Genetic Engineering of Regulatory Evolution

GenRevo aims to uncover how regulatory sequences influence gene expression and phenotypes by re-engineering bat wing genetics in mice, advancing understanding of non-coding DNA's role in evolution and disease.

Subsidie
€ 2.490.354
2022

Projectdetails

Introduction

The regulation of genes is generally accepted to play a key role in shaping phenotypes. However, how regulatory sequences encode complex morphological structures remains unsolved. This is due to our lack of understanding of how enhancers, promoters, and other regulatory components work together to control and fine-tune gene expression.

Challenges in Gene Regulation

As such, one of the major challenges of the post-genomic era is to uncover the sequence code that controls gene expression and, ultimately, the phenotype.

Project Overview

In GenRevo, I propose to study the genomics of an extreme example of evolutionary adaptation, the wings of bats, as a model system to identify and functionally dissect how sequence determines phenotype. Our approach involves the genetic re-engineering of bat regulatory sequences in mice and their functional dissection to identify the essential components that govern gene expression and phenotype.

Methodology

Based on an already generated comprehensive data set from mouse and bat limb buds, we will detect, re-engineer, and dissect intra- and interspecies differences in regulatory landscapes linked to bat wing development. In particular, we will:

  1. Determine what non-coding features are essential for maintenance and/or change in gene expression.
  2. Reconstitute bat-specific regulatory landscapes in mice by genome engineering synthetically produced large DNA sequences.
  3. Dissect how genomic changes translate into altered gene expression and phenotypes on a cellular and regulatory level.
  4. Create de novo designer regulatory landscapes that can be used as a testbed for experimental perturbations.

Expected Outcomes

Collectively, GenRevo will produce groundbreaking knowledge in our understanding of how gene regulatory units work in vivo and how variants influence phenotypes. The possibility to re-engineer sequences in another species will spark a technological revolution in the functional analysis of mammalian genomes, particularly regarding the function of non-coding DNA in human diseases, traits, and evolution.

Financiële details & Tijdlijn

Financiële details

Subsidiebedrag€ 2.490.354
Totale projectbegroting€ 2.490.354

Tijdlijn

Startdatum1-11-2022
Einddatum31-10-2027
Subsidiejaar2022

Partners & Locaties

Projectpartners

  • CHARITE - UNIVERSITAETSMEDIZIN BERLINpenvoerder
  • MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV

Land(en)

Germany

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