Sequence-dependent Nucleosome Positioning

被引:55
作者
Chung, Ho-Ryun [1 ]
Vingron, Martin [1 ]
机构
[1] Max Planck Inst Mol Genet, Dept Computat Mol Biol, D-14195 Berlin, Germany
关键词
nucleosome; sequence-dependent positioning; histone-DNA interaction; GC preference; structural interpretation; SACCHAROMYCES-CEREVISIAE; MICROCOCCAL NUCLEASE; ANGSTROM RESOLUTION; CORE PARTICLE; DNA-SEQUENCES; CHROMATIN; YEAST; GENOME; TRANSCRIPTION; PROMOTERS;
D O I
10.1016/j.jmb.2008.11.049
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
Eukaryotic DNA is organized into a macromolecular structure called chromatin. The basic repeating unit of chromatin is the nucleosome, which consists of two copies of each of the four core histones and DNA. The nucleosomal organization and the positions of nucleosomes have profound effects on all DNA-dependent processes. Understanding the factors that influence nucleosome positioning is therefore of general interest. Among the many determinants of nucleosome positioning, the DNA sequence has been proposed to have a major role. Here, we analyzed more than 860,000 nucleosomal DNA sequences to identify sequence features that guide the formation of nucleosomes in vivo. We found that both a periodic enrichment of AT base pairs and an out-of-phase oscillating enrichment of GC base pairs as well as the overall preference for GC base pairs are determinants of nucleosome positioning. The preference for GC pairs can be related to a lower energetic cost required for deformation of the DNA to wrap around the histones. In line with this idea, we found that only incorporation of both signal components into a sequence model for nucleosome formation results in maximal predictive performance on a genome-wide scale. In this manner, one achieves greater predictive power than published approaches. Our results confirm the hypothesis that the DNA sequence has a major role in nucleosome positioning in vivo. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1411 / 1422
页数:12
相关论文
共 40 条
[1]   Translational and rotational settings of H2A.Z nucleosomes across the Saccharomyces cerevisiae genome [J].
Albert, Istvan ;
Mavrich, Travis N. ;
Tomsho, Lynn P. ;
Qi, Ji ;
Zanton, Sara J. ;
Schuster, Stephan C. ;
Pugh, B. Franklin .
NATURE, 2007, 446 (7135) :572-576
[2]   Dual role of DNA intrinsic curvature and flexibility in determining nucleosome stability [J].
Anselmi, C ;
Bocchinfuso, G ;
De Santis, P ;
Savino, M ;
Scipioni, A .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 286 (05) :1293-1301
[3]   LOCATION OF THE PRIMARY SITES OF MICROCOCCAL NUCLEASE CLEAVAGE ON THE NUCLEOSOME CORE [J].
COCKELL, M ;
RHODES, D ;
KLUG, A .
JOURNAL OF MOLECULAR BIOLOGY, 1983, 170 (02) :423-446
[4]   Solvent mediated interactions in the structure of the nucleosome core particle at 1.9 Å resolution [J].
Davey, CA ;
Sargent, DF ;
Luger, K ;
Maeder, AW ;
Richmond, TJ .
JOURNAL OF MOLECULAR BIOLOGY, 2002, 319 (05) :1097-1113
[5]   DEFINITIONS AND NOMENCLATURE OF NUCLEIC-ACID STRUCTURE PARAMETERS [J].
DICKERSON, RE .
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 1989, 6 (04) :627-634
[6]   HIGH SEQUENCE SPECIFICITY OF MICROCOCCAL NUCLEASE [J].
DINGWALL, C ;
LOMONOSSOFF, GP ;
LASKEY, RA .
NUCLEIC ACIDS RESEARCH, 1981, 9 (12) :2659-2673
[7]   DNA BENDING AND ITS RELATION TO NUCLEOSOME POSITIONING [J].
DREW, HR ;
TRAVERS, AA .
JOURNAL OF MOLECULAR BIOLOGY, 1985, 186 (04) :773-790
[8]   NUCLEOSOME LOSS ACTIVATES CUP1 AND HIS3 PROMOTERS TO FULLY INDUCED LEVELS IN THE YEAST SACCHAROMYCES-CEREVISIAE [J].
DURRIN, LK ;
MANN, RK ;
GRUNSTEIN, M .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (04) :1621-1629
[9]   STRUCTURE OF NUCLEOSOME CORE PARTICLES OF CHROMATIN [J].
FINCH, JT ;
LUTTER, LC ;
RHODES, D ;
BROWN, RS ;
RUSHTON, B ;
LEVITT, M ;
KLUG, A .
NATURE, 1977, 269 (5623) :29-36
[10]   MICROCOCCAL NUCLEASE AS A DNA STRUCTURAL PROBE - ITS RECOGNITION SEQUENCES, THEIR GENOMIC DISTRIBUTION AND CORRELATION WITH DNA-STRUCTURE DETERMINANTS [J].
FLICK, JT ;
EISSENBERG, JC ;
ELGIN, SCR .
JOURNAL OF MOLECULAR BIOLOGY, 1986, 190 (04) :619-633