Single-base Resolution Nucleosome Mapping on DNA Sequences

被引:33
|
作者
Gabdank, I. [1 ]
Barash, D. [1 ]
Trifonov, E. N. [2 ,3 ]
机构
[1] Ben Gurion Univ Negev, Dept Comp Sci, IL-84105 Beer Sheva, Israel
[2] Univ Haifa, Genome Divers Ctr, Inst Evolut, IL-31905 Haifa, Israel
[3] Masaryk Univ, Dept Funct Genom & Prote, Inst Expt Biol, Fac Sci, CZ-62500 Brno, Czech Republic
来源
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS | 2010年 / 28卷 / 01期
基金
以色列科学基金会;
关键词
Chromatin code; DNA hendability; Nucleosome DNA; Nucleosome positioning; Nucleosome structure; CORE PARTICLE; PAIR DNA; CHROMATIN; ALIGNMENT; CRYSTALS; POSITION; PATTERN; SITES; PITCH;
D O I
10.1080/07391102.2010.10507347
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
Nucleosome DNA bendahility pattern extracted from large nucleosome DNA database of C. elegans is used for construction of full length (116 dinucleotide positions) nucleosome DNA bendahility matrix. The matrix can he used for sequence-directed mapping of the nucleosomes on the sequences. Several alternative positions for a given nucleosome are typically predicted. separated by multiples of nucleosome DNA period. The corresponding computer program is successfully tested on best known experimental examples of accurately positioned nucleosomes. The uncertainty of the computational mapping is +/- 1 base. The procedure is placed on publicly accessible server and can he applied to any DNA sequence of interest.
引用
收藏
页码:107 / 121
页数:15
相关论文
共 50 条
  • [21] Single-base resolution analysis of DNA epigenome via high-throughput sequencing
    Jinying Peng
    Bo Xia
    Chengqi Yi
    Science China(Life Sciences), 2016, 59 (03) : 219 - 226
  • [22] Selective Chemical Labeling and Sequencing of 5-Hydroxymethylcytosine in DNA at Single-Base Resolution
    Li, Xiaogang
    Shi, Xinxin
    Gong, Yin
    Guo, Wenting
    Liu, Yuanrui
    Peng, Chunwei
    Xu, Yingchun
    FRONTIERS IN GENETICS, 2021, 12
  • [23] Selective Chemical Labeling and Sequencing of 5-Carboxylcytosine in DNA at Single-Base Resolution
    Xie, Yalun
    Wang, Yafen
    He, Zhiyong
    Yang, Wei
    Fu, Boshi
    Zou, Guangrong
    Zhang, Xiong
    Huang, Jinguo
    Zhou, Xiang
    ANALYTICAL CHEMISTRY, 2020, 92 (18) : 12710 - 12715
  • [24] ZIP-seq: genome-wide mapping of trinucleotide repeats at single-base resolution
    Xu, Xingxing
    Tao, Yonghui
    Fu, Xing
    Yu, Tao
    Li, Yuanyuan
    Chen, Kan
    Ding, Xiaoyan
    Ruan, Kangcheng
    Jing, Naihe
    Hu, Ronggui
    JOURNAL OF MOLECULAR CELL BIOLOGY, 2014, 6 (01) : 93 - 96
  • [25] Transcriptome-wide mapping of N3-methylcytidine modification at single-base resolution
    Gao, Yunyi
    Hou, Jingyu
    Wei, Saisai
    Wu, Canlan
    Yan, Sujun
    Sheng, Jia
    Zhang, Jun
    Chen, Zhanghui
    Gao, Xiangwei
    NUCLEIC ACIDS RESEARCH, 2025, 53 (05)
  • [27] Separation of single-base sequential isomers of single-stranded DNA by capillary electrophoresis and its application in the discrimination of single-base DNA mutations
    Sakurai, Takao
    Hoshino, Hitoshi
    Takahashi, Toru
    JOURNAL OF SEPARATION SCIENCE, 2017, 40 (15) : 3153 - 3160
  • [28] Sequencing 5-Hydroxymethyluracil at Single-Base Resolution
    Kawasaki, Fumiko
    Cuesta, Sergio Martinez
    Beraldi, Dario
    Mahtey, Areeb
    Hardisty, Robyn E.
    Carrington, Mark
    Balasubramanian, Shankar
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 57 (31) : 9694 - 9696
  • [29] A deep learning model for characterizing protein-RNA interactions from sequences at single-base resolution
    Shen, Xilin
    Hou, Yayan
    Wang, Xueer
    Zhang, Chunyong
    Liu, Jilei
    Shen, Hongru
    Wang, Wei
    Yang, Yichen
    Yang, Meng
    Yang, Yayan
    Zhang, Jin
    Sun, Yan
    Chen, Kexin
    Shi, Lei
    Li, Xiangchun
    PATTERNS, 2025, 6 (01):
  • [30] MBRidge: an accurate and cost-effective method for profiling DNA methylome at single-base resolution
    Cai, Wanshi
    Mao, Fengbiao
    Teng, Huajing
    Cai, Tao
    Zhao, Fangqing
    Wu, Jinyu
    Sun, Zhong Sheng
    JOURNAL OF MOLECULAR CELL BIOLOGY, 2015, 7 (04) : 299 - 313