Prof Hallet (pictured below) described the biological and chemical basis of the CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) technique and how the development of targeted genome editing systems, such as CRISPR, and their applications has moved forward enormously in the last decade. In the last five years the field has undergone a quantum leap with the introduction of CRISPR-Cas9, the bacterial immune system which can be used to edit genomes on demand.
Bernard outlined how this serendipitous discovery that bacteria contained DNA sequences which were repeated, and interspersed with unique sequences, latterly identified as viral DNA, derived from viruses that had previously infected the bacteria.
It was then found that close to the CRISPR sequences, genes were located coding for CRISPR-associated proteins (Cas), which have nuclease activity. Together with small guide RNAs (crRNAs) which have been transcribed from the CRISPR locus, one or more Cas proteins form ribonucleoprotein targeting complexes, with each contain a single guide sequence. The Cas nuclease (usually Cas9) then cleaves the target DNA, marked for degradation by base-pairing with the crRNA.
This fabulous CRISPR-Cas9 story provides the perfect example of how basic bacterial research has moved the whole scientific community towards the next biotechnological revolution and sparked an extended Q and A after the talk itself.
Charpentier at Louvain-la-Neuve
The title Doctors Honoris Causa will be awarded by the Universite Catholique de Louvain to Prof Emmanuelle Charpentier of the Max Planck Institute for Infection Biology, Berlin, Germany for her discovery of the CRISPR/Cas9 genome editing system and to Prof Malcolm Bennett University of Nottingham, United Kingdom for his work on the root system of plants at a ceremony on 18 April.
The ceremony will take place at the UCL campus of Louvain-la-Neuve (Life Sciences Institute, ISV) on Wednesday April 18. For more information on this event and to register visit the UCL-ISV website.