Receptor-DNA interactions: EMSA and footprinting


Autoria(s): Read, Jason T.; Cheng, Helen; Hendy, Stephen C.; Nelson, Colleen C.; Rennie, Paul S.
Data(s)

2009

Identificador

http://eprints.qut.edu.au/37405/

Publicador

Humana

Relação

DOI:10.1007/978-1-60327-575-0_6

Read, Jason T., Cheng, Helen, Hendy, Stephen C., Nelson, Colleen C., & Rennie, Paul S. (2009) Receptor-DNA interactions: EMSA and footprinting. In McEwan, Iain J. (Ed.) The Nuclear Receptor Superfamily : Methods and Protocols. Humana, New York, N.Y, pp. 97-122.

Fonte

Faculty of Health; Institute of Health and Biomedical Innovation

Palavras-Chave #060100 BIOCHEMISTRY AND CELL BIOLOGY #060407 Genome Structure and Regulation #110105 Medical Biochemistry - Nucleic Acids #111201 Cancer Cell Biology #Nuclear Extracts, Methylation Interference, Androgen Receptor, Probasin Promoter, EMSA
Tipo

Book Chapter

Contribuinte(s)

McEwan, Iain J.

Resumo

Defining the precise promoter DNA sequence motifs where nuclear receptors and other transcription factors bind is an essential prerequisite for understanding how these proteins modulate the expression of their specific target genes. The purpose of this chapter is to provide the reader with a detailed guide with respect to the materials and the key methods required to perform this type of DNA-binding analysis. Irrespective of whether starting with purified DNA-binding proteins or somewhat crude cellular extracts, the tried-and-true procedures described here will enable one to accurately access the capacity of specific proteins to bind to DNA as well as to determine the exact sequences and DNA contact nucleotides involved. For illustrative purposes, we primarily have used the interaction of the androgen receptor with the rat probasin proximal promoter as our model system.