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Two different classes of co-occurring motif pairs found by a novel visualization method in human promoter regions

BACKGROUND: It is essential in modern biology to understand how transcriptional regulatory regions are composed of cis-elements, yet we have limited knowledge of, for example, the combinational uses of these elements and their positional distribution. RESULTS: We predicted the positions of 228 known...

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Autores principales: Murakami, Katsuhiko, Imanishi, Tadashi, Gojobori, Takashi, Nakai, Kenta
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2292176/
https://www.ncbi.nlm.nih.gov/pubmed/18312685
http://dx.doi.org/10.1186/1471-2164-9-112
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author Murakami, Katsuhiko
Imanishi, Tadashi
Gojobori, Takashi
Nakai, Kenta
author_facet Murakami, Katsuhiko
Imanishi, Tadashi
Gojobori, Takashi
Nakai, Kenta
author_sort Murakami, Katsuhiko
collection PubMed
description BACKGROUND: It is essential in modern biology to understand how transcriptional regulatory regions are composed of cis-elements, yet we have limited knowledge of, for example, the combinational uses of these elements and their positional distribution. RESULTS: We predicted the positions of 228 known binding motifs for transcription factors in phylogenetically conserved regions within -2000 and +1000 bp of transcriptional start sites (TSSs) of human genes and visualized their correlated non-overlapping occurrences. In the 8,454 significantly correlated motif pairs, two major classes were observed: 248 pairs in Class 1 were mainly found around TSSs, whereas 4,020 Class 2 pairs appear at rather arbitrary distances from TSSs. These classes are distinct in a number of aspects. First, the positional distribution of the Class 1 constituent motifs shows a single peak near the TSSs, whereas Class 2 motifs show a relatively broad distribution. Second, genes that harbor the Class 1 pairs are more likely to be CpG-rich and to be expressed ubiquitously than those that harbor Class 2 pairs. Third, the 'hub' motifs, which are used in many different motif pairs, are different between the two classes. In addition, many of the transcription factors that correspond to the Class 2 hub motifs contain domains rich in specific amino acids; these domains may form disordered regions important for protein-protein interaction. CONCLUSION: There exist at least two classes of motif pairs with respect to TSSs in human promoters, possibly reflecting compositional differences between promoters and enhancers. We anticipate that our visualization method may be useful for the further characterisation of promoters.
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spelling pubmed-22921762008-04-11 Two different classes of co-occurring motif pairs found by a novel visualization method in human promoter regions Murakami, Katsuhiko Imanishi, Tadashi Gojobori, Takashi Nakai, Kenta BMC Genomics Research Article BACKGROUND: It is essential in modern biology to understand how transcriptional regulatory regions are composed of cis-elements, yet we have limited knowledge of, for example, the combinational uses of these elements and their positional distribution. RESULTS: We predicted the positions of 228 known binding motifs for transcription factors in phylogenetically conserved regions within -2000 and +1000 bp of transcriptional start sites (TSSs) of human genes and visualized their correlated non-overlapping occurrences. In the 8,454 significantly correlated motif pairs, two major classes were observed: 248 pairs in Class 1 were mainly found around TSSs, whereas 4,020 Class 2 pairs appear at rather arbitrary distances from TSSs. These classes are distinct in a number of aspects. First, the positional distribution of the Class 1 constituent motifs shows a single peak near the TSSs, whereas Class 2 motifs show a relatively broad distribution. Second, genes that harbor the Class 1 pairs are more likely to be CpG-rich and to be expressed ubiquitously than those that harbor Class 2 pairs. Third, the 'hub' motifs, which are used in many different motif pairs, are different between the two classes. In addition, many of the transcription factors that correspond to the Class 2 hub motifs contain domains rich in specific amino acids; these domains may form disordered regions important for protein-protein interaction. CONCLUSION: There exist at least two classes of motif pairs with respect to TSSs in human promoters, possibly reflecting compositional differences between promoters and enhancers. We anticipate that our visualization method may be useful for the further characterisation of promoters. BioMed Central 2008-03-01 /pmc/articles/PMC2292176/ /pubmed/18312685 http://dx.doi.org/10.1186/1471-2164-9-112 Text en Copyright © 2008 Murakami et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Murakami, Katsuhiko
Imanishi, Tadashi
Gojobori, Takashi
Nakai, Kenta
Two different classes of co-occurring motif pairs found by a novel visualization method in human promoter regions
title Two different classes of co-occurring motif pairs found by a novel visualization method in human promoter regions
title_full Two different classes of co-occurring motif pairs found by a novel visualization method in human promoter regions
title_fullStr Two different classes of co-occurring motif pairs found by a novel visualization method in human promoter regions
title_full_unstemmed Two different classes of co-occurring motif pairs found by a novel visualization method in human promoter regions
title_short Two different classes of co-occurring motif pairs found by a novel visualization method in human promoter regions
title_sort two different classes of co-occurring motif pairs found by a novel visualization method in human promoter regions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2292176/
https://www.ncbi.nlm.nih.gov/pubmed/18312685
http://dx.doi.org/10.1186/1471-2164-9-112
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