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Exploring the effects of polymorphisms on cis-regulatory signal transduction response
cis-Regulatory sequences (CRSs) direct cell-specific and inducible gene expression in response to signal transduction networks, and it is becoming apparent that many cases of disease susceptibility and drug response stratification are due to polymorphisms that alter CRS responses in a context-depend...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569712/ https://www.ncbi.nlm.nih.gov/pubmed/23265842 http://dx.doi.org/10.1016/j.molmed.2012.11.003 |
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author | MacKenzie, Alasdair Hing, Benjamin Davidson, Scott |
author_facet | MacKenzie, Alasdair Hing, Benjamin Davidson, Scott |
author_sort | MacKenzie, Alasdair |
collection | PubMed |
description | cis-Regulatory sequences (CRSs) direct cell-specific and inducible gene expression in response to signal transduction networks, and it is becoming apparent that many cases of disease susceptibility and drug response stratification are due to polymorphisms that alter CRS responses in a context-dependent manner. In the current review, we describe successful methods for identifying CRSs and analyzing the effects of allelic variation on their responses to signal transduction. The technologies described build on the successes of ENCODE (ENCyclopedia Of DNA Elements) by exploring the effects of polymorphisms on CRS context dependency. This understanding is essential to uncover the genomic basis of disease susceptibility and will play a major role in delivering on the promise of personalized medicine. |
format | Online Article Text |
id | pubmed-3569712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier Science Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-35697122013-02-12 Exploring the effects of polymorphisms on cis-regulatory signal transduction response MacKenzie, Alasdair Hing, Benjamin Davidson, Scott Trends Mol Med Review cis-Regulatory sequences (CRSs) direct cell-specific and inducible gene expression in response to signal transduction networks, and it is becoming apparent that many cases of disease susceptibility and drug response stratification are due to polymorphisms that alter CRS responses in a context-dependent manner. In the current review, we describe successful methods for identifying CRSs and analyzing the effects of allelic variation on their responses to signal transduction. The technologies described build on the successes of ENCODE (ENCyclopedia Of DNA Elements) by exploring the effects of polymorphisms on CRS context dependency. This understanding is essential to uncover the genomic basis of disease susceptibility and will play a major role in delivering on the promise of personalized medicine. Elsevier Science Ltd 2013-02 /pmc/articles/PMC3569712/ /pubmed/23265842 http://dx.doi.org/10.1016/j.molmed.2012.11.003 Text en © 2013 Elsevier Ltd. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Review MacKenzie, Alasdair Hing, Benjamin Davidson, Scott Exploring the effects of polymorphisms on cis-regulatory signal transduction response |
title | Exploring the effects of polymorphisms on cis-regulatory signal transduction response |
title_full | Exploring the effects of polymorphisms on cis-regulatory signal transduction response |
title_fullStr | Exploring the effects of polymorphisms on cis-regulatory signal transduction response |
title_full_unstemmed | Exploring the effects of polymorphisms on cis-regulatory signal transduction response |
title_short | Exploring the effects of polymorphisms on cis-regulatory signal transduction response |
title_sort | exploring the effects of polymorphisms on cis-regulatory signal transduction response |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569712/ https://www.ncbi.nlm.nih.gov/pubmed/23265842 http://dx.doi.org/10.1016/j.molmed.2012.11.003 |
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