ArticleMethods (San Diego, Calif.)2013
A synthetic biology approach to the development of transcriptional regulatory models and custom enhancer design.
Article in Methods (San Diego, Calif.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 15 citations in OpenAlex.
- An in silico analysis of robust but fragile gene regulation links enhancer length to robustness.PLoS computational biology · 2019Article
- Synthetic enhancer design by in silico compensatory evolution reveals flexibility and constraint in cis-regulation.BMC systems biology · 2017Article
- A sequence level model of an intact locus predicts the location and function of nonadditive enhancers.PloS one · 2017Article
- Article
- Parallel Simulated Annealing Using an Adaptive Resampling Interval.Parallel computing · 2016Article
- In silico evolution of the hunchback gene indicates redundancy in cis-regulatory organization and spatial gene expression.Journal of bioinformatics and computational biology · 2014Article
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Authors and funding
4 authors at 1 institution in 1 country.
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Abstract
Synthetic biology offers novel opportunities for elucidating transcriptional regulatory mechanisms and enhancer logic. Complex cis-regulatory sequences--like the ones driving expression of the Drosophila even-skipped gene--have proven difficult to design from existing knowledge, presumably due to the large number of protein-protein interactions needed to drive the correct expression patterns of genes in multicellular organisms. This work discusses two novel computational methods for the custom design of enhancers that employ a sophisticated, empirically validated transcriptional model, optimization algorithms, and synthetic biology. These synthetic elements have both utilitarian and academic value, including improving existing regulatory models as well as evolutionary questions. The first method involves the use of simulated annealing to explore the sequence space for synthetic enhancers whose expression output fit a given search criterion. The second method uses a novel optimization algorithm to find functionally accessible pathways between two enhancer sequences. These paths describe a set of mutations wherein the predicted expression pattern does not significantly vary at any point along the path. Both methods rely on a predictive mathematical framework that maps the enhancer sequence space to functional output.
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Registered trials
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