DNA Replication Control in Microbial Cell Factories / by Monika Glinkowska, Lidia Boss, Grzegorz Wegrzyn
By: Glinkowska, Monika
Contributor(s): Boss, Lidia
| Wegrzyn, Grzegorz.
Material type:
E-bookSeries: SpringerBriefs in MicrobiologyPublisher: Cham, Switzerland : Springer, 2015Description: 1 recurso en línea (V, 50 p.) 4 il. col..ISBN: 9783319105338.Subject: ADN -- Replicación
Summary: This work describes the current knowledge of biochemical mechanisms regulating initiation of DNA replication in Escherichia coli, which focuses on the control ofÂ{u0863}tivity of the DnaA protein. Examples of direct linkages between DNA replication and other cellular processes are provided. In addition,Â{u3A6D}ilarities of the mechanisms of regulation of DNA replication operating in prokaryotic and eukaryotic cells are identified, andÂ{u9B70}lications for understanding more complex processes, like carcinogenesis are suggested. Studies of recent years provided evidence that regulation of DNA replication in bacteria is more complex than previously anticipated. Multiple layers of control seem to ensure coordination of this process with the increase of cellular mass and the division cycle. Metabolic processes and membrane composition may serve as points where integration of genome replication with growth conditions occurs. It is also likely that coupling ofÂĎA synthesis with cellular metabolism may involve interactions of replication proteins with other macromolecular complexes, responsible for various cellular processes. Thus, the exact set of factors participating in triggering the replication initiation may differ depending on growth conditions. Therefore, understanding the regulation of DNA duplication requires placing this process in the context ofÂ{u4A25} current knowledge on bacterial metabolism, as well as cellular and chromosomal structure. Moreover, in both Escherichia coli and eukaryotic cells, replication initiator proteins were shown to play other roles in addition to driving the assembly of replication complexes, which constitutes another, yet not sufficiently understood, layer of coordinating DNA replication with the cell cycle.
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Madrid Digital Acceso Electrónico (UEM) | Ciencias de la Salud | QP624.5.R48 G556 2015 EB (Browse shelf(Opens below)) | .i11568252 | Acceso electrónico | eBOOK .i11568252 |
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This work describes the current knowledge of biochemical mechanisms regulating initiation of DNA replication in Escherichia coli, which focuses on the control ofÂ{u0863}tivity of the DnaA protein. Examples of direct linkages between DNA replication and other cellular processes are provided. In addition,Â{u3A6D}ilarities of the mechanisms of regulation of DNA replication operating in prokaryotic and eukaryotic cells are identified, andÂ{u9B70}lications for understanding more complex processes, like carcinogenesis are suggested. Studies of recent years provided evidence that regulation of DNA replication in bacteria is more complex than previously anticipated. Multiple layers of control seem to ensure coordination of this process with the increase of cellular mass and the division cycle. Metabolic processes and membrane composition may serve as points where integration of genome replication with growth conditions occurs. It is also likely that coupling ofÂĎA synthesis with cellular metabolism may involve interactions of replication proteins with other macromolecular complexes, responsible for various cellular processes. Thus, the exact set of factors participating in triggering the replication initiation may differ depending on growth conditions. Therefore, understanding the regulation of DNA duplication requires placing this process in the context ofÂ{u4A25} current knowledge on bacterial metabolism, as well as cellular and chromosomal structure. Moreover, in both Escherichia coli and eukaryotic cells, replication initiator proteins were shown to play other roles in addition to driving the assembly of replication complexes, which constitutes another, yet not sufficiently understood, layer of coordinating DNA replication with the cell cycle.
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