| Literature DB >> 34624206 |
Pia A Johansson1, Per Ludvik Brattås1, Christopher H Douse1, PingHsun Hsieh2, Anita Adami1, Julien Pontis3, Daniela Grassi1, Raquel Garza1, Edoardo Sozzi4, Rodrigo Cataldo5, Marie E Jönsson1, Diahann A M Atacho1, Karolina Pircs1, Feride Eren1, Yogita Sharma1, Jenny Johansson1, Alessandro Fiorenzano4, Malin Parmar4, Malin Fex5, Didier Trono3, Evan E Eichler6, Johan Jakobsson7.
Abstract
The human forebrain has expanded in size and complexity compared to chimpanzees despite limited changes in protein-coding genes, suggesting that gene expression regulation is an important driver of brain evolution. Here, we identify a KRAB-ZFP transcription factor, ZNF558, that is expressed in human but not chimpanzee forebrain neural progenitor cells. ZNF558 evolved as a suppressor of LINE-1 transposons but has been co-opted to regulate a single target, the mitophagy gene SPATA18. ZNF558 plays a role in mitochondrial homeostasis, and loss-of-function experiments in cerebral organoids suggests that ZNF558 influences developmental timing during early human brain development. Expression of ZNF558 is controlled by the size of a variable number tandem repeat that is longer in chimpanzees compared to humans, and variable in the human population. Thus, this work provides mechanistic insight into how a cis-acting structural variation establishes a regulatory network that affects human brain evolution.Entities:
Keywords: CRISPRi; KRAB-ZNFs; brain development; chimpanzee; evolution; forebrain neural progenitors; human; transposable elements
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Year: 2021 PMID: 34624206 DOI: 10.1016/j.stem.2021.09.008
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633