| Mapping of clonal lineages across developmental in human neural differentiation | 
                                    
                                    
                                        | Author | 
                                        You, ZW; Wang, LY; He, H; Wu, ZY; Zhang, XY; Xue, SX; Xu, PB; Hong, YH; Xiong, M; Wei, W; Chen, YJ | 
                                    
                                    
                                        | Journal | 
                                        CELL STEM CELL | 
                                    
                                    
                                        | Pub Year | 
                                        2023 | 
                                    
                                    
                                        | Type | 
                                        Article | 
                                    
                                    
                                        
                                            
                                                | Abstract | 
                                                The cell lineages across developmental stages remain to be elucidated. Here, we developed single-cell split barcoding (SISBAR) that allows clonal tracking of single-cell transcriptomes across stages in an in vitro model of human ventral midbrain-hindbrain differentiation. We developed potential-spectiveand origin-spectiveanalyses to investigate the cross-stage lineage relationships and mapped a multi-level clonal lineage landscape depicting the whole differentiation process. We uncovered many previously unchar-acterized converging and diverging trajectories. Furthermore, we demonstrate that a transcriptome-defined cell type can arise from distinct lineages that leave molecular imprints on their progenies, and the multilineage fates of a progenitor cell-type represent the collective results of distinct rather than similar clonal fates of individual progenitors, each with distinct molecular signatures. Specifically, we uncovered a ventral midbrain progenitor cluster as the common clonal origin of midbrain dopaminergic (mDA) neurons, midbrain glutama-tergic neurons, and vascular and leptomeningeal cells and identified a surface marker that can improve graft outcomes. | 
                                            
                                        
                                    
                                    
                                        
                                            
                                                | Issue | 
                                                30 | 
                                            
                                        
                                    
                                    
                                        
                                            
                                                | Volume | 
                                                30 | 
                                            
                                        
                                    
                                    
                                        
                                            
                                                | SCI | 
                                                23.9 |