Literature DB >> 26779176

Editorial: DNA Replication Origins in Microbial Genomes.

Feng Gao1.   

Abstract

Entities:  

Keywords:  DNA replication; archaea; bacteria; orisome; regulatory proteins; replication origin; replication regulation; yeast

Year:  2016        PMID: 26779176      PMCID: PMC4705448          DOI: 10.3389/fmicb.2015.01545

Source DB:  PubMed          Journal:  Front Microbiol        ISSN: 1664-302X            Impact factor:   5.640


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In all three domains of life, DNA replication initiates on defined genome sites, termed replication origins. In bacteria, replication typically initiates from a single replication origin (oriC). In eukaryotic genomes, replication initiates from significantly more replication origins, ranging from hundreds in yeast to tens of thousands in human (Gao et al., 2012). Within the archaeal domain, multiple replication origins have been identified in Sulfolobus species, haloarchaea etc. (Lundgren et al., 2004; Robinson et al., 2004; Wu et al.; Yang et al., 2015). The research on replication origins is important not only in providing insights into the structure and function of the replication origins but also in understanding the regulatory mechanisms of the initiation step in DNA replication. Therefore, intensive studies, by in silico analyses as well as in vivo and in vitro experiments, have been carried out in the last two decades. Based on the sequence-derived features, various in silico approaches have been developed to identify microbial replication origins (Frank and Lobry, 2000; Breier et al., 2004; Mackiewicz et al., 2004; Zhang and Zhang, 2005; Worning et al., 2006; Gao and Zhang, 2007, 2008a; Gao et al., 2013; Gao, 2014). For example, the locations of replication origins sites have been predicted for thousands of bacterial genomes by Ori-Finder, a web-based system for finding oriCs in bacterial genomes (Gao and Zhang, 2007; Gao et al., 2013). A new version of Ori-Finder for archaea, Ori-Finder 2, has been developed to predict oriCs in archaeal genomes automatically (Luo et al.). To confirm the predicted replication origins, it is important to choose a most suitable experimental strategy. Song et al. summarize the main existing experimental methods to determine the replication origin regions and their practical applications (Song et al.). As a study from in silico to in vitro, the experimental supports are provided for the identified replication origins in Cyanothece ATCC 51142 (Gao and Zhang, 2008b), and their interactions with the initiator protein DnaA (Huang et al.). In spite of a great variety of origin sequences across species, all bacterial replication origins contain the information necessary to guide assembly of the DnaA protein complex at oriC, triggering the unwinding of DNA and the beginning of replication. Therefore, oriC-encoded instructions should be interpreted particularly in the context of replication initiation and its regulation (Wolanski et al.). Wolanski et al. show that oriC-encoded instructions allow not only for initiation but also for precise regulation of replication initiation and coordination of chromosomal replication with the cell cycle (also in response to environmental signals; Wolanski et al.). Frimodt-Moller et al. find control regions for chromosome replication are conserved with respect to sequence and location among Escherichia coli strains (Frimodt-Moller et al.). Based on the single origin usage strategy that distinguishes bacteria, Marczynski et al. redefine the bacterial origins as centralized information processors, and describe how negative-feedback, phospho-relay, and chromosome-partitioning systems act to regulate chromosome replication (Marczynski et al.). On the other hand, the in silico analyses show that some bacteria, although very few, may have multiple origins of replication per chromosome (Frank et al., 2015; Gao), and the recent work also suggests that there are multiple replication origins in Synechocystis that fire asynchronously, as in eukaryotic nuclear chromosomal replication (Ohbayashi et al., 2015). For eukaryotic organisms, replication origins are best characterized in the unicellular eukaryote budding yeast Saccharomyces cerevisiae and the fission yeast Schizosaccharomyces pombe. With the recent development of genome-wide approaches, the number of yeast species involved in ORIs research has increased dramatically, which has created opportunities for the sequence, protein, and comparative analysis of replication origins in yeast genomes (Li et al.; Zheng et al.; Peng et al.). The Frontiers in Microbiology Research Topic on DNA replication origins in microbial genomes is devoted to address the issues mentioned above, and aims to provide a comprehensive overview of the current research in this field.

Dedication

This article is dedicated to the 120th Anniversary of Tianjin University (formerly Peiyang University), the first modern higher education university in China.

Conflict of interest statement

The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
  16 in total

1.  Oriloc: prediction of replication boundaries in unannotated bacterial chromosomes.

Authors:  A C Frank; J R Lobry
Journal:  Bioinformatics       Date:  2000-06       Impact factor: 6.937

2.  Identification of two origins of replication in the single chromosome of the archaeon Sulfolobus solfataricus.

Authors:  Nicholas P Robinson; Isabelle Dionne; Magnus Lundgren; Victoria L Marsh; Rolf Bernander; Stephen D Bell
Journal:  Cell       Date:  2004-01-09       Impact factor: 41.582

3.  Where does bacterial replication start? Rules for predicting the oriC region.

Authors:  Pawel Mackiewicz; Jolanta Zakrzewska-Czerwinska; Anna Zawilak; Miroslaw R Dudek; Stanislaw Cebrat
Journal:  Nucleic Acids Res       Date:  2004-07-16       Impact factor: 16.971

Review 4.  Identification of replication origins in archaeal genomes based on the Z-curve method.

Authors:  Ren Zhang; Chun-Ting Zhang
Journal:  Archaea       Date:  2005-05       Impact factor: 3.273

5.  Origins of replication in Cyanothece 51142.

Authors:  Feng Gao; Chun-Ting Zhang
Journal:  Proc Natl Acad Sci U S A       Date:  2008-12-30       Impact factor: 11.205

6.  Ocean's Twelve: flagellar and biofilm chromids in the multipartite genome of Marinovum algicola DG898 exemplify functional compartmentalization.

Authors:  Oliver Frank; Markus Göker; Silke Pradella; Jörn Petersen
Journal:  Environ Microbiol       Date:  2015-09-10       Impact factor: 5.491

7.  Three replication origins in Sulfolobus species: synchronous initiation of chromosome replication and asynchronous termination.

Authors:  Magnus Lundgren; Anders Andersson; Lanming Chen; Peter Nilsson; Rolf Bernander
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-23       Impact factor: 11.205

8.  DoriC 5.0: an updated database of oriC regions in both bacterial and archaeal genomes.

Authors:  Feng Gao; Hao Luo; Chun-Ting Zhang
Journal:  Nucleic Acids Res       Date:  2012-10-23       Impact factor: 16.971

9.  Prediction of Saccharomyces cerevisiae replication origins.

Authors:  Adam M Breier; Sourav Chatterji; Nicholas R Cozzarelli
Journal:  Genome Biol       Date:  2004-03-04       Impact factor: 13.583

10.  Recent Advances in the Identification of Replication Origins Based on the Z-curve Method.

Authors:  Feng Gao
Journal:  Curr Genomics       Date:  2014-04       Impact factor: 2.236

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  1 in total

1.  Editorial: DNA Replication Origins in Microbial Genomes, Volume 2.

Authors:  Feng Gao; Alan C Leonard
Journal:  Front Microbiol       Date:  2019-10-23       Impact factor: 5.640

  1 in total

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