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Identifying the Combinatorial Effects of Histone Modifications by Association Rule Mining in Yeast
Eukaryotic genomes are packaged into chromatin by histone proteins whose chemical modification can profoundly influence gene expression. The histone modifications often act in combinations, which exert different effects on gene expression. Although a number of experimental techniques and data analys...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Libertas Academica
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2964047/ https://www.ncbi.nlm.nih.gov/pubmed/21037963 |
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author | Wang, Jiang Dai, Xianhua Xiang, Qian Deng, Yangyang Feng, Jihua Dai, Zhiming He, Caisheng |
author_facet | Wang, Jiang Dai, Xianhua Xiang, Qian Deng, Yangyang Feng, Jihua Dai, Zhiming He, Caisheng |
author_sort | Wang, Jiang |
collection | PubMed |
description | Eukaryotic genomes are packaged into chromatin by histone proteins whose chemical modification can profoundly influence gene expression. The histone modifications often act in combinations, which exert different effects on gene expression. Although a number of experimental techniques and data analysis methods have been developed to study histone modifications, it is still very difficult to identify the relationships among histone modifications on a genome-wide scale. We proposed a method to identify the combinatorial effects of histone modifications by association rule mining. The method first identified Functional Modification Transactions (FMTs) and then employed association rule mining algorithm and statistics methods to identify histone modification patterns. We applied the proposed methodology to Pokholok et al’s data with eight sets of histone modifications and Kurdistani et al’s data with eleven histone acetylation sites. Our method succeeds in revealing two different global views of histone modification landscapes on two datasets and identifying a number of modification patterns some of which are supported by previous studies. We concentrate on combinatorial effects of histone modifications which significantly affect gene expression. Our method succeeds in identifying known interactions among histone modifications and uncovering many previously unknown patterns. After in-depth analysis of possible mechanism by which histone modification patterns can alter transcriptional states, we infer three possible modification pattern reading mechanism (‘redundant’, ‘trivial’, ‘dominative’). Our results demonstrate several histone modification patterns which show significant correspondence between yeast and human cells. |
format | Text |
id | pubmed-2964047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Libertas Academica |
record_format | MEDLINE/PubMed |
spelling | pubmed-29640472010-10-29 Identifying the Combinatorial Effects of Histone Modifications by Association Rule Mining in Yeast Wang, Jiang Dai, Xianhua Xiang, Qian Deng, Yangyang Feng, Jihua Dai, Zhiming He, Caisheng Evol Bioinform Online Original Research Eukaryotic genomes are packaged into chromatin by histone proteins whose chemical modification can profoundly influence gene expression. The histone modifications often act in combinations, which exert different effects on gene expression. Although a number of experimental techniques and data analysis methods have been developed to study histone modifications, it is still very difficult to identify the relationships among histone modifications on a genome-wide scale. We proposed a method to identify the combinatorial effects of histone modifications by association rule mining. The method first identified Functional Modification Transactions (FMTs) and then employed association rule mining algorithm and statistics methods to identify histone modification patterns. We applied the proposed methodology to Pokholok et al’s data with eight sets of histone modifications and Kurdistani et al’s data with eleven histone acetylation sites. Our method succeeds in revealing two different global views of histone modification landscapes on two datasets and identifying a number of modification patterns some of which are supported by previous studies. We concentrate on combinatorial effects of histone modifications which significantly affect gene expression. Our method succeeds in identifying known interactions among histone modifications and uncovering many previously unknown patterns. After in-depth analysis of possible mechanism by which histone modification patterns can alter transcriptional states, we infer three possible modification pattern reading mechanism (‘redundant’, ‘trivial’, ‘dominative’). Our results demonstrate several histone modification patterns which show significant correspondence between yeast and human cells. Libertas Academica 2010-09-20 /pmc/articles/PMC2964047/ /pubmed/21037963 Text en © 2010 the author(s), publisher and licensee Libertas Academica Ltd. This is an open access article. Unrestricted non-commercial use is permitted provided the original work is properly cited. |
spellingShingle | Original Research Wang, Jiang Dai, Xianhua Xiang, Qian Deng, Yangyang Feng, Jihua Dai, Zhiming He, Caisheng Identifying the Combinatorial Effects of Histone Modifications by Association Rule Mining in Yeast |
title | Identifying the Combinatorial Effects of Histone Modifications by Association Rule Mining in Yeast |
title_full | Identifying the Combinatorial Effects of Histone Modifications by Association Rule Mining in Yeast |
title_fullStr | Identifying the Combinatorial Effects of Histone Modifications by Association Rule Mining in Yeast |
title_full_unstemmed | Identifying the Combinatorial Effects of Histone Modifications by Association Rule Mining in Yeast |
title_short | Identifying the Combinatorial Effects of Histone Modifications by Association Rule Mining in Yeast |
title_sort | identifying the combinatorial effects of histone modifications by association rule mining in yeast |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2964047/ https://www.ncbi.nlm.nih.gov/pubmed/21037963 |
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