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The INTACT method for cell type-specific gene expression and chromatin profiling in Arabidopsis thaliana
被引:264
作者:
Deal, Roger B.
[1
]
Henikoff, Steven
[1
,2
]
机构:
[1] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98104 USA
[2] Howard Hughes Med Inst, Seattle, WA USA
基金:
美国国家卫生研究院;
关键词:
STEM-CELLS;
TISSUES;
PLANTS;
DIFFERENTIATION;
IDENTIFICATION;
PATTERNS;
POSITION;
ELEGANS;
ATLAS;
ROOT;
D O I:
10.1038/nprot.2010.175
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Genomic studies of cell differentiation and function within a whole organism depend on the ability to isolate specific cell types from a tissue, but this is technically difficult. We developed a method called INTACT (isolation of nuclei tagged in specific cell types) that allows affinity-based isolation of nuclei from individual cell types of a tissue, thereby circumventing the problems associated with mechanical purification techniques. In this method nuclei are affinity-labeled through transgenic expression of a biotinylated nuclear envelope protein in the cell type of interest. Total nuclei are isolated from transgenic plants and biotin-labeled nuclei are then purified using streptavidin-coated magnetic beads, without the need for specialized equipment. INTACT gives high yield and purity of nuclei from the desired cell types, which can be used for genome-wide analysis of gene expression and chromatin features. The entire procedure, from nuclei purification through cDNA preparation or chromatin immunoprecipitation (ChIP), can be completed within 2 d. The protocol we present assumes that transgenic lines are already available, and includes procedural details for amplification of cDNA or ChIP DNA prior to microarray or deep sequencing analysis.
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页码:56 / 68
页数:13
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