CRISPR-Cas9 is a genome editing technology that exploits a natural bacterial defense system against phages, which are constantly invading bacteria. Bacteria defend themselves against the invaders by cutting out foreign DNA through CRISPR-Cas9, often termed ‘gene scissors’. Charpentier and colleagues managed to reprogram CRISPR-Cas9, so that it can be used as a versatile tool for editing the genome of virtually any cell. Beyond accelerating basic research, CRISPR-Cas9 is now explored as a therapy for correcting a number of human genetic diseases.
In 2011, the Charpentier laboratory identified an essential component of the CRISPR-Cas9 system, the so-called tracrRNA, which helps to recognize the piece of DNA that must be cut. This system was then developed into a precise gene-editing tool by replacing the bacterial tracrRNA, with custom-made RNAs that direct the gene scissors to any chosen location in the genome such as human cells. The details of the DNA targeting mechanism and the guidelines how to use it for gene editing were published in Science in 2012 together with Jennifer Doudna’s laboratory at the University of California, Berkeley.
Key aspects of CRISPR-Cas9 were elucidated by Emmanuelle Charpentier, first at the Max Perutz Labs and later by her research group at the Laboratory for Molecular Infection Medicine Sweden at Umeå University in Sweden. Currently Prof. Charpentier is Scientific and Managing Director of the Max Planck Unit for the Science of Pathogens, and Honorary Professor at Humboldt University, Berlin.
Read more about CRISPR/Cas9
https://www.maxperutzlabs.ac.at/research/key-discoveries/crispr/cas9-how-gene-scissors-work
Read more about Emmanuelle Charpentier and her research:
Phage therapy for treating bacterial infections: a double-edged sword
Suckers and segments of the octopus arm
Using the house mouse radiation to study the rapid evolution of genes and genetic processes
CRISPR jumps ahead: mechanistic insights into CRISPR-associated transposons
SLiMs and SHelMs: Decoding how short linear and helical motifs direct PPP specificity to direct signaling
Title to be announced
Enigmatic evolutionary origin and multipotency of the neural crest cells - major drivers of vertebrate evolution
Visualising mitotic chromosomes and nuclear dynamics by correlative light and electron microscopy
Engineered nanocarriers for imaging of small proteins by CryoEM
Bacterial cell envelope homeostasis at the (post)transcriptional level
Title to be announced
Hydrologic extremes alter mechanisms and pathways of carbon export from mountainous floodplain soils
Dissecting post-transcriptional gene expression regulation in humans and viruses
Prdm9 control of meiotic synapsis of homologs in intersubspecific hybrids
Polyploidy and rediploidisation in stressful times
Title to be announced
RNA virus from museum specimens
Programmed DNA double-strand breaks during meiosis: Mechanism and evolution
Title to be announced