Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

We use cutting-edge genomics approaches to study genetic diseases of chromatin function.

Beagrie Lab: Chromatin and Disease

More than 100 chromatin proteins have been identified as causative genes in human genetic disease. Most of these genes are broadly expressed and many have fundamental roles in transcriptional regulation, yet their disruption causes tissue-specific effects. We do not understand the molecular basis of this tissue-specificity, as it has been challenging to identify the specific cell types affected and to study the consequences of these mutations in the proper tissue context.

The Beagrie lab studies genetic disorders of chromatin function, focussing on heart and brain development because these tissues are very commonly affected in chromatin disorders. We use single-cell RNA-seq and spatial transcriptomics to identify affected cell types and the genes dysregulated in those cells. We investigate the molecular mechanisms underlying the dysregulation of these genes by assessing how chromatin organisation is affected, for example by looking for differences in the distribution of histone variants, histone modifications or nucleosome-free regions. We use Genome Architecture Mapping to measure chromatin folding, and cutting-edge computational biology techniques to identify common features of genes that are particularly sensitive to chromatin disruption.

Genome Architecture Mapping

Genome Architecture Mapping (GAM) is a technology for measuring the complex folding of DNA in the 3D space of the nucleus that Rob developed during his time with Prof. Ana Pombo. GAM works by isolating hundreds of thin slices from individual nuclei and sequencing their DNA content. Genomic regions which are close in the nucleus will be found together in the same thin nuclear slice more often than regions which are distant. Importantly, this approach is readily applicable to fixed tissue, and could therefore be an important tool for studying human disease.

 Overview of Genome Architecture Mapping

Open positions

We are always open to enquiries from interested postdocs or students - please email Rob in the first instance.

Beagrie Lab Website

Twitter: @RobBeagrie

Our team