Abstract
The acquisition of cellular identity during development depends on precise spatiotemporal regulation of gene expression, with combinatorial interactions between transcription factors, accessory proteins and the basal transcription machinery together translating complex signaling inputs into appropriate gene expression outputs. The opposing repressive and activating inputs of the Drosophila ETS family transcription factors Yan and Pointed orchestrate numerous cell fate transitions downstream of receptor tyrosine kinase signaling, providing one of the premier systems for studying this process. Current models describe the differentiative transition as a switch from Yan-mediated repression to Pointed-mediated activation of common target genes. We describe here a new layer of regulation whereby Yan and Pointed co-occupy regulatory elements to repress gene expression in a coordinated manner, with Pointed being unexpectedly required for the genome-wide occupancy of both Yan and the co-repressor Groucho. Using even skipped as a test-case, synergistic genetic interactions between Pointed, Groucho, Yan and components of the RNA polymerase II pausing machinery suggest that Pointed integrates multiple scales of repressive regulation to confer robustness. We speculate that this mechanism may be used broadly to fine-tune the expression of many genes crucial for development.
Original language | English (US) |
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Article number | dev165985 |
Journal | Development (Cambridge) |
Volume | 145 |
Issue number | 13 |
DOIs | |
State | Published - Jul 2018 |
Funding
This work was supported by grants from the American Heart Association (12POST12040225/Jemma Webber/2012-2014 and 15POST22660028/Jemma Webber/2015 to J.L.W.) and the National Institute of General Medical Sciences (R01 GM080372 to I.R.), and by the Genomics Core Facility through a University of Chicago Cancer Center Support Grant (P30 CA014599). N.S.-L. was supported in part by the National Institute of General Medical Sciences (T32 GM007281) and the National Eye Institute (R01 EY12549 to I.R.). Deposited in PMC for release after 12 months. We thank Pieter Faber, Mikayka Marchuk and Abhilasha Cheruku in the University of Chicago Genomics Facility for help with ChIP-seq and microarray. Jean-Francois Boisclair Lachance, Kohta Ikegami, Rebecca Spokony and Matthew Slattery provided many helpful discussions and comments on the manuscript. We acknowledge the Bloomington Drosophila Stock Center (NIHP40OD018537) and the Developmental Studies Hybridoma Bank (created by the NICHD of the NIH) for reagents. Funding This work was supported by grants from the American Heart Association (12POST12040225/Jemma Webber/2012-2014 and 15POST22660028/Jemma Webber/2015 to J.L.W.) and the National Institute of General Medical Sciences (R01 GM080372 to I.R.), and by the Genomics Core Facility through a University of Chicago Cancer Center Support Grant (P30 CA014599). N.S.-L. was supported in part by the National Institute of General Medical Sciences (T32 GM007281) and the National Eye Institute (R01 EY12549 to I.R.). Deposited in PMC for release after 12 months.
Keywords
- Cell fate specification
- Chromatin occupancy
- Gene regulatory network
- Mesoderm development
- RNA pol II pausing
ASJC Scopus subject areas
- Molecular Biology
- Developmental Biology