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Modeling the Hes1 oscillator.
J. Comput. Biol. 14, 984-1000 (2007)
Somitogenesis describes the segmentation of vertebrate embryonic bodies, which is thought to be induced by ultradian clocks (i.e., clocks with relatively short cycles compared to circadian clocks). One candidate for such a clock is the bHLH factor Hes1, forming dimers which repress the transcription of its own encoding gene. Most models for such small autoregulative networks are based on delay equations where a Hill function represents the regulation of transcription. The aim of the present paper is to estimate the Hill coefficient in the switch of an Hes1 oscillator and to suggest a more detailed model of the autoregulative network. The promoter of Hes1 consists of three to four binding sites for Hes1 dimers. Using the sparse data from literature, we find, in contrast to other statements in literature, that there is not much evidence for synergistic binding in the regulatory region of Hes1, and that the Hill coefficient is about three. As a model for the negative feedback loop, we use a Goodwin system and find sustained oscillations for systems with a large enough number of linear differential equations. By a suitable variation of the number of equations, we provide a rational lower bound for the Hill coefficient for such a system. Our results suggest that there exist additional nonlinear processes outside of the regulatory region of Hes1.
Impact Factor
Scopus SNIP
Web of Science
Times Cited
Times Cited
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Cited By
Cited By
Altmetric
2.000
0.000
40
42
Anmerkungen
Besondere Publikation
Auf Hompepage verbergern
Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
computational molecular biology; gene expressions; Hes1; oscillations; negative feedback loop; regulatory regions; Hill coefficient
Sprache
Veröffentlichungsjahr
2007
HGF-Berichtsjahr
2007
ISSN (print) / ISBN
1066-5277
e-ISSN
1557-8666
Zeitschrift
Journal of Computational Biology
Quellenangaben
Band: 14,
Heft: 7,
Seiten: 984-1000
Verlag
Mary Ann Liebert
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Biomathematics and Biometry (IBB)
PSP-Element(e)
FE 73821
WOS ID
000249521700008
Scopus ID
34548742372
PubMed ID
17803375
Erfassungsdatum
2007-12-31