CLOCK · Characterization of the circadian chromatin landscape using a novel CRISPR/Cas9-guided proximity-labelling technique
Horizon 2020 — Marie Skłodowska-Curie Actions
- Duration
- 2020-12-01 → 2022-11-30
- EU contribution
- €162,806
- Participants
- 1
- Scheme
- MSCA-IF
Lines connect the coordinator with its partners.
Results in brief
Characterization of the circadian chromatin landscape using a novel CRISPR/Cas9-guided proximity-labelling technique
Circadian clocks are molecular oscillators present in most mammalian cells that drive the circadian rhythms (~24 h) of a wide range of molecular, physiological and behavioral functions. Circadian clocks are essential for health. In humans, their disruption (e.g. caused by shift work, jet lag, etc.) has been associated with the development of multiple pathologies (e.g. cancer, metabolic diseases such as diabetes and obesity, as well as cardiovascular and neurodegenerative diseases). In the European Union (EU) where these diseases are widespread (cardiovascular disease being the leading cause of death with 35% of all deaths, and cancer the second with 26% - according to the OECD study, 2019), understanding the basic mechanisms underlying circadian rhythmicity is therefore crucial for the development of healthcare strategies. A central aspect of molecular oscillator function is the tight regulation of circadian transcription. Over the years, several cis-regulatory proteins and enhancer elements (i.e., specific sequences located around the promoter region, e.g., E-box, RRE, D-box) have been shown to be essential for circadian transcription. However, mainly due to technical limitations, these studies have focused on a few regulators and have left many gaps in the understanding of the dynamics of circadian transcription. With recent advances in quantitative genomic-local proteomics, we saw an opportunity to overcome these limitations and sought to provide the first comprehensive and unbiased characterization of circadian protein binding to key circadian regulatory regions.
Data: CORDIS, © European Union
Project objective
To stay in synchrony with environmental cycles, most living organisms possess endogenous clocks. Circadian clocks are molecular oscillators present in most mammalian cells that drive circadian (~24 h) rhythms of a wide range of molecular, physiological and behavioral functions. Circadian clocks are essential for health. In humans their dysregulation (e.g. caused by shift work, jet lag etc.) has been associated with the development of multiple pathologies (e.g. cancer, metabolic diseases like diabetes and obesity as well as cardiovascular and neurodegenerative diseases) prevalent in the European Union.One central aspect of molecular oscillator function is the tight regulation of circadian transcription. Over the years, several proteins and cis-regulatory enhancer elements (i.e. specific sequences located around the promoter region, e.g. E-box, RRE, D-box) have been shown to be essential for circadian transcription. However, mainly because of technical limitations, those studies focused on few regulators and have left many gaps in the understanding of the dynamics of the circadian transcription. Therefore, this project proposes to use state-of-the-art quantitative genomic-locus proteomics to provide the first comprehensive and unbiased characterization of the rhythmic protein binding at key circadian regulatory regions – a key regulatory node of circadian clock function Using a CRISPR/Cas9-APEX labelling method (CASPEX), we will first characterize the circadian chromatin landscape of the three main circadian regulatory regions (i.e. E-boxes, RREs, D-boxes). We expect to find new clock modifiers, whose role for circadian rhythm generation will be investigated in a subsequent part of the project, using an RNAi-based secondary screen. Overall, this project will provide novel insights in the circadian oscillator mechanism in humans, which is essential for developing better treatment strategies for circadian clock-associated disorders.
Original text from CORDIS.
Participants
- CHARITE - UNIVERSITAETSMEDIZIN BERLIN · BerlinCoordinatorGermany
Links
Data: CORDIS, © European Union