Purification of Proteins Associated with Specific Genomic Loci

被引:396
|
作者
Dejardin, Jerome
Kingston, Robert E. [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Mol Biol, Boston, MA 02114 USA
关键词
BINDING PROTEINS; HUMAN TELOMERES; HUMAN-CELLS; AFFINITY PURIFICATION; MAMMALIAN-CELLS; NUCLEIC-ACID; CHROMATIN; DNA; RECOMBINATION; COMPLEX;
D O I
10.1016/j.cell.2008.11.045
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Eukaryotic DNA is bound and interpreted by numerous protein complexes in the context of chromatin. A description of the full set of proteins that regulate specific loci is critical to understanding regulation. Here, we describe a protocol called proteomics of isolated chromatin segments (PICh) that addresses this issue. PICh uses a specific nucleic acid probe to isolate genomic DNA with its associated proteins in sufficient quantity and purity to allow identification of the bound proteins. Purification of human telomeric chromatin using PICh identified the majority of known telomeric factors and uncovered a large number of novel associations. We compared proteins found at telomeres maintained by the alternative lengthening of telomeres (ALT) pathway to proteins bound at telomeres maintained by telomerase. We identified and validated several proteins, including orphan nuclear receptors, that specifically bind to ALT telomeres, establishing PICh as a useful tool for characterizing chromatin composition.
引用
收藏
页码:175 / 186
页数:12
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