Visualising neuronal signalling dynamics within intact neuronal circuits: Deciphering the role of cell-specific MeCP2 dynamics in neuronal function and dysfunction

Introduction

Epigenetic signalling pathways are required to translate external sensory input to neuronal gene modulation and function. Disruption of epigenetic signals leads to devastating brain pathologies. One prominent example is Rett syndrome (RTT), a postnatal neurodevelopmental disease that results in rapid deterioration of sensory, motor, cognitive, and social functions.

Background

RTT is caused by loss of function mutations in a single gene encoding for Methyl-CpG binding protein 2 (MeCP2), an abundant and multifunctional methylation reader in the brain. While transgenic mouse models of MeCP2 loss have provided significant insights into RTT, they also revealed the vast complexity of the regulation of MeCP2 signalling and cell-specific heterogeneity.

Importantly, both a deficit and a surplus of MeCP2 give rise to pathological phenotypes.

Project Goals

Here, we will develop an imaging-based approach to monitor endogenous MeCP2 signalling and dynamics in intact neuronal circuits in awake behaving mice.

Methodology

We will combine the following techniques:

1. CRISPR/Cas9 genome editing to fluorescently label endogenous MeCP2.
2. FRET-based biosensors to detect dynamic MeCP2 signalling without perturbing its innate regulation.
3. In vivo two-photon fluorescence lifetime imaging to enable dual imaging of MeCP2 signalling and concurrent neuronal activity.

Expected Outcomes

Using this approach, we will:

• Map the functional landscape of MeCP2 activity in the intact mouse brain across cell-type, circuit, and sensory experience.
• Image in vivo MeCP2 signalling in transgenic mice with common RTT mutations.

This will allow us to detect early cell-type specific MeCP2 dysfunction and avoid broad late-stage RTT symptoms.

Significance

The direct visualisation of the intricate interplay between MeCP2 signalling and neuronal function within intact neuronal circuits will be transformative. It will shed light on the physiological role of epigenetic signalling in the brain and provide vital insights for future therapeutic interventions.