Enhancer architecture sensitizes cell specific responses to Notch gene dose via a bind and discard mechanism

Author:

Kuang Yi1ORCID,Golan Ohad2,Preusse Kristina3,Cain Brittany4,Christensen Collin J5ORCID,Salomone Joseph16,Campbell Ian4,Okwubido-Williams FearGod V4,Hass Matthew R3,Yuan Zhenyu5,Eafergan Nathanel2,Moberg Kenneth H7,Kovall Rhett A5ORCID,Kopan Raphael38,Sprinzak David2ORCID,Gebelein Brian38ORCID

Affiliation:

1. Graduate Program in Molecular and Developmental Biology, Cincinnati Children's Hospital Research Foundation, Cincinnati, United States

2. School of Neurobiology, Biochemistry and Biophysics, George S. Wise Faculty of Life Science, Tel Aviv University, Tel Aviv, Israel

3. Division of Developmental Biology, Cincinnati Children’s Hospital, Cincinnati, United States

4. Department of Biomedical Engineering, University of Cincinnati, Cincinnati, United States

5. Department of Molecular Genetics, Biochemistry and Microbiology, University of Cincinnati College of Medicine, Cincinnati, United States

6. Medical-Scientist Training Program, University of Cincinnati College of Medicine, Cincinnati, United States

7. Department of Cell Biology, Emory University and Emory University School of Medicine, Atlanta, United States

8. Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, United States

Abstract

Notch pathway haploinsufficiency can cause severe developmental syndromes with highly variable penetrance. Currently, we have a limited mechanistic understanding of phenotype variability due to gene dosage. Here, we unexpectedly found that inserting an enhancer containing pioneer transcription factor sites coupled to Notch dimer sites can induce a subset of Notch haploinsufficiency phenotypes in Drosophila with wild type Notch gene dose. Using Drosophila genetics, we show that this enhancer induces Notch phenotypes in a Cdk8-dependent, transcription-independent manner. We further combined mathematical modeling with quantitative trait and expression analysis to build a model that describes how changes in Notch signal production versus degradation differentially impact cellular outcomes that require long versus short signal duration. Altogether, these findings support a ‘bind and discard’ mechanism in which enhancers with specific binding sites promote rapid Cdk8-dependent Notch turnover, and thereby reduce Notch-dependent transcription at other loci and sensitize tissues to gene dose based upon signal duration.

Funder

National Science Foundation

National Institutes of Health

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference80 articles.

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