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Biology subjects

Javier Estrada

Publications and source records attributed to Javier Estrada.

2 recordsLinked to original sources

SiteOut: an online tool to design binding site-free DNA sequences

DNA-binding proteins control many fundamental biological processes such as transcription, recombination and replication. A major goal is to decipher the role that DNA sequence plays in orchestrating the binding and activity of such regulatory proteins. To address this goal, it is useful to rationally design DNA sequences with desired numbers, affinities and arrangements of protein binding sites. However, removing binding sites from DNA is computationally non-trivial since one risks creating new sites in the process of deleting or moving others. Here we present an online binding site removal tool, SiteOut, that enables users to design arbitrary DNA sequences that entirely lack binding sites for factors of interest. SiteOut can also be used to delete sites from a specific sequence, or to introduce site-free spacers between functional sequences without creating new sites at the junctions. In combination with commercial DNA synthesis services, SiteOut provides a powerful and flexible platform for synthetic projects that interrogate regulatory DNA. Here we describe the algorithm and illustrate the ways in which SiteOut can be used; it is publicly available at https://depace.med.harvard.edu/siteout/.

Genetics

Shadow enhancers enable Hunchback bifunctionality in the Drosophila embryo

Hunchback (Hb) is a bifunctional transcription factor that activates and represses distinct enhancers. Here, we investigate the hypothesis that Hb can activate and repress the same enhancer. Computational models predicted that Hb bifunctionally regulates the even-skipped (eve) stripe 3+7 enhancer (eve3+7) in Drosophila blastoderm embryos. We measured and modeled eve expression at cellular resolution under multiple genetic perturbations and found that the eve3+7 enhancer could not explain endogenous eve stripe 7 behavior. Instead, we found that eve stripe 7 is controlled by two enhancers: the canonical eve3+7 and a sequence encompassing the minimal eve stripe 2 enhancer (eve2+7). Hb bifunctionally regulates eve stripe 7, but it executes these two activities on different pieces of regulatory DNA-it activates the eve2+7 enhancer and represses the eve3+7 enhancer. These two \"shadow enhancers\" use different regulatory logic to create the same pattern.\n\nSignificance statementEnhancers are regions of regulatory DNA that control gene expression and cell fate decisions during development. Enhancers compute the expression pattern of their target gene by reading the concentrations of input regulatory proteins. Many developmental genes contain multiple enhancers that control the same output pattern, but it is unclear if these enhancers all compute the pattern in the same way. We use measurements in single cells and computational models in Drosophila embryos to demonstrate that two enhancers that encode the same gene expression pattern compute differently: the same regulatory protein represses one enhancer and activates the other. Pairs of enhancers that output the same pattern by performing different computations may impart special properties to developmental systems.

Systems Biology