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Novel features of ARS selection in budding yeast Lachancea kluyveri

BACKGROUND: The characterization of DNA replication origins in yeast has shed much light on the mechanisms of initiation of DNA replication. However, very little is known about the evolution of origins or the evolution of mechanisms through which origins are recognized by the initiation machinery. T...

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Autores principales: Liachko, Ivan, Tanaka, Emi, Cox, Katherine, Chung, Shau Chee Claire, Yang, Lu, Seher, Arael, Hallas, Lindsay, Cha, Eugene, Kang, Gina, Pace, Heather, Barrow, Jasmine, Inada, Maki, Tye, Bik-Kwoon, Keich, Uri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306766/
https://www.ncbi.nlm.nih.gov/pubmed/22204614
http://dx.doi.org/10.1186/1471-2164-12-633
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author Liachko, Ivan
Tanaka, Emi
Cox, Katherine
Chung, Shau Chee Claire
Yang, Lu
Seher, Arael
Hallas, Lindsay
Cha, Eugene
Kang, Gina
Pace, Heather
Barrow, Jasmine
Inada, Maki
Tye, Bik-Kwoon
Keich, Uri
author_facet Liachko, Ivan
Tanaka, Emi
Cox, Katherine
Chung, Shau Chee Claire
Yang, Lu
Seher, Arael
Hallas, Lindsay
Cha, Eugene
Kang, Gina
Pace, Heather
Barrow, Jasmine
Inada, Maki
Tye, Bik-Kwoon
Keich, Uri
author_sort Liachko, Ivan
collection PubMed
description BACKGROUND: The characterization of DNA replication origins in yeast has shed much light on the mechanisms of initiation of DNA replication. However, very little is known about the evolution of origins or the evolution of mechanisms through which origins are recognized by the initiation machinery. This lack of understanding is largely due to the vast evolutionary distances between model organisms in which origins have been examined. RESULTS: In this study we have isolated and characterized autonomously replicating sequences (ARSs) in Lachancea kluyveri - a pre-whole genome duplication (WGD) budding yeast. Through a combination of experimental work and rigorous computational analysis, we show that L. kluyveri ARSs require a sequence that is similar but much longer than the ARS Consensus Sequence well defined in Saccharomyces cerevisiae. Moreover, compared with S. cerevisiae and K. lactis, the replication licensing machinery in L. kluyveri seems more tolerant to variations in the ARS sequence composition. It is able to initiate replication from almost all S. cerevisiae ARSs tested and most Kluyveromyces lactis ARSs. In contrast, only about half of the L. kluyveri ARSs function in S. cerevisiae and less than 10% function in K. lactis. CONCLUSIONS: Our findings demonstrate a replication initiation system with novel features and underscore the functional diversity within the budding yeasts. Furthermore, we have developed new approaches for analyzing biologically functional DNA sequences with ill-defined motifs.
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spelling pubmed-33067662012-03-18 Novel features of ARS selection in budding yeast Lachancea kluyveri Liachko, Ivan Tanaka, Emi Cox, Katherine Chung, Shau Chee Claire Yang, Lu Seher, Arael Hallas, Lindsay Cha, Eugene Kang, Gina Pace, Heather Barrow, Jasmine Inada, Maki Tye, Bik-Kwoon Keich, Uri BMC Genomics Research Article BACKGROUND: The characterization of DNA replication origins in yeast has shed much light on the mechanisms of initiation of DNA replication. However, very little is known about the evolution of origins or the evolution of mechanisms through which origins are recognized by the initiation machinery. This lack of understanding is largely due to the vast evolutionary distances between model organisms in which origins have been examined. RESULTS: In this study we have isolated and characterized autonomously replicating sequences (ARSs) in Lachancea kluyveri - a pre-whole genome duplication (WGD) budding yeast. Through a combination of experimental work and rigorous computational analysis, we show that L. kluyveri ARSs require a sequence that is similar but much longer than the ARS Consensus Sequence well defined in Saccharomyces cerevisiae. Moreover, compared with S. cerevisiae and K. lactis, the replication licensing machinery in L. kluyveri seems more tolerant to variations in the ARS sequence composition. It is able to initiate replication from almost all S. cerevisiae ARSs tested and most Kluyveromyces lactis ARSs. In contrast, only about half of the L. kluyveri ARSs function in S. cerevisiae and less than 10% function in K. lactis. CONCLUSIONS: Our findings demonstrate a replication initiation system with novel features and underscore the functional diversity within the budding yeasts. Furthermore, we have developed new approaches for analyzing biologically functional DNA sequences with ill-defined motifs. BioMed Central 2011-12-28 /pmc/articles/PMC3306766/ /pubmed/22204614 http://dx.doi.org/10.1186/1471-2164-12-633 Text en Copyright ©2011 Liachko et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Liachko, Ivan
Tanaka, Emi
Cox, Katherine
Chung, Shau Chee Claire
Yang, Lu
Seher, Arael
Hallas, Lindsay
Cha, Eugene
Kang, Gina
Pace, Heather
Barrow, Jasmine
Inada, Maki
Tye, Bik-Kwoon
Keich, Uri
Novel features of ARS selection in budding yeast Lachancea kluyveri
title Novel features of ARS selection in budding yeast Lachancea kluyveri
title_full Novel features of ARS selection in budding yeast Lachancea kluyveri
title_fullStr Novel features of ARS selection in budding yeast Lachancea kluyveri
title_full_unstemmed Novel features of ARS selection in budding yeast Lachancea kluyveri
title_short Novel features of ARS selection in budding yeast Lachancea kluyveri
title_sort novel features of ars selection in budding yeast lachancea kluyveri
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306766/
https://www.ncbi.nlm.nih.gov/pubmed/22204614
http://dx.doi.org/10.1186/1471-2164-12-633
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