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Temporal recording of mammalian development and precancer


AUTHORS

Islam MMirazul , Yang YYilin , Simmons AJAlan J , Shah VMVishal M , Musale KPKrushna Pavan , Xu YYanwen , Tasneem NNaila , Chen ZZhengyi , Trinh LTLinh T , Molina PPaola , Ramirez-Solano MAMarisol A , Sadien IDIannish D , Dou JJinzhuang , Rolong AAndrea , Chen KKen , Magnuson MAMark A , Rathmell JCJeffrey C , Macara IGIan G , Winton DJDouglas J , Liu QQi , Zafar HHamim , Kalhor RReza , Church GMGeorge M , Shrubsole MJMartha J , Coffey RJRobert J , Lau KSKen S . Nature. 2024 10 30; 634(8036). 1187-1195

ABSTRACT

Temporal ordering of cellular events offers fundamental insights into biological phenomena. Although this is traditionally achieved through continuous direct observations, an alternative solution leverages irreversible genetic changes, such as naturally occurring mutations, to create indelible marks that enables retrospective temporal ordering. Using a multipurpose, single-cell CRISPR platform, we developed a molecular clock approach to record the timing of cellular events and clonality in vivo, with incorporation of cell state and lineage information. Using this approach, we uncovered precise timing of tissue-specific cell expansion during mouse embryonic development, unconventional developmental relationships between cell types and new epithelial progenitor states by their unique genetic histories. Analysis of mouse adenomas, coupled to multiomic and single-cell profiling of human precancers, with clonal analysis of 418 human polyps, demonstrated the occurrence of polyclonal initiation in 15-30% of colonic precancers, showing their origins from multiple normal founders. Our study presents a multimodal framework that lays the foundation for in vivo recording, integrating synthetic or natural indelible genetic changes with single-cell analyses, to explore the origins and timing of development and tumorigenesis in mammalian systems.