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DISC1 and Huntington's Disease – Overlapping Pathways of Vulnerability to Neurological Disorder?
We re-annotated the interacting partners of the neuronal scaffold protein DISC1 using a knowledge-based approach that incorporated recent protein interaction data and published literature to. This revealed two highly connected networks. These networks feature cellular function and maintenance, and c...
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3027647/ https://www.ncbi.nlm.nih.gov/pubmed/21298101 http://dx.doi.org/10.1371/journal.pone.0016263 |
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author | Boxall, Ruth Porteous, David J. Thomson, Pippa A. |
author_facet | Boxall, Ruth Porteous, David J. Thomson, Pippa A. |
author_sort | Boxall, Ruth |
collection | PubMed |
description | We re-annotated the interacting partners of the neuronal scaffold protein DISC1 using a knowledge-based approach that incorporated recent protein interaction data and published literature to. This revealed two highly connected networks. These networks feature cellular function and maintenance, and cell signaling. Of potentially greatest interest was the novel finding of a high degree of connectivity between the DISC1 scaffold protein, linked to psychiatric illness, and huntingtin, the protein which is mutated in Huntington's disease. The potential link between DISC1, huntingtin and their interacting partners may open new areas of research into the effects of pathway dysregulation in severe neurological disorders. |
format | Text |
id | pubmed-3027647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30276472011-02-04 DISC1 and Huntington's Disease – Overlapping Pathways of Vulnerability to Neurological Disorder? Boxall, Ruth Porteous, David J. Thomson, Pippa A. PLoS One Research Article We re-annotated the interacting partners of the neuronal scaffold protein DISC1 using a knowledge-based approach that incorporated recent protein interaction data and published literature to. This revealed two highly connected networks. These networks feature cellular function and maintenance, and cell signaling. Of potentially greatest interest was the novel finding of a high degree of connectivity between the DISC1 scaffold protein, linked to psychiatric illness, and huntingtin, the protein which is mutated in Huntington's disease. The potential link between DISC1, huntingtin and their interacting partners may open new areas of research into the effects of pathway dysregulation in severe neurological disorders. Public Library of Science 2011-01-26 /pmc/articles/PMC3027647/ /pubmed/21298101 http://dx.doi.org/10.1371/journal.pone.0016263 Text en Boxall 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 Boxall, Ruth Porteous, David J. Thomson, Pippa A. DISC1 and Huntington's Disease – Overlapping Pathways of Vulnerability to Neurological Disorder? |
title | DISC1 and Huntington's Disease – Overlapping Pathways of Vulnerability to Neurological Disorder? |
title_full | DISC1 and Huntington's Disease – Overlapping Pathways of Vulnerability to Neurological Disorder? |
title_fullStr | DISC1 and Huntington's Disease – Overlapping Pathways of Vulnerability to Neurological Disorder? |
title_full_unstemmed | DISC1 and Huntington's Disease – Overlapping Pathways of Vulnerability to Neurological Disorder? |
title_short | DISC1 and Huntington's Disease – Overlapping Pathways of Vulnerability to Neurological Disorder? |
title_sort | disc1 and huntington's disease – overlapping pathways of vulnerability to neurological disorder? |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3027647/ https://www.ncbi.nlm.nih.gov/pubmed/21298101 http://dx.doi.org/10.1371/journal.pone.0016263 |
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