK ;
Bell, GW ;
Otte, AP ;
Vidal, M ;
Gifford, DK ;
Young, RA ;
Jaenisch, R .
NATURE, 2006, 441 (7091) :349-353
[3]   Core transcriptional regulatory circuitry in human embryonic stem cells [J].
Boyer, LA ;
Lee, TI ;
Cole, MF ;
Johnstone, SE ;
Levine, SS ;
Zucker, JR ;
Guenther, MG ;
Kumar, RM ;
Murray, HL ;
Jenner, RG ;
Gifford, DK ;
Melton, DA ;
Jaenisch, R ;
Young, RA .
CELL, 2005, 122 (06) :947-956
[4]   O-linked β-N-acetylglucosamine (O-GlcNAc): Extensive crosstalk with phosphorylation to regulate signaling and transcription in response to nutrients and stress [J].
Butkinaree, Chutikarn ;
Park, Kyoungsook ;
Hart, Gerald W. .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2010, 1800 (02) :96-106
[5]   Identification of protein O-GlcNAcylation sites using electron transfer dissociation mass spectrometry on native peptides [J].
Chalkley, Robert J. ;
Thalhammer, Agnes ;
Schoepfer, Ralf ;
Burlingame, A. L. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (22) :8894-8899
[6]   Structural insights into mechanism and specificity of O-GlcNAc transferase [J].
Clarke, Andrew J. ;
Hurtado-Guerrero, Ramon ;
Pathak, Shalini ;
Schuttelkopf, Alexander W. ;
Borodkin, Vladimir ;
Shepherd, Sharon M. ;
Ibrahim, Adel F. M. ;
van Aalten, Daan M. F. .
EMBO JOURNAL, 2008, 27 (20) :2780-2788
[7]   Analytical Utility of Small Neutral Losses from Reduced Species in Electron Capture Dissociation Studied Using SwedECD Database [J].
Falth, Maria ;
Savitski, Mikhail M. ;
Nielsen, Michael L. ;
Kjeldsen, Frank ;
Andren, Per E. ;
Zubarev, Roman A. .
ANALYTICAL CHEMISTRY, 2008, 80 (21) :8089-8094
[8]   An RNAi screen of chromatin proteins identifies Tip60-p400 as a regulator of embryonic stem cell identity [J].
Fazzio, Thomas G. ;
Huff, Jason T. ;
Panning, Barbara .
CELL, 2008, 134 (01) :162-174
[9]   Distinct roles of Polycomb group gene products in transcriptionally repressed and active domains of Hoxb8 [J].
Fujimura, Yu-ichi ;
Isono, Kyo-ichi ;
Vidal, Miguel ;
Endoh, Mitsuhiro ;
Kajita, Hiroshi ;
Mizutani-Koseki, Yoko ;
Takihara, Yoshihiro ;
van Lohuizen, Maarten ;
Otte, Arie ;
Jenuwein, Thomas ;
Deschamps, Jacqueline ;
Koseki, Haruhiko .
DEVELOPMENT, 2006, 133 (12) :2371-2381
[10]   Essential Role of the Glycosyltransferase Sxc/Ogt in Polycomb Repression [J].
Gambetta, Maria Cristina ;
Oktaba, Katarzyna ;
Mueller, Juerg .
SCIENCE, 2009, 325 (5936) :93-96