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Multifactorial profiling of epigenetic landscapes at single-cell resolution using MulTI-Tag
被引:33
|作者:
Meers, Michael P.
[1
,3
]
Llagas, Geneva
[1
]
Janssens, Derek H.
[1
]
Codomo, Christine A.
[1
,2
]
Henikoff, Steven
[1
,2
]
机构:
[1] Fred Hutchinson Canc Res Ctr, Basic Sci Div, Seattle, WA 98109 USA
[2] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
[3] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
基金:
美国国家卫生研究院;
关键词:
CHROMATIN ACCESSIBILITY;
HISTONE METHYLATION;
MASS CYTOMETRY;
PRC2;
DYNAMICS;
REGULATORS;
H3K36ME3;
BINDING;
STATES;
GENES;
D O I:
10.1038/s41587-022-01522-9
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
A scalable barcoding method measures multiple chromatin-associated proteins in single cells. Chromatin profiling at locus resolution uncovers gene regulatory features that define cell types and developmental trajectories, but it remains challenging to map and compare different chromatin-associated proteins in the same sample. Here we describe Multiple Target Identification by Tagmentation (MulTI-Tag), an antibody barcoding approach for profiling multiple chromatin features simultaneously in single cells. We optimized MulTI-Tag to retain high sensitivity and specificity, and we demonstrate detection of up to three histone modifications in the same cell: H3K27me3, H3K4me1/2 and H3K36me3. We apply MulTI-Tag to resolve distinct cell types and developmental trajectories; to distinguish unique, coordinated patterns of active and repressive element regulatory usage associated with differentiation outcomes; and to uncover associations between histone marks. Multifactorial epigenetic profiling holds promise for comprehensively characterizing cell-specific gene regulatory landscapes in development and disease.
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页码:708 / +
页数:33
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