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Conservation and Variation in Strategies for DNA Replication of Kinetoplastid Nuclear Genomes
INTRODUCTION: Understanding how the nuclear genome of kinetoplastid parasites is replicated received experimental stimulus from sequencing of the Leishmania major, Trypanosoma brucei and Trypanosoma cruzi genomes around 10 years ago. Gene annotations suggested key players in DNA replication initiati...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Bentham Science Publishers
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814967/ https://www.ncbi.nlm.nih.gov/pubmed/29491738 http://dx.doi.org/10.2174/1389202918666170815144627 |
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author | Marques, Catarina A. McCulloch, Richard |
author_facet | Marques, Catarina A. McCulloch, Richard |
author_sort | Marques, Catarina A. |
collection | PubMed |
description | INTRODUCTION: Understanding how the nuclear genome of kinetoplastid parasites is replicated received experimental stimulus from sequencing of the Leishmania major, Trypanosoma brucei and Trypanosoma cruzi genomes around 10 years ago. Gene annotations suggested key players in DNA replication initiation could not be found in these organisms, despite considerable conservation amongst characterised eukaryotes. Initial studies that indicated trypanosomatids might possess an archaeal-like Origin Recognition Complex (ORC), composed of only a single factor termed ORC1/CDC6, have been supplanted by the more recent identification of an ORC in T. brucei. However, the constituent subunits of T. brucei ORC are highly diverged relative to other eukaryotic ORCs and the activity of the complex appears subject to novel, positive regulation. The availability of whole genome sequences has also allowed the deployment of genome-wide strategies to map DNA replication dynamics, to date in T. brucei and Leishmania. ORC1/CDC6 binding and function in T. brucei displays pronounced overlap with the unconventional organisation of gene expression in the genome. Moreover, mapping of sites of replication initiation suggests pronounced differences in replication dynamics in Leishmania relative to T. brucei. CONCLUSION: Here we discuss what implications these emerging data may have for parasite and eukaryotic biology of DNA replication. |
format | Online Article Text |
id | pubmed-5814967 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Bentham Science Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-58149672018-08-01 Conservation and Variation in Strategies for DNA Replication of Kinetoplastid Nuclear Genomes Marques, Catarina A. McCulloch, Richard Curr Genomics Article INTRODUCTION: Understanding how the nuclear genome of kinetoplastid parasites is replicated received experimental stimulus from sequencing of the Leishmania major, Trypanosoma brucei and Trypanosoma cruzi genomes around 10 years ago. Gene annotations suggested key players in DNA replication initiation could not be found in these organisms, despite considerable conservation amongst characterised eukaryotes. Initial studies that indicated trypanosomatids might possess an archaeal-like Origin Recognition Complex (ORC), composed of only a single factor termed ORC1/CDC6, have been supplanted by the more recent identification of an ORC in T. brucei. However, the constituent subunits of T. brucei ORC are highly diverged relative to other eukaryotic ORCs and the activity of the complex appears subject to novel, positive regulation. The availability of whole genome sequences has also allowed the deployment of genome-wide strategies to map DNA replication dynamics, to date in T. brucei and Leishmania. ORC1/CDC6 binding and function in T. brucei displays pronounced overlap with the unconventional organisation of gene expression in the genome. Moreover, mapping of sites of replication initiation suggests pronounced differences in replication dynamics in Leishmania relative to T. brucei. CONCLUSION: Here we discuss what implications these emerging data may have for parasite and eukaryotic biology of DNA replication. Bentham Science Publishers 2018-02 2018-02 /pmc/articles/PMC5814967/ /pubmed/29491738 http://dx.doi.org/10.2174/1389202918666170815144627 Text en © 2018 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Marques, Catarina A. McCulloch, Richard Conservation and Variation in Strategies for DNA Replication of Kinetoplastid Nuclear Genomes |
title | Conservation and Variation in Strategies for DNA Replication of Kinetoplastid Nuclear Genomes |
title_full | Conservation and Variation in Strategies for DNA Replication of Kinetoplastid Nuclear Genomes |
title_fullStr | Conservation and Variation in Strategies for DNA Replication of Kinetoplastid Nuclear Genomes |
title_full_unstemmed | Conservation and Variation in Strategies for DNA Replication of Kinetoplastid Nuclear Genomes |
title_short | Conservation and Variation in Strategies for DNA Replication of Kinetoplastid Nuclear Genomes |
title_sort | conservation and variation in strategies for dna replication of kinetoplastid nuclear genomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814967/ https://www.ncbi.nlm.nih.gov/pubmed/29491738 http://dx.doi.org/10.2174/1389202918666170815144627 |
work_keys_str_mv | AT marquescatarinaa conservationandvariationinstrategiesfordnareplicationofkinetoplastidnucleargenomes AT mccullochrichard conservationandvariationinstrategiesfordnareplicationofkinetoplastidnucleargenomes |