19. December 2024

Colored nuclei reveal cellular key genes Colored nuclei reveal cellular key genes

Bonn researchers show how disease-relevant genes can be identified more easily

The identification of genes involved in diseases is one of the major challenges of biomedical research. Researchers at the University of Bonn and the University Hospital Bonn (UKB) have developed a method that makes their identification much easier and faster: they light up genome sequences in the cell nucleus. In contrast to complex screenings using established methods, the NIS-Seq method can be used to investigate the genetic determinants of almost any biological process in human cells. The study has now been published in Nature Biotechnology.

Showing how the genes relevant to diseases can be identified more easily - (clockwise from top left):
Showing how the genes relevant to diseases can be identified more easily - (clockwise from top left): - Alexander Hoch, Katja Blumenstock, Marius Jentzsch, Caroline Fandrey und Prof. Jonathan Schmid-Burgk. © Felix Heyder, UKBonn
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Humans have around 20,000 genes. They determine how our body functions, how we develop and how cells multiply. “Certain genes are responsible for vital immune responses, for example, but are also involved in life-threatening inflammatory processes,” says Prof. Dr. Jonathan Schmid-Burgk, research group leader at the Institute of Clinical Chemistry and Clinical Pharmacology at the UKB and member of the Immunosensation2 Cluster of Excellence at the University of Bonn. “Our research interest is to identify these genes in order to better treat diseases.”

Conventional methods: high effort and limited spectrum

CRISPR screening methods can be used to systematically examine genes for their function in cells. “CRISPR is used to switch off a random gene in each cell,” explains Schmid-Burgk. “We then enrich the cells in which a specific biological process is altered, and identify the genes switched off.” This procedure is quite complex: for each process studied, a method to enrich relevant cells has to be established, e.g., using cell sorting machines. Another weak point: CRISPR screening does not work well in every cell type - human immune cells in particular often do not survive the multi-stage process.

New method: simple detection of colored cell nuclei with a microscope

The researchers from Bonn have now developed an optical CRISPR screening method that allows to identify...

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We would like to thank the Flow Cytometry Core Facility Flow Cytometry Core Facility of the Medical Faculty at the University of Bonn for providing support and instrumentation

Caroline I. Fandrey*, Marius Jentzsch*, Peter Konopka, Alexander Hoch, Katja Blumenstock, Afraa Zackria, Salie Maasewerd, Marta Lovotti, Dorothee J. Lapp, Florian N. Gohr, Piotr Suwara, Jędrzej Świeżewski, Lukas Rossnagel, Fabienne Gobs, Maia Cristodaro, Lina Muhandes, Rayk Behrendt, Martin C. Lam, Klaus J. Walgenbach, Tobias Bald, Florian I. Schmidt, Eicke Latz, Jonathan L. Schmid-Burgk. “NIS-Seq enables cell-type-agnostic optical perturbation screening”. Nature Biotechnology, 2024, https://doi.org/10.1038/s41587-024-02516-5

Prof. Dr. Jonathan Schmid-Burgk
Cluster of Excellence ImmunoSensation2 and TRA „Life & Health“, University of Bonn
Institute of Clinical Chemistry and Clinical Pharmacology, University Hospital Bonn 
Phone: +49 228 287-51650
E-Mail: jsb@uni-bonn.de

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