Literature DB >> 25431149

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

Kellen K Andrilenas, Ashley Penvose, Trevor Siggers.   

Abstract

Protein-DNA binding is central to specificity in gene regulation, and methods for characterizing transcription factor (TF)-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.
© The Author 2014. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Keywords:  DNA-binding; diversity; microarray; multi-protein; protein-binding; specificity

Mesh:

Substances:

Year:  2014        PMID: 25431149      PMCID: PMC4366590          DOI: 10.1093/bfgp/elu046

Source DB:  PubMed          Journal:  Brief Funct Genomics        ISSN: 2041-2649            Impact factor:   4.241


  72 in total

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Journal:  Nature       Date:  2001-02-15       Impact factor: 49.962

Review 2.  Recognition of specific DNA sequences.

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Journal:  Mol Cell       Date:  2001-11       Impact factor: 17.970

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7.  Counter-selectable marker for bacterial-based interaction trap systems.

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2.  Inferring primase-DNA specific recognition using a data driven approach.

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5.  NextPBM: a platform to study cell-specific transcription factor binding and cooperativity.

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Review 8.  Transcriptional control of Arabidopsis seed development.

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