Gene activation and deactivation related changes in the three-dimensional structure of chromatin

被引:35
作者
Wegel, E
Shaw, P
机构
[1] John Innes Ctr Plant Sci Res, Dept Cell & Dev Biol, Norwich NR4 7UH, Norfolk, England
[2] John Innes Ctr Plant Sci Res, Sainsbury Lane, Norwich NR4 7UH, Norfolk, England
关键词
D O I
10.1007/s00412-005-0015-7
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
Chromatin in the interphase nucleus is dynamic, decondensing where genes are activated and condensing where they are silenced. Local chromatin remodelling to a more open structure during gene activation is followed by changes in nucleosome distribution through the action of the transcriptional machinery. This leads to chromatin expansion and looping out of whole genomic regions. Such chromatin loops can extend beyond the chromosome territory. As several studies point to the location of transcription sites inside chromosome territories as well as at their periphery, extraterritorial loops cannot simply be a mechanism for making transcribed genes accessible to the transcriptional machinery and must occur for other reasons. The level of decondensation within an activated region varies greatly and probably depends on the density of activated genes and the number of engaged RNA polymerases. Genes that are silenced during development form a more closed chromatin structure. Specific histone modifications are correlated with gene activation and silencing, and silenced genes may become associated with heterochromatin protein 1 homologues or with polycomb group complexes. Several levels of chromatin packaging are found in the nucleus relating to the different functions of and performed by active genes; euchromatic and heterochromatic regions and the models explaining higher-order chromatin structure are still disputed.
引用
收藏
页码:331 / 337
页数:7
相关论文
共 71 条
[1]   Transcription sites are not correlated with chromosome territories in wheat nuclei [J].
Abranches, R ;
Beven, AF ;
Aragón-Alcaide, L ;
Shaw, PJ .
JOURNAL OF CELL BIOLOGY, 1998, 143 (01) :5-12
[2]   Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain [J].
Bannister, AJ ;
Zegerman, P ;
Partridge, JF ;
Miska, EA ;
Thomas, JO ;
Allshire, RC ;
Kouzarides, T .
NATURE, 2001, 410 (6824) :120-124
[3]   Nucleosomes, linker DNA, and linker histone form a unique structural motif that directs the higher-order folding and compaction of chromatin [J].
Bednar, J ;
Horowitz, RA ;
Grigoryev, SA ;
Carruthers, LM ;
Hansen, JC ;
Koster, AJ ;
Woodcock, CL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (24) :14173-14178
[4]   VISUALIZATION OF G1 CHROMOSOMES - A FOLDED, TWISTED, SUPERCOILED CHROMONEMA MODEL OF INTERPHASE CHROMATID STRUCTURE [J].
BELMONT, AS ;
BRUCE, K .
JOURNAL OF CELL BIOLOGY, 1994, 127 (02) :287-302
[5]   From DNA structure to gene expression: mediators of nuclear compartmentalization and dynamics [J].
Bode, J ;
Goetze, S ;
Heng, H ;
Krawetz, SA ;
Benham, C .
CHROMOSOME RESEARCH, 2003, 11 (05) :435-445
[6]   Chromatin decondensation and nuclear reorganization of the HoxB locus upon induction of transcription [J].
Chambeyron, S ;
Bickmore, WA .
GENES & DEVELOPMENT, 2004, 18 (10) :1119-1130
[7]   The transcriptional enhancer of the pea plastocyanin gene associates with the nuclear matrix and regulates gene expression through histone acetylation [J].
Chua, YL ;
Watson, LA ;
Gray, JC .
PLANT CELL, 2003, 15 (06) :1468-1479
[8]   Ultrastructural analysis of transcription and splicing in the cell nucleus after bromo-UTP microinjection [J].
Cmarko, D ;
Verschure, PJ ;
Martin, TE ;
Dahmus, ME ;
Krause, S ;
Fu, XD ;
van Driel, R ;
Fakan, S .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (01) :211-223
[9]   Molecular biology - The organization of replication and transcription [J].
Cook, PR .
SCIENCE, 1999, 284 (5421) :1790-1795
[10]   Heterochromatin-many flavours, common themes [J].
Craig, JM .
BIOESSAYS, 2005, 27 (01) :17-28