Cargando…
Evidence for a Replication Function of Ffa-1, the Xenopus Orthologue of Werner Syndrome Protein
DNA replication in higher eukaryotic cells occurs at a large number of discrete sites called replication foci. We have previously purified a protein, focus-forming activity 1 (FFA-1), which is involved in the assembly of putative prereplication foci in Xenopus egg extracts. FFA-1 is the orthologue o...
Autores principales: | , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2001
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2198806/ https://www.ncbi.nlm.nih.gov/pubmed/11238454 |
_version_ | 1782148074818240512 |
---|---|
author | Chen, Chin-Yi Graham, Jeanine Yan, Hong |
author_facet | Chen, Chin-Yi Graham, Jeanine Yan, Hong |
author_sort | Chen, Chin-Yi |
collection | PubMed |
description | DNA replication in higher eukaryotic cells occurs at a large number of discrete sites called replication foci. We have previously purified a protein, focus-forming activity 1 (FFA-1), which is involved in the assembly of putative prereplication foci in Xenopus egg extracts. FFA-1 is the orthologue of the Werner syndrome gene product (WRN), a member of the RecQ helicase family. In this paper we show that FFA-1 colocalizes with sites of DNA synthesis and the single-stranded DNA binding protein, replication protein A (RPA), in nuclei reconstituted in the egg extract. In addition, we show that two glutathione S-transferase FFA-1 fusion proteins can inhibit DNA replication in a dominant negative manner. The dominant negative effect correlates with the incorporation of the fusion proteins into replication foci to form “hybrid foci,” which are unable to engage in DNA replication. At the biochemical level, RPA can interact with FFA-1 and specifically stimulates its DNA helicase activity. However, in the presence of the dominant negative mutant proteins, the stimulation is prevented. These results provide the first direct biochemical evidence of an important role for FFA-1 in DNA replication. |
format | Text |
id | pubmed-2198806 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21988062008-05-01 Evidence for a Replication Function of Ffa-1, the Xenopus Orthologue of Werner Syndrome Protein Chen, Chin-Yi Graham, Jeanine Yan, Hong J Cell Biol Original Article DNA replication in higher eukaryotic cells occurs at a large number of discrete sites called replication foci. We have previously purified a protein, focus-forming activity 1 (FFA-1), which is involved in the assembly of putative prereplication foci in Xenopus egg extracts. FFA-1 is the orthologue of the Werner syndrome gene product (WRN), a member of the RecQ helicase family. In this paper we show that FFA-1 colocalizes with sites of DNA synthesis and the single-stranded DNA binding protein, replication protein A (RPA), in nuclei reconstituted in the egg extract. In addition, we show that two glutathione S-transferase FFA-1 fusion proteins can inhibit DNA replication in a dominant negative manner. The dominant negative effect correlates with the incorporation of the fusion proteins into replication foci to form “hybrid foci,” which are unable to engage in DNA replication. At the biochemical level, RPA can interact with FFA-1 and specifically stimulates its DNA helicase activity. However, in the presence of the dominant negative mutant proteins, the stimulation is prevented. These results provide the first direct biochemical evidence of an important role for FFA-1 in DNA replication. The Rockefeller University Press 2001-03-05 /pmc/articles/PMC2198806/ /pubmed/11238454 Text en © 2001 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 | Original Article Chen, Chin-Yi Graham, Jeanine Yan, Hong Evidence for a Replication Function of Ffa-1, the Xenopus Orthologue of Werner Syndrome Protein |
title | Evidence for a Replication Function of Ffa-1, the Xenopus Orthologue of Werner Syndrome Protein |
title_full | Evidence for a Replication Function of Ffa-1, the Xenopus Orthologue of Werner Syndrome Protein |
title_fullStr | Evidence for a Replication Function of Ffa-1, the Xenopus Orthologue of Werner Syndrome Protein |
title_full_unstemmed | Evidence for a Replication Function of Ffa-1, the Xenopus Orthologue of Werner Syndrome Protein |
title_short | Evidence for a Replication Function of Ffa-1, the Xenopus Orthologue of Werner Syndrome Protein |
title_sort | evidence for a replication function of ffa-1, the xenopus orthologue of werner syndrome protein |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2198806/ https://www.ncbi.nlm.nih.gov/pubmed/11238454 |
work_keys_str_mv | AT chenchinyi evidenceforareplicationfunctionofffa1thexenopusorthologueofwernersyndromeprotein AT grahamjeanine evidenceforareplicationfunctionofffa1thexenopusorthologueofwernersyndromeprotein AT yanhong evidenceforareplicationfunctionofffa1thexenopusorthologueofwernersyndromeprotein |