Oligonucleotide sequence motifs as nucleosome positioning signals.

To gain a better understanding of the sequence patterns that characterize positioned nucleosomes, we first performed an analysis of the periodicities of the 256 tetranucleotides in a yeast genome-wide library of nucleosomal DNA sequences that was prepared by in vitro reconstitution. The approach ent...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Clayton K Collings, Alfonso G Fernandez, Chad G Pitschka, Troy B Hawkins, John N Anderson
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2010
Materias:
R
Q
Acceso en línea:https://doaj.org/article/6336e6c4ee3941a1be223c2fa5f9d714
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:6336e6c4ee3941a1be223c2fa5f9d714
record_format dspace
spelling oai:doaj.org-article:6336e6c4ee3941a1be223c2fa5f9d7142021-12-02T20:21:12ZOligonucleotide sequence motifs as nucleosome positioning signals.1932-620310.1371/journal.pone.0010933https://doaj.org/article/6336e6c4ee3941a1be223c2fa5f9d7142010-06-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20532171/?tool=EBIhttps://doaj.org/toc/1932-6203To gain a better understanding of the sequence patterns that characterize positioned nucleosomes, we first performed an analysis of the periodicities of the 256 tetranucleotides in a yeast genome-wide library of nucleosomal DNA sequences that was prepared by in vitro reconstitution. The approach entailed the identification and analysis of 24 unique tetranucleotides that were defined by 8 consensus sequences. These consensus sequences were shown to be responsible for most if not all of the tetranucleotide and dinucleotide periodicities displayed by the entire library, demonstrating that the periodicities of dinucleotides that characterize the yeast genome are, in actuality, due primarily to the 8 consensus sequences. A novel combination of experimental and bioinformatic approaches was then used to show that these tetranucleotides are important for preferred formation of nucleosomes at specific sites along DNA in vitro. These results were then compared to tetranucleotide patterns in genome-wide in vivo libraries from yeast and C. elegans in order to assess the contributions of DNA sequence in the control of nucleosome residency in the cell. These comparisons revealed striking similarities in the tetranucleotide occurrence profiles that are likely to be involved in nucleosome positioning in both in vitro and in vivo libraries, suggesting that DNA sequence is an important factor in the control of nucleosome placement in vivo. However, the strengths of the tetranucleotide periodicities were 3-4 fold higher in the in vitro as compared to the in vivo libraries, which implies that DNA sequence plays less of a role in dictating nucleosome positions in vivo. The results of this study have important implications for models of sequence-dependent positioning since they suggest that a defined subset of tetranucleotides is involved in preferred nucleosome occupancy and that these tetranucleotides are the major source of the dinucleotide periodicities that are characteristic of positioned nucleosomes.Clayton K CollingsAlfonso G FernandezChad G PitschkaTroy B HawkinsJohn N AndersonPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 5, Iss 6, p e10933 (2010)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Clayton K Collings
Alfonso G Fernandez
Chad G Pitschka
Troy B Hawkins
John N Anderson
Oligonucleotide sequence motifs as nucleosome positioning signals.
description To gain a better understanding of the sequence patterns that characterize positioned nucleosomes, we first performed an analysis of the periodicities of the 256 tetranucleotides in a yeast genome-wide library of nucleosomal DNA sequences that was prepared by in vitro reconstitution. The approach entailed the identification and analysis of 24 unique tetranucleotides that were defined by 8 consensus sequences. These consensus sequences were shown to be responsible for most if not all of the tetranucleotide and dinucleotide periodicities displayed by the entire library, demonstrating that the periodicities of dinucleotides that characterize the yeast genome are, in actuality, due primarily to the 8 consensus sequences. A novel combination of experimental and bioinformatic approaches was then used to show that these tetranucleotides are important for preferred formation of nucleosomes at specific sites along DNA in vitro. These results were then compared to tetranucleotide patterns in genome-wide in vivo libraries from yeast and C. elegans in order to assess the contributions of DNA sequence in the control of nucleosome residency in the cell. These comparisons revealed striking similarities in the tetranucleotide occurrence profiles that are likely to be involved in nucleosome positioning in both in vitro and in vivo libraries, suggesting that DNA sequence is an important factor in the control of nucleosome placement in vivo. However, the strengths of the tetranucleotide periodicities were 3-4 fold higher in the in vitro as compared to the in vivo libraries, which implies that DNA sequence plays less of a role in dictating nucleosome positions in vivo. The results of this study have important implications for models of sequence-dependent positioning since they suggest that a defined subset of tetranucleotides is involved in preferred nucleosome occupancy and that these tetranucleotides are the major source of the dinucleotide periodicities that are characteristic of positioned nucleosomes.
format article
author Clayton K Collings
Alfonso G Fernandez
Chad G Pitschka
Troy B Hawkins
John N Anderson
author_facet Clayton K Collings
Alfonso G Fernandez
Chad G Pitschka
Troy B Hawkins
John N Anderson
author_sort Clayton K Collings
title Oligonucleotide sequence motifs as nucleosome positioning signals.
title_short Oligonucleotide sequence motifs as nucleosome positioning signals.
title_full Oligonucleotide sequence motifs as nucleosome positioning signals.
title_fullStr Oligonucleotide sequence motifs as nucleosome positioning signals.
title_full_unstemmed Oligonucleotide sequence motifs as nucleosome positioning signals.
title_sort oligonucleotide sequence motifs as nucleosome positioning signals.
publisher Public Library of Science (PLoS)
publishDate 2010
url https://doaj.org/article/6336e6c4ee3941a1be223c2fa5f9d714
work_keys_str_mv AT claytonkcollings oligonucleotidesequencemotifsasnucleosomepositioningsignals
AT alfonsogfernandez oligonucleotidesequencemotifsasnucleosomepositioningsignals
AT chadgpitschka oligonucleotidesequencemotifsasnucleosomepositioningsignals
AT troybhawkins oligonucleotidesequencemotifsasnucleosomepositioningsignals
AT johnnanderson oligonucleotidesequencemotifsasnucleosomepositioningsignals
_version_ 1718374110978899968