共 14 条
DNase-chip: a high-resolution method to identify DNase I hypersensitive sites using tiled microarrays
被引:173
作者:

Crawford, Gregory E.
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h-index: 0
机构: NHGRI, NIH, Bethesda, MD 20892 USA

Davis, Sean
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h-index: 0
机构: NHGRI, NIH, Bethesda, MD 20892 USA

Scacheri, Peter C.
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h-index: 0
机构: NHGRI, NIH, Bethesda, MD 20892 USA

Renaud, Gabriel
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机构: NHGRI, NIH, Bethesda, MD 20892 USA

Halawi, Mohamad J.
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机构: NHGRI, NIH, Bethesda, MD 20892 USA

Erdos, Michael R.
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h-index: 0
机构: NHGRI, NIH, Bethesda, MD 20892 USA

Green, Roland
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h-index: 0
机构: NHGRI, NIH, Bethesda, MD 20892 USA

Meltzer, Paul S.
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机构: NHGRI, NIH, Bethesda, MD 20892 USA

Wolfsberg, Tyra G.
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机构: NHGRI, NIH, Bethesda, MD 20892 USA

Collins, Francis S.
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h-index: 0
机构: NHGRI, NIH, Bethesda, MD 20892 USA
机构:
[1] NHGRI, NIH, Bethesda, MD 20892 USA
[2] NimbleGen Syst Inc, Madison, WI 53711 USA
关键词:
D O I:
10.1038/NMETH888
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Mapping DNase I hypersensitive sites is an accurate method of identifying the location of gene regulatory elements, including promoters, enhancers, silencers and locus control regions. Although Southern blots are the traditional method of identifying DNase I hypersensitive sites, the conventional manual method is not readily scalable to studying large chromosomal regions, much less the entire genome. Here we describe DNase-chip, an approach that can rapidly identify DNase I hypersensitive sites for any region of interest, or potentially for the entire genome, by using tiled microarrays. We used DNase-chip to identify DNase I hypersensitive sites accurately from a representative 1% of the human genome in both primary and immortalized cell types. We found that although most DNase I hypersensitive sites were present in both cell types studied, some of them were cell-type specific. This method can be applied globally or in a targeted fashion to any tissue from any species with a sequenced genome.
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页码:503 / 509
页数:7
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