染色质
计算生物学
调节器
效应器
生物
细胞生物学
基因
仿形(计算机编程)
化学
嘉雅宠物
基因表达谱
细胞
计算机科学
HEK 293细胞
基因表达调控
基因表达
分子生物学
引导RNA
作者
Wenting Xu,Xusheng Deng,Lu Qiu,Junjia Liu,Hsin‐Hui Shen,Haoran Du,Weijie Li,Linxuan Song,Wenhui Deng,Xiaoning Dong,Yi Han,B. Liu,Liming Xu,Zengpeng Li,Yongyou Zhang
标识
DOI:10.1038/s41467-026-68454-9
摘要
Conventional chromatin profiling techniques are often limited by antibody availability and performance. Here, we introduce Af-CUT&Tag, a target antibody-free method that overcomes these limitations by using CRISPR-integrated peptide tags (HiBiT/ALFA-tag) recognized by engineered binders (LgBiT/NbALFA) fused to a Tn5 transposase. Af-CUT&Tag eliminates dependence on traditional target antibodies, achieving robust specificity and sensitivity with as few as 500 cells. It provides high-quality chromatin profiles, with improved signal-to-noise ratios and library quality compared with conventional antibody-based counterparts, while also enabling single-cell resolution (scAf-CUT&Tag). Applying Af-CUT&Tag to Hippo effectors (YAP1/TAZ) during liver regeneration reveals dynamic chromatin remodeling, including YAP1/TAZ-mediated control of lipid metabolism (e.g., Lpin1, Fasn) and heme clearance (Hpx, Trf). We further identify miR-122 as a critical regulator of these processes, impacting liver regeneration. The versatility of Af-CUT&Tag in cell lines, bulk tissues, and single nuclei establishes it as a powerful tool for studying gene regulation in development, disease, and regeneration.
科研通智能强力驱动
Strongly Powered by AbleSci AI