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Periodicity in prokaryotic and eukaryotic genomes identified by power spectrum analysis
Authors:Fukushima Atsushi  Ikemura Toshimichi  Kinouchi Makoto  Oshima Taku  Kudo Yoshihiro  Mori Hirotada  Kanaya Shigehiko
Institution:

a Graduate School of Biological Sciences, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0101, Japan

b Division of Evolutionary Genetics, Department of Population Genetics, National Institute of Genetics, The Graduate University for Advanced Studies, Mishima, Shizuoka 411-8540, Japan

c Division of Genetics, Department of Biological Science, The Graduate University for Advanced Studies, Mishima, Shizuoka 411-8540, Japan

d ACT-JST (Research and Development for Applying Advanced Computational Science and Technology, Japan Science and Technology Corporation), City, Japan

e CREST, JST (Japan Science and Technology), City, Japan

f Department of Bio-System Engineering, Faculty of Engineering, Yamagata University, Yonezawa, Yamagata 992-8510, Japan

g Research and Education Center for Genetic Information, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0101, Japan

h Graduate School of Information Science, Nara Institute of Science and Technology, 8916-5, Takayama, Ikoma, Nara 630-0101, Japan

Abstract:We used a power spectrum method to identify periodic patterns in nucleotide sequence, and characterized nucleotide sequences that confer periodicities to prokaryotic and eukaryotic genomes and genomes. A 10-bp periodicity was prevalent in hyperthermophilic bacteria and archaebacteria, and an 11-bp periodicity was prevalent in eubacteria. The 10-bp periodicity was also prevalent in the eukaryotes such as the worm Caenorhabditis elegans. Additionally, in the worm genome, a 68-bp periodicity in chromosome I, a 59-bp periodicity in chromosome II, and a 94-bp periodicity in chromosome III were found. In human chromosomes 21 and 22, approximately 167- or 84-bp periodicity was detected along the entire length of these chromosomes. Because the 167-bp is identical to the length of DNA that forms two complete helical turns in nucleosome organization, we speculated that the respective sequences may correspond to arrays of a special compact form of nucleosomes clustered in specific regions of the human chromosomes. This periodic element contained a high frequency of TGG. TGG-rich sequences are known to form a specific subset of folded DNA structures, and therefore, the sequences might have potential to form specific higher order structures related to the clustered occurrence of a specific form of the speculated nucleosomes.
Keywords:Nucleotide periodicity  Power spectrum analysis  Tandem repeat  Fourier analysis  Long-range correlation
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