Chromatin organisation and human disease

For our next talk, in the BDI/CHG (gen)omics Seminar series, we will be hearing from Dr Robert Beagrie, Group Leader, Wellcome Centre for Human Genetics. We’re delighted to host Rob in what promises to be a great talk!

Date: Tuesday 12 November
Time: 9:30 – 10:30
Location: BDI/OxPop Seminar Room 0

Title: Chromatin organisation and human disease

Abstract: Chromatin organisation in the nucleus is a key mediator of transcriptional regulation. DNA regulatory elements that control transcription rates are carefully packaged with specific histone proteins, accumulate characteristic epigenetic modifications and are folded in ways that either facilitate or repress production of mature mRNA. The pathways that establish proper chromatin organisation are frequently affected by de novo mutations in patients with neurodevelopmental disorders (NDDs) or congenital heart defects (CHDs). I will summarise the current state of our understanding on the mechanisms at play in chromatin syndromes, technologies that will further that understanding and the potential for therapeutic intervention.

Bio: Rob studied biochemistry at the University of Cambridge before moving to Imperial College to work on DNA structure. During his doctoral studies, he developed “Genome Architecture Mapping”, a technique for mapping the folding of chromatin in the nucleus which has particular advantages for disease applications. He then moved to Oxford and worked on epigenetics regulation of gene expression in red blood cell progenitors as a postdoctoral researcher at the Weatherall Institute. He then moved to the Centre for Human Genetics to start the “Chromatin and Disease” lab in 2022. His group apply a range of cutting-edge molecular biology techniques to understand the consequences of chromatin disruption in brain and heart development.
—————————————————————
All members of the University are welcome to join.

We also now have a mailing list –
To be added, ping genomics_bdi_whg-subscribe@maillist.ox.ac.uk (with any message), you should get a bounce-back with three options to confirm your subscription. Follow any of those options, and with a bit of luck you should be signed up!

As a reminder, the (gen)omics seminar series runs every other Tuesday morning and is intended to increase interaction between individuals working in genomics across Oxford. We encourage in-person attendance where possible. There is time for discussion over, tea, coffee and pastries after the talks.

Hybrid Option:
Please note that these meetings are closed meetings and only open to members of the University of Oxford to encourage sharing of new and unpublished data. Please respect our speakers and do not share the link with anyone outside of the university.

Microsoft Teams meeting –
Join the meeting now

Meeting ID: 342 458 973 000
Passcode: FWacuV
———————————————————————————————————
If you wish to know more or receive information related to trainings and events at BDI, please subscribe by emailing bdi-announce-subscribe@maillist.ox.ac.uk. You’ll then receive an email from SYMPA and once you reply you’ll be on the list!