Cargando…
Fission Yeast CENP-C (Cnp3) Plays a Role in Restricting the Site of CENP-A Accumulation
The centromere is a chromosomal locus where a microtubule attachment site, termed kinetochore, is assembled in mitosis. In most eukaryotes, with the exception of holocentric species, each chromosome contains a single distinct centromere. A chromosome with an additional centromere undergoes successiv...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071599/ https://www.ncbi.nlm.nih.gov/pubmed/29925533 http://dx.doi.org/10.1534/g3.118.200486 |
_version_ | 1783343898026835968 |
---|---|
author | Suma, Michiko Kitagawa, Teppei Nakase, Yukiko Nakazawa, Norihiko Yanagida, Mitsuhiro Matsumoto, Tomohiro |
author_facet | Suma, Michiko Kitagawa, Teppei Nakase, Yukiko Nakazawa, Norihiko Yanagida, Mitsuhiro Matsumoto, Tomohiro |
author_sort | Suma, Michiko |
collection | PubMed |
description | The centromere is a chromosomal locus where a microtubule attachment site, termed kinetochore, is assembled in mitosis. In most eukaryotes, with the exception of holocentric species, each chromosome contains a single distinct centromere. A chromosome with an additional centromere undergoes successive rounds of anaphase bridge formation and breakage, or triggers a cell cycle arrest imposed by DNA damage and replication checkpoints. We report here a study in Schizosaccharomyces pombe to characterize a mutant (cnp3-1) in a gene encoding a homolog of mammalian centromere-specific protein, CENP-C. At the restrictive temperature 36°, the Cnp3-1 mutant protein loses its localization at the centromere. In the cnp3-1 mutant, the level of the Cnp1 (a homolog of a centromere-specific histone CENP-A) also decreases at the centromere. Interestingly, the cnp3-1 mutant is prone to promiscuous accumulation of Cnp1 at non-centromeric regions, when Cnp1 is present in excess. Unlike the wild type protein, Cnp3-1 mutant protein is found at the sites of promiscuous accumulation of Cnp1, suggesting that Cnp3-1 may stabilize or promote accumulation of Cnp1 at non-centromeric regions. From these results, we infer the role of Cnp3 in restricting the site of accumulation of Cnp1 and thus to prevent formation of de novo centromeres. |
format | Online Article Text |
id | pubmed-6071599 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-60715992018-08-03 Fission Yeast CENP-C (Cnp3) Plays a Role in Restricting the Site of CENP-A Accumulation Suma, Michiko Kitagawa, Teppei Nakase, Yukiko Nakazawa, Norihiko Yanagida, Mitsuhiro Matsumoto, Tomohiro G3 (Bethesda) Investigations The centromere is a chromosomal locus where a microtubule attachment site, termed kinetochore, is assembled in mitosis. In most eukaryotes, with the exception of holocentric species, each chromosome contains a single distinct centromere. A chromosome with an additional centromere undergoes successive rounds of anaphase bridge formation and breakage, or triggers a cell cycle arrest imposed by DNA damage and replication checkpoints. We report here a study in Schizosaccharomyces pombe to characterize a mutant (cnp3-1) in a gene encoding a homolog of mammalian centromere-specific protein, CENP-C. At the restrictive temperature 36°, the Cnp3-1 mutant protein loses its localization at the centromere. In the cnp3-1 mutant, the level of the Cnp1 (a homolog of a centromere-specific histone CENP-A) also decreases at the centromere. Interestingly, the cnp3-1 mutant is prone to promiscuous accumulation of Cnp1 at non-centromeric regions, when Cnp1 is present in excess. Unlike the wild type protein, Cnp3-1 mutant protein is found at the sites of promiscuous accumulation of Cnp1, suggesting that Cnp3-1 may stabilize or promote accumulation of Cnp1 at non-centromeric regions. From these results, we infer the role of Cnp3 in restricting the site of accumulation of Cnp1 and thus to prevent formation of de novo centromeres. Genetics Society of America 2018-06-20 /pmc/articles/PMC6071599/ /pubmed/29925533 http://dx.doi.org/10.1534/g3.118.200486 Text en Copyright © 2018 Suma et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigations Suma, Michiko Kitagawa, Teppei Nakase, Yukiko Nakazawa, Norihiko Yanagida, Mitsuhiro Matsumoto, Tomohiro Fission Yeast CENP-C (Cnp3) Plays a Role in Restricting the Site of CENP-A Accumulation |
title | Fission Yeast CENP-C (Cnp3) Plays a Role in Restricting the Site of CENP-A Accumulation |
title_full | Fission Yeast CENP-C (Cnp3) Plays a Role in Restricting the Site of CENP-A Accumulation |
title_fullStr | Fission Yeast CENP-C (Cnp3) Plays a Role in Restricting the Site of CENP-A Accumulation |
title_full_unstemmed | Fission Yeast CENP-C (Cnp3) Plays a Role in Restricting the Site of CENP-A Accumulation |
title_short | Fission Yeast CENP-C (Cnp3) Plays a Role in Restricting the Site of CENP-A Accumulation |
title_sort | fission yeast cenp-c (cnp3) plays a role in restricting the site of cenp-a accumulation |
topic | Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071599/ https://www.ncbi.nlm.nih.gov/pubmed/29925533 http://dx.doi.org/10.1534/g3.118.200486 |
work_keys_str_mv | AT sumamichiko fissionyeastcenpccnp3playsaroleinrestrictingthesiteofcenpaaccumulation AT kitagawateppei fissionyeastcenpccnp3playsaroleinrestrictingthesiteofcenpaaccumulation AT nakaseyukiko fissionyeastcenpccnp3playsaroleinrestrictingthesiteofcenpaaccumulation AT nakazawanorihiko fissionyeastcenpccnp3playsaroleinrestrictingthesiteofcenpaaccumulation AT yanagidamitsuhiro fissionyeastcenpccnp3playsaroleinrestrictingthesiteofcenpaaccumulation AT matsumototomohiro fissionyeastcenpccnp3playsaroleinrestrictingthesiteofcenpaaccumulation |