Chromatin folding and gene expression: new tools to reveal the spatial organization of genes

被引:11
作者
Brown, KE [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Fac Med, Ctr Clin Sci, Chromosome Biol Grp, London W12 0NN, England
关键词
chromatin; enhancer; hypersensitive site; promoter; transcription;
D O I
10.1023/A:1024966424909
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
An important aim in biology is to understand how gene expression is regulated in the context of chromatin. Much progress has been made towards cracking the 'histone code', which describes the composition and organization of chromatin at high resolution. At the lower resolution provided by microscopy, nuclear compartmentalization has been linked to the control of gene expression and silencing. I will review two new techniques able to reveal the three-dimensional organization of individual loci, providing a view of the folding of the chromatin fibre at an intermediate level of resolution. Carter and colleagues and Tolhuis and colleagues have used the new techniques to demonstrate direct physical contact between the locus control region (LCR) and expressed genes in the active murine beta-globin locus. The techniques will allow us to assess the role of locus organization when transcription is directed by distant regulatory elements. The new techniques (and their foreseeable descendants) will permit investigation of many genomic activities involving physical contact between separate regions of any genome. As such, they provide us with a new level of resolution at which to investigate the functional significance of chromatin organization as patterns of gene expression are initiated and modulated during development.
引用
收藏
页码:423 / 433
页数:11
相关论文
共 69 条
[1]   Epigenetic consequences of nucleosome dynamics [J].
Ahmad, K ;
Henikoff, S .
CELL, 2002, 111 (03) :281-284
[2]   Transcriptional accessibility for genes of multiple tissues and hematopoietic lineages is hierarchically controlled during early hematopoiesis [J].
Akashi, K ;
He, X ;
Chen, J ;
Iwasaki, H ;
Niu, C ;
Steenhard, B ;
Zhang, JW ;
Haug, J ;
Li, LH .
BLOOD, 2003, 101 (02) :383-390
[3]   Intergenic transcription and transinduction of the human beta-globin locus [J].
Ashe, HL ;
Monks, J ;
Wijgerde, M ;
Fraser, P ;
Proudfoot, NJ .
GENES & DEVELOPMENT, 1997, 11 (19) :2494-2509
[4]   SELF-ASSOCIATION OF THE DROSOPHILA-ZESTE PROTEIN IS RESPONSIBLE FOR TRANSVECTION EFFECTS [J].
BICKEL, S ;
PIRROTTA, V .
EMBO JOURNAL, 1990, 9 (09) :2959-2967
[5]   Going the distance: A current view of enhancer action [J].
Blackwood, EM ;
Kadonaga, JT .
SCIENCE, 1998, 281 (5373) :60-63
[6]   Association of transcriptionally silent genes with Ikaros complexes at centromeric heterochromatin [J].
Brown, KE ;
Guest, SS ;
Smale, ST ;
Hahm, K ;
Merkenschlager, M ;
Fisher, AG .
CELL, 1997, 91 (06) :845-854
[7]   Looping versus linking: toward a model for long-distance gene activation [J].
Bulger, M ;
Groudine, M .
GENES & DEVELOPMENT, 1999, 13 (19) :2465-2477
[8]   Effects of cis arrangement of chromatin insulators on enhancer-blocking activity [J].
Cai, HN ;
Shen, P .
SCIENCE, 2001, 291 (5503) :493-495
[9]   Long-range chromatin regulatory interactions in vivo [J].
Carter, D ;
Chakalova, L ;
Osborne, CS ;
Dai, YF ;
Fraser, P .
NATURE GENETICS, 2002, 32 (04) :623-626
[10]   Maintenance of stable heterochromatin domains by dynamic HP1 binding [J].
Cheutin, T ;
McNairn, AJ ;
Jenuwein, T ;
Gilbert, DM ;
Singh, PB ;
Misteli, T .
SCIENCE, 2003, 299 (5607) :721-725