Cargando…

Functional Analysis of the Molecular Interactions of TATA Box-Containing Genes and Essential Genes

Genes can be divided into TATA-containing genes and TATA-less genes according to the presence of TATA box elements at promoter regions. TATA-containing genes tend to be stress-responsive, whereas many TATA-less genes are known to be related to cell growth or “housekeeping” functions. In a previous s...

Descripción completa

Detalles Bibliográficos
Autores principales: Bae, Sang-Hun, Han, Hyun Wook, Moon, Jisook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366266/
https://www.ncbi.nlm.nih.gov/pubmed/25789484
http://dx.doi.org/10.1371/journal.pone.0120848
_version_ 1782362349454229504
author Bae, Sang-Hun
Han, Hyun Wook
Moon, Jisook
author_facet Bae, Sang-Hun
Han, Hyun Wook
Moon, Jisook
author_sort Bae, Sang-Hun
collection PubMed
description Genes can be divided into TATA-containing genes and TATA-less genes according to the presence of TATA box elements at promoter regions. TATA-containing genes tend to be stress-responsive, whereas many TATA-less genes are known to be related to cell growth or “housekeeping” functions. In a previous study, we demonstrated that there are striking differences among four gene sets defined by the presence of TATA box (TATA-containing) and essentiality (TATA-less) with respect to number of associated transcription factors, amino acid usage, and functional annotation. Extending this research in yeast, we identified KEGG (Kyoto Encyclopedia of Genes and Genomes) pathways that are statistically enriched in TATA-containing or TATA-less genes and evaluated the possibility that the enriched pathways are related to stress or growth as reflected by the individual functions of the genes involved. According to their enrichment for either of these two gene sets, we sorted KEGG pathways into TATA-containing-gene-enriched pathways (TEPs) and essential-gene-enriched pathways (EEPs). As expected, genes in TEPs and EEPs exhibited opposite results in terms of functional category, transcriptional regulation, codon adaptation index, and network properties, suggesting the possibility that the bipolar patterns in these pathways also contribute to the regulation of the stress response and to cell survival. Our findings provide the novel insight that significant enrichment of TATA-binding or TATA-less genes defines pathways as stress-responsive or growth-related.
format Online
Article
Text
id pubmed-4366266
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-43662662015-03-23 Functional Analysis of the Molecular Interactions of TATA Box-Containing Genes and Essential Genes Bae, Sang-Hun Han, Hyun Wook Moon, Jisook PLoS One Research Article Genes can be divided into TATA-containing genes and TATA-less genes according to the presence of TATA box elements at promoter regions. TATA-containing genes tend to be stress-responsive, whereas many TATA-less genes are known to be related to cell growth or “housekeeping” functions. In a previous study, we demonstrated that there are striking differences among four gene sets defined by the presence of TATA box (TATA-containing) and essentiality (TATA-less) with respect to number of associated transcription factors, amino acid usage, and functional annotation. Extending this research in yeast, we identified KEGG (Kyoto Encyclopedia of Genes and Genomes) pathways that are statistically enriched in TATA-containing or TATA-less genes and evaluated the possibility that the enriched pathways are related to stress or growth as reflected by the individual functions of the genes involved. According to their enrichment for either of these two gene sets, we sorted KEGG pathways into TATA-containing-gene-enriched pathways (TEPs) and essential-gene-enriched pathways (EEPs). As expected, genes in TEPs and EEPs exhibited opposite results in terms of functional category, transcriptional regulation, codon adaptation index, and network properties, suggesting the possibility that the bipolar patterns in these pathways also contribute to the regulation of the stress response and to cell survival. Our findings provide the novel insight that significant enrichment of TATA-binding or TATA-less genes defines pathways as stress-responsive or growth-related. Public Library of Science 2015-03-19 /pmc/articles/PMC4366266/ /pubmed/25789484 http://dx.doi.org/10.1371/journal.pone.0120848 Text en © 2015 Bae et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bae, Sang-Hun
Han, Hyun Wook
Moon, Jisook
Functional Analysis of the Molecular Interactions of TATA Box-Containing Genes and Essential Genes
title Functional Analysis of the Molecular Interactions of TATA Box-Containing Genes and Essential Genes
title_full Functional Analysis of the Molecular Interactions of TATA Box-Containing Genes and Essential Genes
title_fullStr Functional Analysis of the Molecular Interactions of TATA Box-Containing Genes and Essential Genes
title_full_unstemmed Functional Analysis of the Molecular Interactions of TATA Box-Containing Genes and Essential Genes
title_short Functional Analysis of the Molecular Interactions of TATA Box-Containing Genes and Essential Genes
title_sort functional analysis of the molecular interactions of tata box-containing genes and essential genes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366266/
https://www.ncbi.nlm.nih.gov/pubmed/25789484
http://dx.doi.org/10.1371/journal.pone.0120848
work_keys_str_mv AT baesanghun functionalanalysisofthemolecularinteractionsoftataboxcontaininggenesandessentialgenes
AT hanhyunwook functionalanalysisofthemolecularinteractionsoftataboxcontaininggenesandessentialgenes
AT moonjisook functionalanalysisofthemolecularinteractionsoftataboxcontaininggenesandessentialgenes