A human tissue screen identifies a regulator of ER secretion as a brain-size determinant

Author:

Esk Christopher1ORCID,Lindenhofer Dominik1ORCID,Haendeler Simon12ORCID,Wester Roelof A.1,Pflug Florian2ORCID,Schroeder Benoit2,Bagley Joshua A.1ORCID,Elling Ulrich1ORCID,Zuber Johannes34ORCID,von Haeseler Arndt25ORCID,Knoblich Jürgen A.14ORCID

Affiliation:

1. Institute of Molecular Biotechnology of the Austrian Academy of Science (IMBA), Vienna BioCenter (VBC), Vienna, Austria.

2. Center for Integrative Bioinformatics Vienna (CIBIV), Max F. Perutz Laboratories, University of Vienna and Medical University of Vienna, VBC, Vienna, Austria.

3. Research Institute of Molecular Pathology (IMP), VBC, Vienna, Austria.

4. Medical University of Vienna, VBC, Vienna, Austria.

5. Bioinformatics and Computational Biology, Faculty of Computer Science, University of Vienna, Vienna, Austria.

Abstract

Functional screen for microcephaly genes Genetic screens are widely used to identify regulators in biological processes. Human screens are currently limited to two-dimensional cell cultures, which lack the ability to score tissue-dependent gene function. Esk et al. combined CRISPR-Cas9 screening with barcoded cellular lineage tracing to enable loss-of-function screening in three-dimensional human cerebral organoid tissue. By testing microcephaly candidate genes, the endoplasmic reticulum was found to control extracellular matrix protein secretion regulating tissue integrity and brain size. This genetic screen in human brain tissue implicates multiple pathways in microcephaly and provides a tool for systematic testing of genes in organoids. Science , this issue p. 935

Funder

European Molecular Biology Organization

H2020 European Research Council

Austrian Academy of Sciences

Austrian Science Fund

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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