A timer gene network is spatially regulated by the terminal system in the Drosophila embryo
Clark, E.; Battistara, M.; Benton, M. A.
Show abstract
In insect embryos, anteroposterior patterning is coordinated by the sequential expression of the "timer" genes caudal, Dichaete and odd-paired, whose expression dynamics correlate with the mode of segmentation. In Drosophila, the timer genes are expressed broadly across much of the blastoderm, which segments simultaneously, but their expression is delayed in a small "tail" region, just anterior to the hindgut, which segments during germband extension. Specification of the tail and the hindgut depends on the terminal gap gene tailless, but beyond this the regulation of the timer genes is poorly understood. We used a combination of multiplexed imaging, mutant analysis, and gene network modelling to resolve the regulation of the timer genes, identifying 11 new regulatory interactions and clarifying the mechanism of posterior terminal patterning. We propose that a dynamic Tailless expression gradient modulates the intrinsic dynamics of a timer gene cross-regulatory module, delineating the tail region and delaying its developmental maturation.
Matching journals
The top 2 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Maternal Wnt11b regulates cortical rotation during Xenopus axis formation: analysis of maternal-effect wnt11b mutants 97%
- Coordinated assembly and release of adhesions builds apical junctional belts during de novo polarisation of an epithelial tube 97%
- A Nodal/Eph signalling relay drives the transition from apical constriction to apico-basal shortening in ascidian endoderm invagination 97%
Similar papers in this journal
- Levels of Notch-regulated transcription are modulated by tissue movements at gastrulation 98%
- Striking parallels between dorsoventral patterning in Drosophila and Gryllus reveal a complex evolutionary history behind a model gene regulatory network 97%
- Cadherin Preserves Cohesion Across Involuting Tissues During C. elegans Neurulation 97%
Similar papers in this journal
Similar papers in this journal
- Modelling the structure of Short Gastrulation and generation of a toolkit for studying its function in Drosophila 96%
- A kinase translocation reporter reveals real-time dynamics of ERK activity in Drosophila 96%
- WntA expression and wing transcriptomics illuminate the evolution of stripe patterns in skipper butterflies 96%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.