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Specific nuclear envelope transmembrane proteins can promote the location of chromosomes to and from the nuclear periphery
BACKGROUND: Different cell types have distinctive patterns of chromosome positioning in the nucleus. Although ectopic affinity-tethering of specific loci can be used to relocate chromosomes to the nuclear periphery, endogenous nuclear envelope proteins that control such a mechanism in mammalian cell...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053941/ https://www.ncbi.nlm.nih.gov/pubmed/23414781 http://dx.doi.org/10.1186/gb-2013-14-2-r14 |
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author | Zuleger, Nikolaj Boyle, Shelagh Kelly, David A de las Heras, Jose I Lazou, Vassiliki Korfali, Nadia Batrakou, Dzmitry G Randles, K Natalie Morris, Glenn E Harrison, David J Bickmore, Wendy A Schirmer, Eric C |
author_facet | Zuleger, Nikolaj Boyle, Shelagh Kelly, David A de las Heras, Jose I Lazou, Vassiliki Korfali, Nadia Batrakou, Dzmitry G Randles, K Natalie Morris, Glenn E Harrison, David J Bickmore, Wendy A Schirmer, Eric C |
author_sort | Zuleger, Nikolaj |
collection | PubMed |
description | BACKGROUND: Different cell types have distinctive patterns of chromosome positioning in the nucleus. Although ectopic affinity-tethering of specific loci can be used to relocate chromosomes to the nuclear periphery, endogenous nuclear envelope proteins that control such a mechanism in mammalian cells have yet to be widely identified. RESULTS: To search for such proteins, 23 nuclear envelope transmembrane proteins were screened for their ability to promote peripheral localization of human chromosomes in HT1080 fibroblasts. Five of these proteins had strong effects on chromosome 5, but individual proteins affected different subsets of chromosomes. The repositioning effects were reversible and the proteins with effects all exhibited highly tissue-restricted patterns of expression. Depletion of two nuclear envelope transmembrane proteins that were preferentially expressed in liver each reduced the normal peripheral positioning of chromosome 5 in liver cells. CONCLUSIONS: The discovery of nuclear envelope transmembrane proteins that can modulate chromosome position and have restricted patterns of expression may enable dissection of the functional relevance of tissue-specific patterns of radial chromosome positioning. |
format | Online Article Text |
id | pubmed-4053941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40539412014-06-12 Specific nuclear envelope transmembrane proteins can promote the location of chromosomes to and from the nuclear periphery Zuleger, Nikolaj Boyle, Shelagh Kelly, David A de las Heras, Jose I Lazou, Vassiliki Korfali, Nadia Batrakou, Dzmitry G Randles, K Natalie Morris, Glenn E Harrison, David J Bickmore, Wendy A Schirmer, Eric C Genome Biol Research BACKGROUND: Different cell types have distinctive patterns of chromosome positioning in the nucleus. Although ectopic affinity-tethering of specific loci can be used to relocate chromosomes to the nuclear periphery, endogenous nuclear envelope proteins that control such a mechanism in mammalian cells have yet to be widely identified. RESULTS: To search for such proteins, 23 nuclear envelope transmembrane proteins were screened for their ability to promote peripheral localization of human chromosomes in HT1080 fibroblasts. Five of these proteins had strong effects on chromosome 5, but individual proteins affected different subsets of chromosomes. The repositioning effects were reversible and the proteins with effects all exhibited highly tissue-restricted patterns of expression. Depletion of two nuclear envelope transmembrane proteins that were preferentially expressed in liver each reduced the normal peripheral positioning of chromosome 5 in liver cells. CONCLUSIONS: The discovery of nuclear envelope transmembrane proteins that can modulate chromosome position and have restricted patterns of expression may enable dissection of the functional relevance of tissue-specific patterns of radial chromosome positioning. BioMed Central 2013 2013-02-15 /pmc/articles/PMC4053941/ /pubmed/23414781 http://dx.doi.org/10.1186/gb-2013-14-2-r14 Text en Copyright © 2013 Zuleger et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Zuleger, Nikolaj Boyle, Shelagh Kelly, David A de las Heras, Jose I Lazou, Vassiliki Korfali, Nadia Batrakou, Dzmitry G Randles, K Natalie Morris, Glenn E Harrison, David J Bickmore, Wendy A Schirmer, Eric C Specific nuclear envelope transmembrane proteins can promote the location of chromosomes to and from the nuclear periphery |
title | Specific nuclear envelope transmembrane proteins can promote the location of chromosomes to and from the nuclear periphery |
title_full | Specific nuclear envelope transmembrane proteins can promote the location of chromosomes to and from the nuclear periphery |
title_fullStr | Specific nuclear envelope transmembrane proteins can promote the location of chromosomes to and from the nuclear periphery |
title_full_unstemmed | Specific nuclear envelope transmembrane proteins can promote the location of chromosomes to and from the nuclear periphery |
title_short | Specific nuclear envelope transmembrane proteins can promote the location of chromosomes to and from the nuclear periphery |
title_sort | specific nuclear envelope transmembrane proteins can promote the location of chromosomes to and from the nuclear periphery |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053941/ https://www.ncbi.nlm.nih.gov/pubmed/23414781 http://dx.doi.org/10.1186/gb-2013-14-2-r14 |
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