增强子
计算生物学
组蛋白
染色质
仿形(计算机编程)
表观遗传学
表观遗传学
生物
遗传学
计算机科学
基因
DNA甲基化
基因表达
操作系统
作者
Alba Font‐Tello,Nikolas Kesten,Yingtian Xie,Len Taing,Damir Varešlija,Leonie S. Young,Anis Hamid,Eliezer M. Van Allen,Christopher J. Sweeney,Evisa Gjini,Ana Lako,F. Steven Hodi,Joaquim Bellmunt,Myles Brown,Paloma Cejas,Henry W. Long
出处
期刊:Nature Protocols
[Springer Nature]
日期:2020-06-26
卷期号:15 (8): 2503-2518
被引量:20
标识
DOI:10.1038/s41596-020-0340-6
摘要
Fixed-tissue ChIP-seq for H3K27 acetylation (H3K27ac) profiling (FiTAc-seq) is an epigenetic method for profiling active enhancers and promoters in formalin-fixed, paraffin-embedded (FFPE) tissues. We previously developed a modified ChIP-seq protocol (FiT-seq) for chromatin profiling in FFPE. FiT-seq produces high-quality chromatin profiles particularly for methylated histone marks but is not optimized for H3K27ac profiling. FiTAc-seq is a modified protocol that replaces the proteinase K digestion applied in FiT-seq with extended heating at 65 °C in a higher concentration of detergent and a minimized sonication step, to produce robust genome-wide H3K27ac maps from clinical samples. FiTAc-seq generates high-quality enhancer landscapes and super-enhancer (SE) annotation in numerous archived FFPE samples from distinct tumor types. This approach will be of great interest for both basic and clinical researchers. The entire protocol from FFPE blocks to sequence-ready library can be accomplished within 4 d. This protocol describes a ChIP-seq procedure optimized for profiling H3K27 acetylation in archived formalin-fixed, paraffin-embedded (FFPE) tissues sampled through whole or macrodissected sectioning or from punched cores.
科研通智能强力驱动
Strongly Powered by AbleSci AI