Transcription-dependent spatial arrangements of CFTR and adjacent genes in human cell nuclei

被引:221
作者
Zink, D
Amaral, MD
Englmann, A
Lang, S
Clarke, LA
Rudolph, C
Alt, F
Luther, K
Braz, C
Sadoni, N
Rosenecker, J
Schindelhauer, D
机构
[1] Univ Munich, Dept Biol 2, D-82152 Martinsried, Germany
[2] Univ Lisbon, Fac Sci, Dept Chem & Biochem, P-1749016 Lisbon, Portugal
[3] NIH, Ctr Human Genet, P-1649016 Lisbon, Portugal
[4] Univ Munich, Div Mol Pulm, Dept Pediat, D-80337 Munich, Germany
[5] Tech Univ Munich, Inst Human Genet, D-81675 Munich, Germany
[6] Life Sci Ctr Weihenstephan, D-85354 Freising Weihenstephan, Germany
关键词
CFTR; nuclear architecture; gene positioning; chromatin organization; chromosome territory;
D O I
10.1083/jcb.200404107
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We investigated in different human cell types nuclear positioning and transcriptional regulation of the functionally unrelated genes GASZ, CFTR, and CORTBP2, mapping to adjacent loci on human chromosome 7q31. When inactive, GASZ, CFTR, and CORTBP2 preferentially associated with the nuclear periphery and with perinuclear heterochromatin, whereas in their actively transcribed states the gene loci preferentially associated with euchromatin in the nuclear interior. Adjacent genes associated simultaneously with these distinct chromatin fractions localizing at different nuclear regions, in accordance with their individual transcriptional regulation. Although the nuclear localization of CFTR changed after altering its transcription levels, the transcriptional status of CFTR was not changed by driving this gene into a different nuclear environment. This implied that the transcriptional activity affected the nuclear positioning, and not vice versa. Together, the results show that small chromosomal subregions can display highly flexible nuclear organizations that are regulated at the level of individual genes in a transcription-dependent manner.
引用
收藏
页码:815 / 825
页数:11
相关论文
共 38 条
[1]  
Amaral Margarida D, 2004, J Cyst Fibros, V3 Suppl 2, P17, DOI 10.1016/j.jcf.2004.05.047
[2]   Regulated recruitment of HP1 to a euchromatic gene induces mitotically heritable, epigenetic gene silencing: a mammalian cell culture model of gene variegation [J].
Ayyanathan, K ;
Lechner, MS ;
Bell, P ;
Maul, GG ;
Schultz, DC ;
Yamada, Y ;
Tanaka, K ;
Torigoe, K ;
Rauscher, FJ .
GENES & DEVELOPMENT, 2003, 17 (15) :1855-1869
[3]   LARGE-SCALE CHROMATIN STRUCTURAL DOMAINS WITHIN MITOTIC AND INTERPHASE CHROMOSOMES INVIVO AND INVITRO [J].
BELMONT, AS ;
BRAUNFELD, MB ;
SEDAT, JW ;
AGARD, DA .
CHROMOSOMA, 1989, 98 (02) :129-143
[4]   The spatial organization of human chromosomes within the nuclei of normal and emerin-mutant cells [J].
Boyle, S ;
Gilchrist, S ;
Bridger, JM ;
Mahy, NL ;
Ellis, JA ;
Bickmore, WA .
HUMAN MOLECULAR GENETICS, 2001, 10 (03) :211-219
[5]   Dynamic repositioning of genes in the nucleus of lymphocytes preparing for cell division [J].
Brown, KE ;
Baxter, J ;
Graf, D ;
Merkenschlager, M ;
Fisher, AG .
MOLECULAR CELL, 1999, 3 (02) :207-217
[6]   Expression of α- and β-globin genes occurs within different nuclear domains in haemopoietic cells [J].
Brown, KE ;
Amoils, S ;
Horn, JM ;
Buckle, VJ ;
Higgs, DR ;
Merkenschlager, M ;
Fisher, AG .
NATURE CELL BIOLOGY, 2001, 3 (06) :602-606
[7]   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
[8]   Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31 [J].
Cheung, J ;
Petek, E ;
Nakabayashi, K ;
Tsui, LC ;
Vincent, JB ;
Scherer, SW .
GENOMICS, 2001, 78 (1-2) :7-11
[9]   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
[10]   Chromosome territories, nuclear architecture and gene regulation in mammalian cells [J].
Cremer, T ;
Cremer, C .
NATURE REVIEWS GENETICS, 2001, 2 (04) :292-301