Uncovering the forces between nucleosomes using DNA origami

被引:163
作者
Funke, Jonas J. [1 ,2 ]
Ketterer, Philip [1 ,2 ]
Lieleg, Corinna [3 ]
Schunter, Sarah [3 ]
Korber, Philipp [3 ]
Dietz, Hendrik [1 ,2 ]
机构
[1] Tech Univ Munich, Dept Phys, Coulombwall 4a, Garching, Germany
[2] Tech Univ Munich, Inst Adv Study, Coulombwall 4a, Garching, Germany
[3] Ludwig Maximilians Univ Munchen, Mol Biol, Biomed Ctr, Munich, Germany
来源
SCIENCE ADVANCES | 2016年 / 2卷 / 11期
基金
欧洲研究理事会;
关键词
CHROMATIN FIBER REVEALS; H4 TAIL ACETYLATIONS; CORE PARTICLE; ANGSTROM RESOLUTION; NANOSCALE SHAPES; DOSAGE COMPENSATION; ELECTRON-MICROSCOPY; H4-K16; ACETYLATION; CRYSTAL-STRUCTURE; FOLDING DNA;
D O I
10.1126/sciadv.1600974
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
Revealing the energy landscape for nucleosome association may contribute to the understanding of higher-order chromatin structures and their impact on genome regulation. We accomplish this in a direct measurement by integrating two nucleosomes into a DNA origami-based force spectrometer, which enabled subnanometer-resolution measurements of nucleosome-nucleosome distance frequencies via single-particle electron microscopy imaging. From the data, we derived the Boltzmann-weighted distance-dependent energy landscape for nucleosome pair interactions. We find a shallow but long-range (similar to 6 nm) attractive nucleosome pair potential with a minimum of -1.6 kcal/mol close to direct contact distances. The relative nucleosome orientation had little influence, but histone H4 acetylation or removal of histone tails drastically decreased the interaction strength. Because of the weak and shallow pair potential, high-erorder nucleosome assemblies will be compliant and experience dynamic shape fluctuations in the absence of additional cofactors. Our results contribute to a more accurate description of chromatin and our force spectrometer provides a powerful tool for the direct and high-resolution study of molecular interactions using imaging techniques.
引用
收藏
页数:9
相关论文
共 65 条
[1]   Activation of transcription through histone H4 acetylation by MOF, an acetyltransferase essential for dosage compensation in Drosophila [J].
Akhtar, A ;
Becker, PB .
MOLECULAR CELL, 2000, 5 (02) :367-375
[2]   The effects of histone H4 tail acetylations on cation-induced chromatin folding and self-association [J].
Allahverdi, Abdollah ;
Yang, Renliang ;
Korolev, Nikolay ;
Fan, Yanping ;
Davey, Curt A. ;
Liu, Chuan-Fa ;
Nordenskioeld, Lars .
NUCLEIC ACIDS RESEARCH, 2011, 39 (05) :1680-1691
[3]   Determinants and dynamics of genome accessibility [J].
Bell, Oliver ;
Tiwari, Vijay K. ;
Thomae, Nicolas H. ;
Schuebeler, Dirk .
NATURE REVIEWS GENETICS, 2011, 12 (08) :554-564
[4]   Structure and phase diagram of nucleosome core particles aggregated by multivalent cations [J].
Bertin, Aurelie ;
Mangenot, Stephanie ;
Renouard, Magdalena ;
Durand, Dominique ;
Livolant, Francoise .
BIOPHYSICAL JOURNAL, 2007, 93 (10) :3652-3663
[5]   A combination of different mass spectroscopic techniques for the analysis of dynamic changes of histone modifications [J].
Bonaldi, T ;
Imhof, A ;
Regula, JT .
PROTEOMICS, 2004, 4 (05) :1382-1396
[6]   Structural transitions and elasticity from torque measurements on DNA [J].
Bryant, Z ;
Stone, MD ;
Gore, J ;
Smith, SB ;
Cozzarelli, NR ;
Bustamante, C .
NATURE, 2003, 424 (6946) :338-341
[7]   A primer to scaffolded DNA origami [J].
Castro, Carlos Ernesto ;
Kilchherr, Fabian ;
Kim, Do-Nyun ;
Shiao, Enrique Lin ;
Wauer, Tobias ;
Wortmann, Philipp ;
Bathe, Mark ;
Dietz, Hendrik .
NATURE METHODS, 2011, 8 (03) :221-229
[8]   Characterization of Nucleosome Unwrapping within Chromatin Fibers Using Magnetic Tweezers [J].
Chien, Fan-Tso ;
van der Heijden, Thijn .
BIOPHYSICAL JOURNAL, 2014, 107 (02) :373-383
[9]   The mechanics behind DNA sequence-dependent properties of the nucleosome [J].
Chua, Eugene Y. D. ;
Vasudevan, Dileep ;
Davey, Gabriela E. ;
Wu, Bin ;
Davey, Curt A. .
NUCLEIC ACIDS RESEARCH, 2012, 40 (13) :6338-6352
[10]   Structure of the Drosophila nucleosome core particle highlights evolutionary constraints on the H2A-H2B histone dimer [J].
Clapier, Cedric R. ;
Chakravarthy, Srinivas ;
Petosa, Carlo ;
Fernandez-Tornero, Carlos ;
Luger, Karolin ;
Mueller, Christoph W. .
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2008, 71 (01) :1-7