Format

Send to

Choose Destination
PLoS One. 2019 Jan 7;14(1):e0209349. doi: 10.1371/journal.pone.0209349. eCollection 2019.

Analysis of the transcriptional logic governing differential spatial expression in Hh target genes.

Author information

1
Applied Mathematics Department, University of Granada, Granada, Spain.
2
Excellence Research Unit "Modeling Nature" (MNat), University of Granada, Granada, Spain.

Abstract

This work provides theoretical tools to analyse the transcriptional effects of certain biochemical mechanisms (i.e. affinity and cooperativity) that have been proposed in previous literature to explain the proper spatial expression of Hedgehog target genes involved in Drosophila development. Specifically we have focused on the expression of decapentaplegic, wingless, stripe and patched. The transcription of these genes is believed to be controlled by enhancer modules able to interpret opposing gradients of the activator and repressor forms of the transcription factor Cubitus interruptus (Ci). This study is based on a thermodynamic approach, which provides expression rates for these genes. These expression rates are controlled by transcription factors which are competing and cooperating for common binding sites. We have made mathematical representations of the different expression rates which depend on multiple factors and variables. The expressions obtained with the model have been refined to produce simpler equivalent formulae which allow for their mathematical analysis. Thanks to this, we can evaluate the correlation between the different interactions involved in transcription and the biological features observed at tissular level. These mathematical models can be applied to other morphogenes to help understand the complex transcriptional logic of opposing activator and repressor gradients.

PMID:
30615641
PMCID:
PMC6322776
DOI:
10.1371/journal.pone.0209349
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Public Library of Science Icon for PubMed Central
Loading ...
Support Center