↓ Skip to main content

PLOS

Efficient Reverse-Engineering of a Developmental Gene Regulatory Network

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

Mentioned by

twitter
7 X users

Citations

dimensions_citation
86 Dimensions

Readers on

mendeley
125 Mendeley
citeulike
2 CiteULike
Title
Efficient Reverse-Engineering of a Developmental Gene Regulatory Network
Published in
PLoS Computational Biology, July 2012
DOI 10.1371/journal.pcbi.1002589
Pubmed ID
Authors

Anton Crombach, Karl R. Wotton, Damjan Cicin-Sain, Maksat Ashyraliyev, Johannes Jaeger

Abstract

Understanding the complex regulatory networks underlying development and evolution of multi-cellular organisms is a major problem in biology. Computational models can be used as tools to extract the regulatory structure and dynamics of such networks from gene expression data. This approach is called reverse engineering. It has been successfully applied to many gene networks in various biological systems. However, to reconstitute the structure and non-linear dynamics of a developmental gene network in its spatial context remains a considerable challenge. Here, we address this challenge using a case study: the gap gene network involved in segment determination during early development of Drosophila melanogaster. A major problem for reverse-engineering pattern-forming networks is the significant amount of time and effort required to acquire and quantify spatial gene expression data. We have developed a simplified data processing pipeline that considerably increases the throughput of the method, but results in data of reduced accuracy compared to those previously used for gap gene network inference. We demonstrate that we can infer the correct network structure using our reduced data set, and investigate minimal data requirements for successful reverse engineering. Our results show that timing and position of expression domain boundaries are the crucial features for determining regulatory network structure from data, while it is less important to precisely measure expression levels. Based on this, we define minimal data requirements for gap gene network inference. Our results demonstrate the feasibility of reverse-engineering with much reduced experimental effort. This enables more widespread use of the method in different developmental contexts and organisms. Such systematic application of data-driven models to real-world networks has enormous potential. Only the quantitative investigation of a large number of developmental gene regulatory networks will allow us to discover whether there are rules or regularities governing development and evolution of complex multi-cellular organisms.

X Demographics

X Demographics

The data shown below were collected from the profiles of 7 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 125 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 4 3%
France 3 2%
India 2 2%
Brazil 1 <1%
Spain 1 <1%
United Kingdom 1 <1%
Unknown 113 90%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 41 33%
Researcher 35 28%
Student > Master 11 9%
Student > Bachelor 9 7%
Professor 8 6%
Other 14 11%
Unknown 7 6%
Readers by discipline Count As %
Agricultural and Biological Sciences 64 51%
Biochemistry, Genetics and Molecular Biology 19 15%
Computer Science 9 7%
Physics and Astronomy 5 4%
Engineering 5 4%
Other 14 11%
Unknown 9 7%