Prevention of Unc13a cryptic splicing is sufficient to preserve memory
Tianyu CaoiD, Meghraj Singh BagheliD, Rashmi Thapa, Sishir Gautam, Aswathy Peethambaran MallikaiD, Yijun WeiiD, Xiaoke K. CheniD, Irika R. SinhaiD, Grace D. BurnsiD, Shruti RenganathaniD, Xinrui WeniD, Bo Pang, Jihee Choi, Jonathan P. LingiD, Da‐Ting LiniD, Rongsong LiuiD, Yun LiiD, Philip C. WongiD
Abstract
TDP-43 dysfunction is thought to underlie frontotemporal dementia and limbic-predominant age-related TDP-43 encephalopathy, neurodegenerative dementias currently without effective therapy. Therapeutic strategies are designed to correct individual cryptic targets of TDP-43, such as UNC13A, whereby its cryptic splicing compromises synaptic function, yet the sufficiency of such an approach to prevent memory deficits is unclear. Using a forebrain neuron-specific TDP-43 knockout mouse model that recapitulates TDP-43 dysfunction occurring during early stages of human disorders, we found here that prevention of cryptic splicing to include that of Unc13a attenuated memory deficits. We show that genetic ablation of Unc13a cryptic exon solely in such TDP-43 knockout mice is sufficient to preserve cognition, supporting the clinical value of targeting UNC13A to mitigate memory deficits. Prevention of cryptic splicing of multiple targets of TDP-43 additionally attenuate neuron loss. For optimal outcomes in TDP-43 related dementias, these findings thus strongly support strategies designed to repress cryptic splicing of multiple targets of TDP-43, including UNC13A.
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