A Highly Sensitive and Robust Method for Genome-wide 5hmC Profiling of Rare Cell Populations

作者：Han, Dali; Lu, Xingyu; Shih, Alan H.; Nie, Ji; You, Qiancheng; Xu, Meng Michelle; Melnick, Ari M.; Levine, Ross L.^*; He, Chuan^*

来源：Molecular Cell, 2016, 63(4): 711-719.

DOI：10.1016/j.molcel.2016.06.028

• HEMATOPOIETIC STEM
• LOW-INPUT
• CHIP-SEQ
• 5-HYDROXYMETHYLCYTOSINE
• 5-FORMYLCYTOSINE
• DEMETHYLATION
• METHYLATION
• DYNAMICS
• BLOOD
• PU.1

We present a highly sensitive and selective chemical labeling and capture approach for genome-wide profiling of 5-hydroxylmethylcytosine (5hmC) using DNA isolated from similar to 1,000 cells (nano-hmC-Seal). Using this technology, we assessed 5hmC occupancy and dynamics across different stages of hematopoietic differentiation. Nano-hmC-Seal profiling of purified Tet2-mutant acute myeloid leukemia (AML) murine stem cells allowed us to identify leukemia-specific, differentially hydroxymethylated regions that harbor known and candidate disease-specific target genes with differential 5hmC peaks compared to normal stem cells. The change of 5hmC patterns in AML strongly correlates with differential gene expression, demonstrating the importance of dynamic alterations of 5hmC in regulating transcription in AML. Together, covalent 5hmC labeling offers an effective approach to study and detect DNA methylation dynamics in in vivo disease models and in limited clinical samples.

• 出版日期2016-8-18
• 单位北京大学