作者
Xinhe Zheng,Boli Wu,Yuejia Liu,Sean Simmons,Kwanho Kim,Grace S. Clarke,Abdullah Ashiq,Joshua Park,Jiwen Li,Zhilin Wang,Liqi Tong,Qizhao Wang,Keerthi Thirtamara Rajamani,Rodrigo Muñoz-Castañeda,Shang Mu,Tianbo Qi,Yunxiao Zhang,Zi Chao Ngiam,Naoto Ohte,Carina Hanashima,Zhuhao Wu,Xiangmin Xu,Joshua Z. Levin,Xin Jin
摘要
Leveraging AAVs' versatile tropism and labeling capacity, we expanded the scale of in vivo CRISPR screening with single-cell transcriptomic phenotyping across embryonic to adult brains and peripheral nervous systems. Through extensive tests of 86 vectors across AAV serotypes combined with a transposon system, we substantially amplified labeling efficacy and accelerated in vivo gene delivery from weeks to days. Our proof-of-principle in utero screen identified the pleiotropic effects of Foxg1, highlighting its tight regulation of distinct networks essential for cell fate specification of Layer 6 corticothalamic neurons. Notably, our platform can label >6% of cerebral cells, surpassing the current state-of-the-art efficacy at <0.1% by lentivirus, to achieve analysis of over 30,000 cells in one experiment and enable massively parallel in vivo Perturb-seq. Compatible with various phenotypic measurements (single-cell or spatial multi-omics), it presents a flexible approach to interrogate gene function across cell types in vivo, translating gene variants to their causal function.