↓ Skip to main content

PLOS

Mutual Repression Enhances the Steepness and Precision of Gene Expression Boundaries

Overview of attention for article published in PLoS Computational Biology, August 2012
Altmetric Badge

Mentioned by

facebook
1 Facebook page

Readers on

mendeley
76 Mendeley
citeulike
1 CiteULike
Title
Mutual Repression Enhances the Steepness and Precision of Gene Expression Boundaries
Published in
PLoS Computational Biology, August 2012
DOI 10.1371/journal.pcbi.1002654
Pubmed ID
Authors

Thomas R. Sokolowski, Thorsten Erdmann, Pieter Rein ten Wolde

Abstract

Embryonic development is driven by spatial patterns of gene expression that determine the fate of each cell in the embryo. While gene expression is often highly erratic, embryonic development is usually exceedingly precise. In particular, gene expression boundaries are robust not only against intra-embryonic fluctuations such as noise in gene expression and protein diffusion, but also against embryo-to-embryo variations in the morphogen gradients, which provide positional information to the differentiating cells. How development is robust against intra- and inter-embryonic variations is not understood. A common motif in the gene regulation networks that control embryonic development is mutual repression between pairs of genes. To assess the role of mutual repression in the robust formation of gene expression patterns, we have performed large-scale stochastic simulations of a minimal model of two mutually repressing gap genes in Drosophila, hunchback (hb) and knirps (kni). Our model includes not only mutual repression between hb and kni, but also the stochastic and cooperative activation of hb by the anterior morphogen Bicoid (Bcd) and of kni by the posterior morphogen Caudal (Cad), as well as the diffusion of Hb and Kni between neighboring nuclei. Our analysis reveals that mutual repression can markedly increase the steepness and precision of the gap gene expression boundaries. In contrast to other mechanisms such as spatial averaging and cooperative gene activation, mutual repression thus allows for gene-expression boundaries that are both steep and precise. Moreover, mutual repression dramatically enhances their robustness against embryo-to-embryo variations in the morphogen levels. Finally, our simulations reveal that diffusion of the gap proteins plays a critical role not only in reducing the width of the gap gene expression boundaries via the mechanism of spatial averaging, but also in repairing patterning errors that could arise because of the bistability induced by mutual repression.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 76 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 4 5%
United Kingdom 1 1%
Argentina 1 1%
Austria 1 1%
Unknown 69 91%

Demographic breakdown

Readers by professional status Count As %
Researcher 25 33%
Student > Ph. D. Student 14 18%
Student > Master 6 8%
Student > Doctoral Student 5 7%
Professor 4 5%
Other 13 17%
Unknown 9 12%
Readers by discipline Count As %
Agricultural and Biological Sciences 33 43%
Biochemistry, Genetics and Molecular Biology 11 14%
Physics and Astronomy 9 12%
Mathematics 3 4%
Unspecified 2 3%
Other 7 9%
Unknown 11 14%