Evolution of cell cycle control: same molecular machines, different regulation

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Standard

Evolution of cell cycle control : same molecular machines, different regulation. / de Lichtenberg, Ulrik; Jensen, Thomas Skøt; Brunak, Søren; Bork, Peer; Jensen, Lars Juhl.

In: Cell Cycle, Vol. 6, No. 15, 2007, p. 1819-25.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

de Lichtenberg, U, Jensen, TS, Brunak, S, Bork, P & Jensen, LJ 2007, 'Evolution of cell cycle control: same molecular machines, different regulation', Cell Cycle, vol. 6, no. 15, pp. 1819-25.

APA

de Lichtenberg, U., Jensen, T. S., Brunak, S., Bork, P., & Jensen, L. J. (2007). Evolution of cell cycle control: same molecular machines, different regulation. Cell Cycle, 6(15), 1819-25.

Vancouver

de Lichtenberg U, Jensen TS, Brunak S, Bork P, Jensen LJ. Evolution of cell cycle control: same molecular machines, different regulation. Cell Cycle. 2007;6(15):1819-25.

Author

de Lichtenberg, Ulrik ; Jensen, Thomas Skøt ; Brunak, Søren ; Bork, Peer ; Jensen, Lars Juhl. / Evolution of cell cycle control : same molecular machines, different regulation. In: Cell Cycle. 2007 ; Vol. 6, No. 15. pp. 1819-25.

Bibtex

@article{f1fb0805d07a4fe9af09448ccffdd775,
title = "Evolution of cell cycle control: same molecular machines, different regulation",
abstract = "Decades of research has together with the availability of whole genomes made it clear that many of the core components involved in the cell cycle are conserved across eukaryotes, both functionally and structurally. These proteins are organized in complexes and modules that are activated or deactivated at specific stages during the cell cycle through a wide variety of mechanisms including transcriptional regulation, phosphorylation, subcellular translocation and targeted degradation. In a series of integrative analyses of different genome-scale data sets, we have studied how these different layers of regulation together control the activity of cell cycle complexes and how this regulation has evolved. The results show surprisingly poor conservation of both the transcriptional and the post-translation regulation of individual genes and proteins; however, the changes in one layer of regulation are often mirrored by changes in other layers, implying that independent layers of control coevolve. By taking a bird's eye view of the cell cycle, we demonstrate how the modular organization of cellular systems possesses a built-in flexibility, which allows evolution to find many different solutions for assembling the same molecular machines just in time for action.",
author = "{de Lichtenberg}, Ulrik and Jensen, {Thomas Sk{\o}t} and S{\o}ren Brunak and Peer Bork and Jensen, {Lars Juhl}",
year = "2007",
language = "English",
volume = "6",
pages = "1819--25",
journal = "Cell Cycle",
issn = "1538-4101",
publisher = "Taylor & Francis",
number = "15",

}

RIS

TY - JOUR

T1 - Evolution of cell cycle control

T2 - same molecular machines, different regulation

AU - de Lichtenberg, Ulrik

AU - Jensen, Thomas Skøt

AU - Brunak, Søren

AU - Bork, Peer

AU - Jensen, Lars Juhl

PY - 2007

Y1 - 2007

N2 - Decades of research has together with the availability of whole genomes made it clear that many of the core components involved in the cell cycle are conserved across eukaryotes, both functionally and structurally. These proteins are organized in complexes and modules that are activated or deactivated at specific stages during the cell cycle through a wide variety of mechanisms including transcriptional regulation, phosphorylation, subcellular translocation and targeted degradation. In a series of integrative analyses of different genome-scale data sets, we have studied how these different layers of regulation together control the activity of cell cycle complexes and how this regulation has evolved. The results show surprisingly poor conservation of both the transcriptional and the post-translation regulation of individual genes and proteins; however, the changes in one layer of regulation are often mirrored by changes in other layers, implying that independent layers of control coevolve. By taking a bird's eye view of the cell cycle, we demonstrate how the modular organization of cellular systems possesses a built-in flexibility, which allows evolution to find many different solutions for assembling the same molecular machines just in time for action.

AB - Decades of research has together with the availability of whole genomes made it clear that many of the core components involved in the cell cycle are conserved across eukaryotes, both functionally and structurally. These proteins are organized in complexes and modules that are activated or deactivated at specific stages during the cell cycle through a wide variety of mechanisms including transcriptional regulation, phosphorylation, subcellular translocation and targeted degradation. In a series of integrative analyses of different genome-scale data sets, we have studied how these different layers of regulation together control the activity of cell cycle complexes and how this regulation has evolved. The results show surprisingly poor conservation of both the transcriptional and the post-translation regulation of individual genes and proteins; however, the changes in one layer of regulation are often mirrored by changes in other layers, implying that independent layers of control coevolve. By taking a bird's eye view of the cell cycle, we demonstrate how the modular organization of cellular systems possesses a built-in flexibility, which allows evolution to find many different solutions for assembling the same molecular machines just in time for action.

M3 - Journal article

VL - 6

SP - 1819

EP - 1825

JO - Cell Cycle

JF - Cell Cycle

SN - 1538-4101

IS - 15

ER -

ID: 46461049