Interchromosomal interactions: A genomic love story of kissing chromosomes

被引:87
作者
Maass, Philipp G. [1 ,6 ]
Barutcu, A. Rasim [1 ,2 ,7 ]
Rinn, John L. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[2] Broad Inst Massachusetts Inst Technol & Harvard, Cambridge, MA 02142 USA
[3] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[4] Beth Israel Deaconess Med Ctr, Dept Pathol, 330 Brookline Ave, Boston, MA 02215 USA
[5] Univ Colorado, Dept Biochem, BioFrontiers, Boulder, CO 80309 USA
[6] Hosp Sick Children, Genet & Genome Biol Program, Peter Gilgan Ctr Res & Learning, Toronto, ON, Canada
[7] Univ Toronto, Donnelly Ctr, Toronto, ON, Canada
基金
美国国家卫生研究院;
关键词
INTRINSICALLY DISORDERED REGIONS; CONFORMATION CAPTURE; TRANSCRIPTION FACTORIES; SPATIAL-ORGANIZATION; X-INACTIVATION; 3D GENOME; TERRITORY ARRANGEMENTS; NUCLEAR-ORGANIZATION; TOPOLOGICAL DOMAINS; SEQUENCING REVEALS;
D O I
10.1083/jcb.201806052
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Nuclei require a precise three- and four-dimensional organization of DNA to establish cell-specific gene-expression programs. Underscoring the importance of DNA topology, alterations to the nuclear architecture can perturb gene expression and result in disease states. More recently, it has become clear that not only intrachromosomal interactions, but also interchromosomal interactions, a less studied feature of chromosomes, are required for proper physiological gene-expression programs. Here, we review recent studies with emerging insights into where and why cross-chromosomal communication is relevant. Specifically, we discuss how long noncoding RNAs (lncRNAs) and three-dimensional gene positioning are involved in genome organization and how low-throughput (live-cell imaging) and high-throughput (Hi-C and SPR ITE) techniques contribute to understand the fundamental properties of interchromosomal interactions.
引用
收藏
页码:27 / 38
页数:12
相关论文
共 163 条
[41]   Gene Positioning [J].
Ferrai, Carmelo ;
Jesus de Castro, Ines ;
Lavitas, Liron ;
Chotalia, Mita ;
Pombo, Ana .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2010, 2 (06) :a000588
[42]   Recruitment to the nuclear periphery can alter expression of genes in human cells [J].
Finlan, Lee E. ;
Sproul, Duncan ;
Thomson, Inga ;
Boyle, Shelagh ;
Kerr, Elizabeth ;
Perry, Paul ;
Ylstra, Bauke ;
Chubb, Jonathan R. ;
Bickmore, Wendy A. .
PLOS GENETICS, 2008, 4 (03)
[43]   Formation of new chromatin domains determines pathogenicity of genomic duplications [J].
Franke, Martin ;
Ibrahim, Daniel M. ;
Andrey, Guillaume ;
Schwarzer, Wibke ;
Heinrich, Verena ;
Schoepflin, Robert ;
Kraft, Katerina ;
Kempfer, Rieke ;
Jerkovic, Ivana ;
Chan, Wing-Lee ;
Spielmann, Malte ;
Timmermann, Bernd ;
Wittler, Lars ;
Kurth, Ingo ;
Cambiaso, Paola ;
Zuffardi, Orsetta ;
Houge, Gunnar ;
Lambie, Lindsay ;
Brancati, Francesco ;
Pombo, Ana ;
Vingron, Martin ;
Spitz, Francois ;
Mundlos, Stefan .
NATURE, 2016, 538 (7624) :265-+
[44]   An Overview of Genome Organization and How We Got There: from FISH to Hi-C [J].
Fraser, James ;
Williamson, Iain ;
Bickmore, Wendy A. ;
Dostie, Josee .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2015, 79 (03) :347-372
[45]   Cell Type Specific Alterations in Interchromosomal Networks across the Cell Cycle [J].
Fritz, Andrew J. ;
Stojkovic, Branislav ;
Ding, Hu ;
Xu, Jinhui ;
Bhattacharya, Sambit ;
Berezney, Ronald .
PLOS COMPUTATIONAL BIOLOGY, 2014, 10 (10)
[46]   CRISPR-dCas9 and sgRNA scaffolds enable dual-colour live imaging of satellite sequences and repeat-enriched individual loci [J].
Fu, Yi ;
Rocha, Pedro P. ;
Luo, Vincent M. ;
Raviram, Ramya ;
Deng, Yan ;
Mazzoni, Esteban O. ;
Skok, Jane A. .
NATURE COMMUNICATIONS, 2016, 7
[47]   FISHing for captured contacts: towards reconciling FISH and 3C [J].
Fudenberg, Geoffrey ;
Imakaev, Maxim .
NATURE METHODS, 2017, 14 (07) :673-+
[48]   Formation of Chromosomal Domains by Loop Extrusion [J].
Fudenberg, Geoffrey ;
Imakaev, Maxim ;
Lu, Carolyn ;
Goloborodko, Anton ;
Abdennur, Nezar ;
Mirny, Leonid A. .
CELL REPORTS, 2016, 15 (09) :2038-2049
[49]   Identification of physical interactions between genomic regions by enChIP-Seq [J].
Fujita, Toshitsugu ;
Yuno, Miyuki ;
Suzuki, Yutaka ;
Sugano, Sumio ;
Fujii, Hodaka .
GENES TO CELLS, 2017, 22 (06) :506-520
[50]   Efficient sequence-specific isolation of DNA fragments and chromatin by in vitro enChIP technology using recombinant CRISPR ribonucleoproteins [J].
Fujita, Toshitsugu ;
Yuno, Miyuki ;
Fujii, Hodaka .
GENES TO CELLS, 2016, 21 (04) :370-377