| Literature DB >> 34210973 |
Murat Kirtay1, Josefine Sell2, Christian Marx1, Holger Haselmann2, Mihai Ceanga2, Zhong-Wei Zhou1,3, Vahid Rahmati2, Joanna Kirkpatrick1, Katrin Buder1, Paulius Grigaravicius1, Alessandro Ori1, Christian Geis4, Zhao-Qi Wang5,6.
Abstract
Ataxia Telangiectasia and Rad3-related (ATR) protein, as a key DNA damage response (DDR) regulator, plays an essential function in response to replication stress and controls cell viability. Hypomorphic mutations of ATR cause the human ATR-Seckel syndrome, characterized by microcephaly and intellectual disability, which however suggests a yet unknown role for ATR in non-dividing cells. Here we show that ATR deletion in postmitotic neurons does not compromise brain development and formation; rather it enhances intrinsic neuronal activity resulting in aberrant firing and an increased epileptiform activity, which increases the susceptibility of ataxia and epilepsy in mice. ATR deleted neurons exhibit hyper-excitability, associated with changes in action potential conformation and presynaptic vesicle accumulation, independent of DDR signaling. Mechanistically, ATR interacts with synaptotagmin 2 (SYT2) and, without ATR, SYT2 is highly upregulated and aberrantly translocated to excitatory neurons in the hippocampus, thereby conferring a hyper-excitability. This study identifies a physiological function of ATR, beyond its DDR role, in regulating neuronal activity.Entities:
Year: 2021 PMID: 34210973 DOI: 10.1038/s41467-021-24217-2
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919