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Interactions of MCP1 with Components of the Replication Machinery in Mammalian Cells
Eukaryotic DNA replication starts with the assembly of a pre-replication complex (pre-RC) at replication origins. We have previously demonstrated that Metaphase Chromosome Protein 1 (MCP1) is involved in the early events of DNA replication. Here we show that MCP1 associates with proteins that are re...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048848/ https://www.ncbi.nlm.nih.gov/pubmed/21383955 |
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author | Bronze-da-Rocha, Elsa Lin, Chii-Mei Shimura, Tsutomu Aladjem, Mirit I. |
author_facet | Bronze-da-Rocha, Elsa Lin, Chii-Mei Shimura, Tsutomu Aladjem, Mirit I. |
author_sort | Bronze-da-Rocha, Elsa |
collection | PubMed |
description | Eukaryotic DNA replication starts with the assembly of a pre-replication complex (pre-RC) at replication origins. We have previously demonstrated that Metaphase Chromosome Protein 1 (MCP1) is involved in the early events of DNA replication. Here we show that MCP1 associates with proteins that are required for the establishment of the pre-replication complex. Reciprocal immunoprecipitation analysis showed that MCP1 interacted with Cdc6, ORC2, ORC4, MCM2, MCM3 and MCM7, with Cdc45 and PCNA. Immunofluorescence studies demonstrated the co-localization of MCP1 with some of those proteins. Moreover, biochemical studies utilizing chromatin-immunoprecipitation (ChIP) revealed that MCP1 preferentially binds replication initiation sites in human cells. Interestingly, although members of the pre-RC are known to interact with some hallmarks of heterochromatin, our co-immunoprecipitation and immunofluorescence analyses showed that MCP1 did not interact and did not co-localize with heterochromatic proteins including HP1β and MetH3K9. These observations suggest that MCP1 is associated with replication factors required for the initiation of DNA replication and binds to the initiation sites in loci that replicate early in S-phase. In addition, immunological assays revealed the association of MCP1 forms with histone H1 variants and mass spectrometry analysis confirmed that MCP1 peptides share common sequences with H1.2 and H1.5 subtypes. |
format | Text |
id | pubmed-3048848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-30488482011-03-07 Interactions of MCP1 with Components of the Replication Machinery in Mammalian Cells Bronze-da-Rocha, Elsa Lin, Chii-Mei Shimura, Tsutomu Aladjem, Mirit I. Int J Biol Sci Research Paper Eukaryotic DNA replication starts with the assembly of a pre-replication complex (pre-RC) at replication origins. We have previously demonstrated that Metaphase Chromosome Protein 1 (MCP1) is involved in the early events of DNA replication. Here we show that MCP1 associates with proteins that are required for the establishment of the pre-replication complex. Reciprocal immunoprecipitation analysis showed that MCP1 interacted with Cdc6, ORC2, ORC4, MCM2, MCM3 and MCM7, with Cdc45 and PCNA. Immunofluorescence studies demonstrated the co-localization of MCP1 with some of those proteins. Moreover, biochemical studies utilizing chromatin-immunoprecipitation (ChIP) revealed that MCP1 preferentially binds replication initiation sites in human cells. Interestingly, although members of the pre-RC are known to interact with some hallmarks of heterochromatin, our co-immunoprecipitation and immunofluorescence analyses showed that MCP1 did not interact and did not co-localize with heterochromatic proteins including HP1β and MetH3K9. These observations suggest that MCP1 is associated with replication factors required for the initiation of DNA replication and binds to the initiation sites in loci that replicate early in S-phase. In addition, immunological assays revealed the association of MCP1 forms with histone H1 variants and mass spectrometry analysis confirmed that MCP1 peptides share common sequences with H1.2 and H1.5 subtypes. Ivyspring International Publisher 2011-02-17 /pmc/articles/PMC3048848/ /pubmed/21383955 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. |
spellingShingle | Research Paper Bronze-da-Rocha, Elsa Lin, Chii-Mei Shimura, Tsutomu Aladjem, Mirit I. Interactions of MCP1 with Components of the Replication Machinery in Mammalian Cells |
title | Interactions of MCP1 with Components of the Replication Machinery in Mammalian Cells |
title_full | Interactions of MCP1 with Components of the Replication Machinery in Mammalian Cells |
title_fullStr | Interactions of MCP1 with Components of the Replication Machinery in Mammalian Cells |
title_full_unstemmed | Interactions of MCP1 with Components of the Replication Machinery in Mammalian Cells |
title_short | Interactions of MCP1 with Components of the Replication Machinery in Mammalian Cells |
title_sort | interactions of mcp1 with components of the replication machinery in mammalian cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048848/ https://www.ncbi.nlm.nih.gov/pubmed/21383955 |
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