Skip Navigation


Bioinformatics Advance Access originally published online on March 15, 2005
Bioinformatics 2005 21(11):2623-2628; doi:10.1093/bioinformatics/bti387
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (Print PDF) Freely available
Right arrow All Versions of this Article:
21/11/2623    most recent
bti387v1
Right arrow Comments: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Comments are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (6)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Chowdhary, R.
Right arrow Articles by Bajic, V. B
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chowdhary, R.
Right arrow Articles by Bajic, V. B
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2005. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions{at}oupjournals.org

Promoter modeling: the case study of mammalian histone promoters

Rajesh Chowdhary 1, R. Ayesha Ali 2, Werner Albig 3, Detlef Doenecke 3 and Vladimir B Bajic 1,*

1Knowledge Extraction Lab, Institute for Infocomm Research 21 Heng Mui Keng Terrace, Singapore 119613
2Department of Statistics and Applied Probability, National University of Singapore 3 Science Drive 2, Singapore 117543
3Department of Molecular Biology, Biochemistry and Molecular Cell Biology, University of Göttingen Humboldtallee 23, 37073 Göttingen, Germany

*To whom correspondence should be addressed.

Motivation: Histone proteins play important roles in chromosomal functions. They are significantly evolutionarily conserved across species, which suggests similarity in their transcription regulation. The abundance of experimental data on histone promoters provides an excellent background for the evaluation of computational methods. Our study addresses the issue of how well computational analysis can contribute to unveiling the biologically relevant content of promoter regions for a large number of mammalian histone genes taken across several species, and suggests the consensus promoter models of different histone groups.

Results: This is the first study to unveil the detailed promoter structures of all five mammalian histone groups and their subgroups. This is also the most comprehensive computational analysis of histone promoters performed to date. The most exciting fact is that the results correlate very well with the biologically known facts and experimental data. Our analysis convincingly demonstrates that computational approach can significantly contribute to elucidation of promoter content (identification of biologically relevant signals) complementing tedious wet-lab experiments. We believe that this type of analysis can be easily applied to other functional gene classes, thus providing a general framework for modelling promoter groups. These results also provide the basis to hunt for genes co-regulated with histone genes across mammalian genomes.

Contact: bajicv{at}i2r.a-star.edu.sg

Supplementary information: http://research.i2r.a-star.edu.sg/promoter/histones/PubMed15769833.pdf


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Neurosci.Home page
A. B. James, A.-M. Conway, and B. J. Morris
Regulation of the Neuronal Proteasome by Zif268 (Egr1)
J. Neurosci., February 1, 2006; 26(5): 1624 - 1634.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.