Polycomb Proteins Remain Bound to Chromatin and DNA during DNA Replication In Vitro

被引:132
作者
Francis, Nicole J. [1 ]
Follmer, Nicole E. [1 ]
Simon, Matthew D. [2 ,3 ]
Aghia, George [1 ]
Butler, Jeffrey D. [1 ]
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[2] Massachusetts Gen Hosp, Dept Mol Biol, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
GENOME-WIDE ANALYSIS; SIMIAN VIRUS-40 DNA; EARLY MOUSE EMBRYOS; HISTONE H3; TRANSCRIBING POLYMERASE; DROSOPHILA-MELANOGASTER; POLYTENE CHROMOSOMES; H2A UBIQUITYLATION; REPRESSIVE COMPLEX; CELLS;
D O I
10.1016/j.cell.2009.02.017
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
The transcriptional status of a gene can be maintained through multiple rounds of cell division during development. This epigenetic effect is believed to reflect heritable changes in chromatin folding and histone modifications or variants at target genes, but little is known about how these chromatin features are inherited through cell division. A particular challenge for maintaining transcription states is DNA replication, which disrupts or dilutes chromatin-associated proteins and histone modifications. PRC1-class Polycomb group protein complexes are essential for development and are thought to heritably silence transcription by altering chromatin folding and histone modifications. It is not known whether these complexes and their effects are maintained during DNA replication or subsequently re-established. We find that when PRC1-class Polycomb complex-bound chromatin or DNA is replicated in vitro, Polycomb complexes remain bound to replicated templates. Retention of Polycomb proteins through DNA replication may contribute to maintenance of transcriptional silencing through cell division.
引用
收藏
页码:110 / 122
页数:13
相关论文
共 71 条
[21]   From genetics to epigenetics:: the tale of Polycomb group and trithorax group genes [J].
Grimaud, Charlotte ;
Negre, Nicolas ;
Cavalli, Giacomo .
CHROMOSOME RESEARCH, 2006, 14 (04) :363-375
[22]   Chromatin challenges during DNA replication and repair [J].
Groth, Anja ;
Rocha, Walter ;
Verreault, Alain ;
Almouzni, Genevieve .
CELL, 2007, 128 (04) :721-733
[23]   A model for transmission of the H3K27me3 epigenetic mark [J].
Hansen, Klaus H. ;
Bracken, Adrian P. ;
Pasini, Diego ;
Dietrich, Nikolaj ;
Gehani, Simmi S. ;
Monrad, Astrid ;
Rappsilber, Juri ;
Lerdrup, Mads ;
Helin, Kristian .
NATURE CELL BIOLOGY, 2008, 10 (11) :1291-U89
[24]  
JACKMAN J, 2003, METHODS SYNCHRONIZIN
[25]   Genome-wide analysis reveals MOF as a key regulator of dosage compensation and gene expression in Drosophila [J].
Kind, Jop ;
Vaquerizas, Juan M. ;
Gebhardt, Philipp ;
Gentzel, Marc ;
Luscombe, Nicholas M. ;
Bertone, Paul ;
Akhtar, Asifa .
CELL, 2008, 133 (05) :813-828
[26]   Analysis of a polycomb group protein defines regions that link repressive activity on nucleosomal templates to in vivo function [J].
King, IFG ;
Emmons, RB ;
Francis, NJ ;
Wild, B ;
Müller, J ;
Kingston, RE ;
Wu, CT .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (15) :6578-6591
[27]   Native and recombinant polycomb group complexes establish a selective block to template accessibility to repress transcription in vitro [J].
King, IFG ;
Francis, NJ ;
Kingston, RE .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (22) :7919-7928
[28]   A Polycomb group protein complex with sequence-specific DNA-binding and selective methyl-lysine-binding activities [J].
Klymenko, T ;
Papp, B ;
Fischle, W ;
Köcher, T ;
Schelder, M ;
Fritsch, C ;
Wild, B ;
Wilm, M ;
Müller, J .
GENES & DEVELOPMENT, 2006, 20 (09) :1110-1122
[29]   Chromatin challenges during DNA replication: A systems representation [J].
Kohn, Kurt W. ;
Aladjem, Mirit I. ;
Weinstein, John N. ;
Pommier, Yves .
MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (01) :1-7
[30]   Stability and Dynamics of Polycomb Target Sites in Drosophila Development [J].
Kwong, Camilla ;
Adryan, Boris ;
Bell, Ian ;
Meadows, Lisa ;
Russell, Steven ;
Manak, J. Robert ;
White, Robert .
PLOS GENETICS, 2008, 4 (09)