Capturing chromosome conformation

被引:2594
作者
Dekker, J [1 ]
Rippe, K
Dekker, M
Kleckner, N
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[2] Deutsch Krebsforschungszentrum, D-69120 Heidelberg, Germany
[3] Univ Heidelberg, Kirchhoff Inst Phys, Phys Mol Biol Prozesse, D-69120 Heidelberg, Germany
关键词
D O I
10.1126/science.1067799
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We describe an approach to detect the frequency of interaction between any two genomic loci. Generation of a matrix of interaction frequencies between sites on the same or different chromosomes reveals their relative spatial disposition and provides information about the physical properties of the chromatin fiber. This methodology can be applied to the spatial organization of entire genomes in organisms from bacteria to human. Using the yeast Saccharomyces cerevisiae, we could confirm known qualitative features of chromosome organization within the nucleus and dynamic changes in that organization during meiosis. We also analyzed yeast chromosome III at the G(1) stage of the cell cycle. We found that chromatin is highly flexible throughout. Furthermore, functionally distinct AT- and GC-rich domains were found to exhibit different conformations, and a population-average 3D model of chromosome III could be determined. Chromosome III emerges as a contorted ring.
引用
收藏
页码:1306 / 1311
页数:6
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