Cargando…
Essentiality drives the orientation bias of bacterial genes in a continuous manner
Studies had found that bacterial genes are preferentially located on the leading strands. Subsequently, the preferences of essential genes and highly expressed genes were compared by classifying all genes into four groups, which showed that the former has an exclusive influence on orientation. Howev...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642330/ https://www.ncbi.nlm.nih.gov/pubmed/26560889 http://dx.doi.org/10.1038/srep16431 |
_version_ | 1782400344863539200 |
---|---|
author | Zheng, Wen-Xin Luo, Cheng-Si Deng, Yan-Yan Guo, Feng-Biao |
author_facet | Zheng, Wen-Xin Luo, Cheng-Si Deng, Yan-Yan Guo, Feng-Biao |
author_sort | Zheng, Wen-Xin |
collection | PubMed |
description | Studies had found that bacterial genes are preferentially located on the leading strands. Subsequently, the preferences of essential genes and highly expressed genes were compared by classifying all genes into four groups, which showed that the former has an exclusive influence on orientation. However, only some functional classes of essential genes have this orientation bias. Nevertheless, previous studies only performed comparative analyzes by differentiating the orientation bias extent of two types of genes. Thus, it is unclear whether the influence of essentiality on strand bias works continuously. Herein, we found a significant correlation between essentiality and orientation bias extent in 19 of 21 analyzed bacterial genomes, based on quantitative measurement of gene essentiality (or fitness). The correlation coefficient was much higher than that derived from binary essentiality measures (essential or non-essential). This suggested that genes with relatively lower essentiality, i.e., conditionally essential genes, also have some orientation bias, although it is weaker than that of absolutely essential genes. The results demonstrated the continuous influence of essentiality on orientation bias and provided details on this visible structural feature of bacterial genomes. It also proved that Geptop and IFIM could serve as useful resources of bacterial gene essentiality, particularly for quantitative analysis. |
format | Online Article Text |
id | pubmed-4642330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46423302015-11-20 Essentiality drives the orientation bias of bacterial genes in a continuous manner Zheng, Wen-Xin Luo, Cheng-Si Deng, Yan-Yan Guo, Feng-Biao Sci Rep Article Studies had found that bacterial genes are preferentially located on the leading strands. Subsequently, the preferences of essential genes and highly expressed genes were compared by classifying all genes into four groups, which showed that the former has an exclusive influence on orientation. However, only some functional classes of essential genes have this orientation bias. Nevertheless, previous studies only performed comparative analyzes by differentiating the orientation bias extent of two types of genes. Thus, it is unclear whether the influence of essentiality on strand bias works continuously. Herein, we found a significant correlation between essentiality and orientation bias extent in 19 of 21 analyzed bacterial genomes, based on quantitative measurement of gene essentiality (or fitness). The correlation coefficient was much higher than that derived from binary essentiality measures (essential or non-essential). This suggested that genes with relatively lower essentiality, i.e., conditionally essential genes, also have some orientation bias, although it is weaker than that of absolutely essential genes. The results demonstrated the continuous influence of essentiality on orientation bias and provided details on this visible structural feature of bacterial genomes. It also proved that Geptop and IFIM could serve as useful resources of bacterial gene essentiality, particularly for quantitative analysis. Nature Publishing Group 2015-11-12 /pmc/articles/PMC4642330/ /pubmed/26560889 http://dx.doi.org/10.1038/srep16431 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zheng, Wen-Xin Luo, Cheng-Si Deng, Yan-Yan Guo, Feng-Biao Essentiality drives the orientation bias of bacterial genes in a continuous manner |
title | Essentiality drives the orientation bias of bacterial genes in a continuous manner |
title_full | Essentiality drives the orientation bias of bacterial genes in a continuous manner |
title_fullStr | Essentiality drives the orientation bias of bacterial genes in a continuous manner |
title_full_unstemmed | Essentiality drives the orientation bias of bacterial genes in a continuous manner |
title_short | Essentiality drives the orientation bias of bacterial genes in a continuous manner |
title_sort | essentiality drives the orientation bias of bacterial genes in a continuous manner |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642330/ https://www.ncbi.nlm.nih.gov/pubmed/26560889 http://dx.doi.org/10.1038/srep16431 |
work_keys_str_mv | AT zhengwenxin essentialitydrivestheorientationbiasofbacterialgenesinacontinuousmanner AT luochengsi essentialitydrivestheorientationbiasofbacterialgenesinacontinuousmanner AT dengyanyan essentialitydrivestheorientationbiasofbacterialgenesinacontinuousmanner AT guofengbiao essentialitydrivestheorientationbiasofbacterialgenesinacontinuousmanner |