Genetics, epigenetics and disease

View Genetics, epigenetics and disease

Presenter: Adrian Bird

Published: February 2013

Age: 18-22 and upwards

Views: 1273 views

Tags: genetics epigenetics disease

Type: Lectures

Source/institution: Royal Society

Watch now

The human genome sequence has been available for more than a decade, but its significance is still not fully understood. While most human genes have been identified, there is much to learn about the DNA signals that control them. This lecture described an unusually short DNA sequence, just two base pairs long, CG, which occurs in several chemically different forms. Defects in signalling by CG are implicated in disease. For example, the autism spectrum disorder Rett syndrome is caused by loss of a protein that reads methylated CG and affects the activity of genes.Adrian Bird CBE FMedSci FRS is the Buchanan Chair of Genetics at the University of Edinburgh.The Royal Society GlaxoSmithKline Prize Lecture is awarded for original contributions to medical and veterinary sciences published within ten years from the date of the award.

You may also like

Helix – Episode 5 – Down Syndrome
Undergraduate presentations

Helix – Episode 8 – Wilson Disease
Undergraduate presentations

Mitochondrial DNA Testing

View more