Cargando…
Transcription-dependent spatial arrangements of CFTR and adjacent genes in human cell nuclei
We investigated in different human cell types nuclear positioning and transcriptional regulation of the functionally unrelated genes GASZ, CFTR, and CORTBP2, mapping to adjacent loci on human chromosome 7q31. When inactive, GASZ, CFTR, and CORTBP2 preferentially associated with the nuclear periphery...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2004
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172106/ https://www.ncbi.nlm.nih.gov/pubmed/15364959 http://dx.doi.org/10.1083/jcb.200404107 |
_version_ | 1782145015364976640 |
---|---|
author | Zink, Daniele Amaral, Margarida D. Englmann, Andreas Lang, Susanne Clarke, Luka A. Rudolph, Carsten Alt, Felix Luther, Kathrin Braz, Carla Sadoni, Nicolas Rosenecker, Joseph Schindelhauer, Dirk |
author_facet | Zink, Daniele Amaral, Margarida D. Englmann, Andreas Lang, Susanne Clarke, Luka A. Rudolph, Carsten Alt, Felix Luther, Kathrin Braz, Carla Sadoni, Nicolas Rosenecker, Joseph Schindelhauer, Dirk |
author_sort | Zink, Daniele |
collection | PubMed |
description | We investigated in different human cell types nuclear positioning and transcriptional regulation of the functionally unrelated genes GASZ, CFTR, and CORTBP2, mapping to adjacent loci on human chromosome 7q31. When inactive, GASZ, CFTR, and CORTBP2 preferentially associated with the nuclear periphery and with perinuclear heterochromatin, whereas in their actively transcribed states the gene loci preferentially associated with euchromatin in the nuclear interior. Adjacent genes associated simultaneously with these distinct chromatin fractions localizing at different nuclear regions, in accordance with their individual transcriptional regulation. Although the nuclear localization of CFTR changed after altering its transcription levels, the transcriptional status of CFTR was not changed by driving this gene into a different nuclear environment. This implied that the transcriptional activity affected the nuclear positioning, and not vice versa. Together, the results show that small chromosomal subregions can display highly flexible nuclear organizations that are regulated at the level of individual genes in a transcription-dependent manner. |
format | Text |
id | pubmed-2172106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21721062008-03-05 Transcription-dependent spatial arrangements of CFTR and adjacent genes in human cell nuclei Zink, Daniele Amaral, Margarida D. Englmann, Andreas Lang, Susanne Clarke, Luka A. Rudolph, Carsten Alt, Felix Luther, Kathrin Braz, Carla Sadoni, Nicolas Rosenecker, Joseph Schindelhauer, Dirk J Cell Biol Research Articles We investigated in different human cell types nuclear positioning and transcriptional regulation of the functionally unrelated genes GASZ, CFTR, and CORTBP2, mapping to adjacent loci on human chromosome 7q31. When inactive, GASZ, CFTR, and CORTBP2 preferentially associated with the nuclear periphery and with perinuclear heterochromatin, whereas in their actively transcribed states the gene loci preferentially associated with euchromatin in the nuclear interior. Adjacent genes associated simultaneously with these distinct chromatin fractions localizing at different nuclear regions, in accordance with their individual transcriptional regulation. Although the nuclear localization of CFTR changed after altering its transcription levels, the transcriptional status of CFTR was not changed by driving this gene into a different nuclear environment. This implied that the transcriptional activity affected the nuclear positioning, and not vice versa. Together, the results show that small chromosomal subregions can display highly flexible nuclear organizations that are regulated at the level of individual genes in a transcription-dependent manner. The Rockefeller University Press 2004-09-13 /pmc/articles/PMC2172106/ /pubmed/15364959 http://dx.doi.org/10.1083/jcb.200404107 Text en Copyright © 2004, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Zink, Daniele Amaral, Margarida D. Englmann, Andreas Lang, Susanne Clarke, Luka A. Rudolph, Carsten Alt, Felix Luther, Kathrin Braz, Carla Sadoni, Nicolas Rosenecker, Joseph Schindelhauer, Dirk Transcription-dependent spatial arrangements of CFTR and adjacent genes in human cell nuclei |
title | Transcription-dependent spatial arrangements of CFTR and adjacent genes in human cell nuclei |
title_full | Transcription-dependent spatial arrangements of CFTR and adjacent genes in human cell nuclei |
title_fullStr | Transcription-dependent spatial arrangements of CFTR and adjacent genes in human cell nuclei |
title_full_unstemmed | Transcription-dependent spatial arrangements of CFTR and adjacent genes in human cell nuclei |
title_short | Transcription-dependent spatial arrangements of CFTR and adjacent genes in human cell nuclei |
title_sort | transcription-dependent spatial arrangements of cftr and adjacent genes in human cell nuclei |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172106/ https://www.ncbi.nlm.nih.gov/pubmed/15364959 http://dx.doi.org/10.1083/jcb.200404107 |
work_keys_str_mv | AT zinkdaniele transcriptiondependentspatialarrangementsofcftrandadjacentgenesinhumancellnuclei AT amaralmargaridad transcriptiondependentspatialarrangementsofcftrandadjacentgenesinhumancellnuclei AT englmannandreas transcriptiondependentspatialarrangementsofcftrandadjacentgenesinhumancellnuclei AT langsusanne transcriptiondependentspatialarrangementsofcftrandadjacentgenesinhumancellnuclei AT clarkelukaa transcriptiondependentspatialarrangementsofcftrandadjacentgenesinhumancellnuclei AT rudolphcarsten transcriptiondependentspatialarrangementsofcftrandadjacentgenesinhumancellnuclei AT altfelix transcriptiondependentspatialarrangementsofcftrandadjacentgenesinhumancellnuclei AT lutherkathrin transcriptiondependentspatialarrangementsofcftrandadjacentgenesinhumancellnuclei AT brazcarla transcriptiondependentspatialarrangementsofcftrandadjacentgenesinhumancellnuclei AT sadoninicolas transcriptiondependentspatialarrangementsofcftrandadjacentgenesinhumancellnuclei AT roseneckerjoseph transcriptiondependentspatialarrangementsofcftrandadjacentgenesinhumancellnuclei AT schindelhauerdirk transcriptiondependentspatialarrangementsofcftrandadjacentgenesinhumancellnuclei |