Using protein-binding microarrays to study transcription factor specificity: homologs, isoforms and complexes

被引:17
作者
Andrilenas, Kellen K. [1 ]
Penvose, Ashley [1 ]
Siggers, Trevor [1 ]
机构
[1] Boston Univ, Dept Biol, Boston, MA 02115 USA
关键词
protein-binding; microarray; specificity; multi-protein; DNA-binding; diversity; DNA-BINDING; IN-VITRO; DATA REVEALS; SIMPLE CODE; SEQUENCE; RECOGNITION; INSIGHTS; IDENTIFICATION; MECHANISMS; LANDSCAPES;
D O I
10.1093/bfgp/elu046
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Protein DNA binding is central to specificity in gene regulation, and methods for characterizing transcription factor (IF) DNA binding remain crucial to studies of regulatory specificity. High-throughput (HT) technologies have revolutionized our ability to characterize protein DNA binding by significantly increasing the number of binding measurements that can be performed. Protein-binding microarrays (PBMs) are a robust and powerful HT platform for studying DNA-binding specificity of TFs. Analysis of PBM-determined DNA-binding profiles has provided new insight into the scope and mechanisms of TF binding diversity. In this review, we focus specifically on the PBM technique and discuss its application to the study of TF specificity, in particular, the binding diversity of TF homologs and multi-protein complexes.
引用
收藏
页码:17 / 29
页数:13
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