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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...

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Autores principales: Guenatri, Mounia, Bailly, Delphine, Maison, Christèle, Almouzni, Geneviève
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
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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.
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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
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