1. 2cChIP-seq and 2cMeDIP-seq: The Carrier-Assisted Methods for Epigenomic Profiling of Small Cell Numbers or Single Cells
- Author
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Congxia Hu, Jun Wu, Pengxiao Li, Yabin Zhang, Yonglin Peng, Ruiqi Liu, Wenfei Du, Yani Kang, Jielin Sun, Ji Wu, Zhifeng Shao, and Xiaodong Zhao
- Subjects
Epigenomics ,Organic Chemistry ,Cell Count ,Sequence Analysis, DNA ,DNA ,General Medicine ,DNA Methylation ,low-input ChIP-seq ,low-input MeDIP-seq ,single-cell ChIP-seq ,female germline stem cells ,Catalysis ,Computer Science Applications ,Inorganic Chemistry ,Mice ,Animals ,Physical and Theoretical Chemistry ,Molecular Biology ,Spectroscopy - Abstract
Chromatin immunoprecipitation coupled with high-throughput sequencing (ChIP-seq) can profile genome-wide epigenetic marks associated with regulatory genomic elements. However, conventional ChIP-seq is challenging when examining limited numbers of cells. Here, we developed a new technique by supplementing carrier materials of both chemically modified mimics with epigenetic marks and dUTP-containing DNA fragments during conventional ChIP procedures (hereafter referred to as 2cChIP-seq), thus dramatically improving immunoprecipitation efficiency and reducing DNA loss of low-input ChIP-seq samples. Using this strategy, we generated high-quality epigenomic profiles of histone modifications or DNA methylation in 10–1000 cells. By introducing Tn5 transposase-assisted fragmentation, 2cChIP-seq reliably captured genomic regions with histone modification at the single-cell level in about 100 cells. Moreover, we characterized the methylome of 100 differentiated female germline stem cells (FGSCs) and observed a particular DNA methylation signature potentially involved in the differentiation of mouse germline stem cells. Hence, we provided a reliable and robust epigenomic profiling approach for small cell numbers and single cells.
- Published
- 2022
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