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Identification of ORC1/CDC6-Interacting Factors in Trypanosoma brucei Reveals Critical Features of Origin Recognition Complex Architecture

DNA Replication initiates by formation of a pre-replication complex on sequences termed origins. In eukaryotes, the pre-replication complex is composed of the Origin Recognition Complex (ORC), Cdc6 and the MCM replicative helicase in conjunction with Cdt1. Eukaryotic ORC is considered to be composed...

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Autores principales: Tiengwe, Calvin, Marcello, Lucio, Farr, Helen, Gadelha, Catarina, Burchmore, Richard, Barry, J. David, Bell, Stephen D., McCulloch, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297607/
https://www.ncbi.nlm.nih.gov/pubmed/22412905
http://dx.doi.org/10.1371/journal.pone.0032674
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author Tiengwe, Calvin
Marcello, Lucio
Farr, Helen
Gadelha, Catarina
Burchmore, Richard
Barry, J. David
Bell, Stephen D.
McCulloch, Richard
author_facet Tiengwe, Calvin
Marcello, Lucio
Farr, Helen
Gadelha, Catarina
Burchmore, Richard
Barry, J. David
Bell, Stephen D.
McCulloch, Richard
author_sort Tiengwe, Calvin
collection PubMed
description DNA Replication initiates by formation of a pre-replication complex on sequences termed origins. In eukaryotes, the pre-replication complex is composed of the Origin Recognition Complex (ORC), Cdc6 and the MCM replicative helicase in conjunction with Cdt1. Eukaryotic ORC is considered to be composed of six subunits, named Orc1–6, and monomeric Cdc6 is closely related in sequence to Orc1. However, ORC has been little explored in protists, and only a single ORC protein, related to both Orc1 and Cdc6, has been shown to act in DNA replication in Trypanosoma brucei. Here we identify three highly diverged putative T. brucei ORC components that interact with ORC1/CDC6 and contribute to cell division. Two of these factors are so diverged that we cannot determine if they are eukaryotic ORC subunit orthologues, or are parasite-specific replication factors. The other we show to be a highly diverged Orc4 orthologue, demonstrating that this is one of the most widely conserved ORC subunits in protists and revealing it to be a key element of eukaryotic ORC architecture. Additionally, we have examined interactions amongst the T. brucei MCM subunits and show that this has the conventional eukaryotic heterohexameric structure, suggesting that divergence in the T. brucei replication machinery is limited to the earliest steps in origin licensing.
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spelling pubmed-32976072012-03-12 Identification of ORC1/CDC6-Interacting Factors in Trypanosoma brucei Reveals Critical Features of Origin Recognition Complex Architecture Tiengwe, Calvin Marcello, Lucio Farr, Helen Gadelha, Catarina Burchmore, Richard Barry, J. David Bell, Stephen D. McCulloch, Richard PLoS One Research Article DNA Replication initiates by formation of a pre-replication complex on sequences termed origins. In eukaryotes, the pre-replication complex is composed of the Origin Recognition Complex (ORC), Cdc6 and the MCM replicative helicase in conjunction with Cdt1. Eukaryotic ORC is considered to be composed of six subunits, named Orc1–6, and monomeric Cdc6 is closely related in sequence to Orc1. However, ORC has been little explored in protists, and only a single ORC protein, related to both Orc1 and Cdc6, has been shown to act in DNA replication in Trypanosoma brucei. Here we identify three highly diverged putative T. brucei ORC components that interact with ORC1/CDC6 and contribute to cell division. Two of these factors are so diverged that we cannot determine if they are eukaryotic ORC subunit orthologues, or are parasite-specific replication factors. The other we show to be a highly diverged Orc4 orthologue, demonstrating that this is one of the most widely conserved ORC subunits in protists and revealing it to be a key element of eukaryotic ORC architecture. Additionally, we have examined interactions amongst the T. brucei MCM subunits and show that this has the conventional eukaryotic heterohexameric structure, suggesting that divergence in the T. brucei replication machinery is limited to the earliest steps in origin licensing. Public Library of Science 2012-03-08 /pmc/articles/PMC3297607/ /pubmed/22412905 http://dx.doi.org/10.1371/journal.pone.0032674 Text en Tiengwe et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Tiengwe, Calvin
Marcello, Lucio
Farr, Helen
Gadelha, Catarina
Burchmore, Richard
Barry, J. David
Bell, Stephen D.
McCulloch, Richard
Identification of ORC1/CDC6-Interacting Factors in Trypanosoma brucei Reveals Critical Features of Origin Recognition Complex Architecture
title Identification of ORC1/CDC6-Interacting Factors in Trypanosoma brucei Reveals Critical Features of Origin Recognition Complex Architecture
title_full Identification of ORC1/CDC6-Interacting Factors in Trypanosoma brucei Reveals Critical Features of Origin Recognition Complex Architecture
title_fullStr Identification of ORC1/CDC6-Interacting Factors in Trypanosoma brucei Reveals Critical Features of Origin Recognition Complex Architecture
title_full_unstemmed Identification of ORC1/CDC6-Interacting Factors in Trypanosoma brucei Reveals Critical Features of Origin Recognition Complex Architecture
title_short Identification of ORC1/CDC6-Interacting Factors in Trypanosoma brucei Reveals Critical Features of Origin Recognition Complex Architecture
title_sort identification of orc1/cdc6-interacting factors in trypanosoma brucei reveals critical features of origin recognition complex architecture
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297607/
https://www.ncbi.nlm.nih.gov/pubmed/22412905
http://dx.doi.org/10.1371/journal.pone.0032674
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