Role of DNA binding sites and slow unbinding kinetics in titration-based oscillators.

dc.contributor.author

Karapetyan, Sargis

dc.contributor.author

Buchler, Nicolas E

dc.coverage.spatial

United States

dc.date.accessioned

2016-01-11T23:41:38Z

dc.date.issued

2015-12

dc.description.abstract

Genetic oscillators, such as circadian clocks, are constantly perturbed by molecular noise arising from the small number of molecules involved in gene regulation. One of the strongest sources of stochasticity is the binary noise that arises from the binding of a regulatory protein to a promoter in the chromosomal DNA. In this study, we focus on two minimal oscillators based on activator titration and repressor titration to understand the key parameters that are important for oscillations and for overcoming binary noise. We show that the rate of unbinding from the DNA, despite traditionally being considered a fast parameter, needs to be slow to broaden the space of oscillatory solutions. The addition of multiple, independent DNA binding sites further expands the oscillatory parameter space for the repressor-titration oscillator and lengthens the period of both oscillators. This effect is a combination of increased effective delay of the unbinding kinetics due to multiple binding sites and increased promoter ultrasensitivity that is specific for repression. We then use stochastic simulation to show that multiple binding sites increase the coherence of oscillations by mitigating the binary noise. Slow values of DNA unbinding rate are also effective in alleviating molecular noise due to the increased distance from the bifurcation point. Our work demonstrates how the number of DNA binding sites and slow unbinding kinetics, which are often omitted in biophysical models of gene circuits, can have a significant impact on the temporal and stochastic dynamics of genetic oscillators.

dc.identifier

http://www.ncbi.nlm.nih.gov/pubmed/26764732

dc.identifier.eissn

1550-2376

dc.identifier.uri

https://hdl.handle.net/10161/11506

dc.language

eng

dc.publisher

American Physical Society (APS)

dc.relation.ispartof

Phys Rev E Stat Nonlin Soft Matter Phys

dc.relation.isversionof

10.1103/PhysRevE.92.062712

dc.subject

Binding Sites

dc.subject

Circadian Clocks

dc.subject

DNA

dc.subject

Kinetics

dc.subject

Models, Genetic

dc.subject

Stochastic Processes

dc.title

Role of DNA binding sites and slow unbinding kinetics in titration-based oscillators.

dc.type

Journal article

duke.contributor.orcid

Buchler, Nicolas E|0000-0003-3940-3432

pubs.author-url

http://www.ncbi.nlm.nih.gov/pubmed/26764732

pubs.begin-page

062712

pubs.issue

6

pubs.organisational-group

Biology

pubs.organisational-group

Duke

pubs.organisational-group

Physics

pubs.organisational-group

Trinity College of Arts & Sciences

pubs.publication-status

Published

pubs.volume

92

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Phys. Rev. E 2015 Karapetyan.pdf
Size:
1.28 MB
Format:
Adobe Portable Document Format
Description:
Published version