Cargando…
Mouse centric and pericentric satellite repeats form distinct functional heterochromatin
Heterochromatin is thought to play a critical role for centromeric function. However, the respective contributions of the distinct repetitive sequences found in these regions, such as minor and major satellites in the mouse, have remained largely unsolved. We show that these centric and pericentric...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2004
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172221/ https://www.ncbi.nlm.nih.gov/pubmed/15302854 http://dx.doi.org/10.1083/jcb.200403109 |
_version_ | 1782145030314524672 |
---|---|
author | Guenatri, Mounia Bailly, Delphine Maison, Christèle Almouzni, Geneviève |
author_facet | Guenatri, Mounia Bailly, Delphine Maison, Christèle Almouzni, Geneviève |
author_sort | Guenatri, Mounia |
collection | PubMed |
description | Heterochromatin is thought to play a critical role for centromeric function. However, the respective contributions of the distinct repetitive sequences found in these regions, such as minor and major satellites in the mouse, have remained largely unsolved. We show that these centric and pericentric repeats on the chromosomes have distinct heterochromatic characteristics in the nucleus. Major satellites from different chromosomes form clusters associated with heterochromatin protein 1α, whereas minor satellites are individual entities associated with centromeric proteins. Both regions contain methylated histone H3 (Me-K9 H3) but show different micrococcal nuclease sensitivities. A dinucleosome repeating unit is found specifically associated with major satellites. These domains replicate asynchronously, and chromatid cohesion is sustained for a longer time in major satellites compared with minor satellites. Such prolonged cohesion in major satellites is lost in the absence of Suv39h histone methyltransferases. Thus, we define functionally independent centromeric subdomains, which spatio-temporal isolation is proposed to be important for centromeric cohesion and dissociation during chromosome segregation. |
format | Text |
id | pubmed-2172221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21722212008-03-05 Mouse centric and pericentric satellite repeats form distinct functional heterochromatin Guenatri, Mounia Bailly, Delphine Maison, Christèle Almouzni, Geneviève J Cell Biol Research Articles Heterochromatin is thought to play a critical role for centromeric function. However, the respective contributions of the distinct repetitive sequences found in these regions, such as minor and major satellites in the mouse, have remained largely unsolved. We show that these centric and pericentric repeats on the chromosomes have distinct heterochromatic characteristics in the nucleus. Major satellites from different chromosomes form clusters associated with heterochromatin protein 1α, whereas minor satellites are individual entities associated with centromeric proteins. Both regions contain methylated histone H3 (Me-K9 H3) but show different micrococcal nuclease sensitivities. A dinucleosome repeating unit is found specifically associated with major satellites. These domains replicate asynchronously, and chromatid cohesion is sustained for a longer time in major satellites compared with minor satellites. Such prolonged cohesion in major satellites is lost in the absence of Suv39h histone methyltransferases. Thus, we define functionally independent centromeric subdomains, which spatio-temporal isolation is proposed to be important for centromeric cohesion and dissociation during chromosome segregation. The Rockefeller University Press 2004-08-16 /pmc/articles/PMC2172221/ /pubmed/15302854 http://dx.doi.org/10.1083/jcb.200403109 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 Guenatri, Mounia Bailly, Delphine Maison, Christèle Almouzni, Geneviève Mouse centric and pericentric satellite repeats form distinct functional heterochromatin |
title | Mouse centric and pericentric satellite repeats form distinct functional heterochromatin |
title_full | Mouse centric and pericentric satellite repeats form distinct functional heterochromatin |
title_fullStr | Mouse centric and pericentric satellite repeats form distinct functional heterochromatin |
title_full_unstemmed | Mouse centric and pericentric satellite repeats form distinct functional heterochromatin |
title_short | Mouse centric and pericentric satellite repeats form distinct functional heterochromatin |
title_sort | mouse centric and pericentric satellite repeats form distinct functional heterochromatin |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172221/ https://www.ncbi.nlm.nih.gov/pubmed/15302854 http://dx.doi.org/10.1083/jcb.200403109 |
work_keys_str_mv | AT guenatrimounia mousecentricandpericentricsatelliterepeatsformdistinctfunctionalheterochromatin AT baillydelphine mousecentricandpericentricsatelliterepeatsformdistinctfunctionalheterochromatin AT maisonchristele mousecentricandpericentricsatelliterepeatsformdistinctfunctionalheterochromatin AT almouznigenevieve mousecentricandpericentricsatelliterepeatsformdistinctfunctionalheterochromatin |