Analysis of sequence Specificities of DNA-binding proteins with protein binding microarrays

被引:24
作者
Bulyk, Martha L. [1 ]
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Div Genet,Dept Med,Harvard MIT Div Hlth Sci & Tec, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Pathol,Harvard MIT Div Hlth Sci & Technol, Boston, MA 02115 USA
来源
DNA MICROARRAYS PART A: ARRAY PLATFORMS AND WET-BENCH PROTOCOLS | 2006年 / 410卷
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0076-6879(06)10013-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
DNA-binding proteins are important for various cellular processes, such as transcriptional regulation, recombination, replication, repair, and DNA modification. Of particular interest are transcription factors (TFs), since through interactions with their DNA binding sites, they modulate gene expression in a manner required for normal cellular growth and differentiation, and also for response to environmental stimuli. To date, the DNA-binding specificities of most DNA-binding proteins remain unknown, as earlier technologies aimed at characterizing DNA-protein interactions have been laborious and not highly scalable. New DNA microarray-based technology, termed protein binding microarrays (PBMs), has been developed that allows rapid, high-throughput characterization of in vitro DNA binding site sequence specificities of TFs or of any DNA binding protein. DNA binding site data from PBMs can be used to predict what genes are regulated by a given TF, what the functions are of a given TF and its predicted target genes, and how that TF may fit into the transcriptional regulatory networks of the cell.
引用
收藏
页码:279 / +
页数:23
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