DNA microarray technologies for measuring protein-DNA interactions

被引:102
|
作者
Bulyk, Martha L. [1 ]
机构
[1] Harvard Univ, MIT, Div Genet,Brigham & Womens Hosp, Dept Med,Dept Pathol,Div Hlth Sci & Technol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.copbio.2006.06.015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
DNA-binding proteins have key roles in many cellular processes, including transcriptional regulation and replication. Microarray-based technologies permit the high-throughput identification of binding sites and enable the functional roles of these binding proteins to be elucidated. In particular, microarray readout either of chromatin immunoprecipitated DNA-bound proteins (ChIP-chip) or of DNA adenine methyltransferase fusion proteins (DamID) enables the identification of in vivo genomic target sites of proteins. A complementary approach to analyse the in vitro binding of proteins directly to double-stranded DNA microarrays (protein binding microarrays; PBMs), permits rapid characterization of their DNA binding site sequence specificities. Recent advances in DNA microarray synthesis technologies have facilitated the definition of DNA-binding sites at much higher resolution and coverage, and advances in these and emerging technologies will further increase the efficiencies of these exciting new approaches.
引用
收藏
页码:422 / 430
页数:9
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