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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

The interaction of an ATP-dependent chromatin remodeler with a DNA ligand is described using CD spectroscopy. The induced conformational changes on a gene promoter analyzed by the peaks generated can be used to understand the mechanism of transcriptional regulation.

Abstract

Circular dichroism (CD) spectroscopy is a simple and convenient method to investigate the secondary structure and interactions of biomolecules. Recent advancements in CD spectroscopy have enabled the study of DNA-protein interactions and conformational dynamics of DNA in different microenvironments in detail for a better understanding of transcriptional regulation in vivo. The area around a potential transcription zone needs to be unwound for transcription to occur. This is a complex process requiring the coordination of histone modifications, binding of the transcription factor to DNA, and other chromatin remodeling activities. Using CD spectroscopy, it is possible to study conformational changes in the promoter region caused by regulatory proteins, such as ATP-dependent chromatin remodelers, to promote transcription. The conformational changes occurring in the protein can also be monitored. In addition, queries regarding the affinity of the protein towards its target DNA and sequence specificity can be addressed by incorporating mutations in the target DNA. In short, the unique understanding of this sensitive and inexpensive method can predict changes in chromatin dynamics, thereby improving the understanding of transcriptional regulation.

Introduction

Circular dichroism (CD) is a spectroscopic technique that relies on the inherent chirality of biological macromolecules that leads to differential absorption of right-handed and left-handed circularly polarized light. This differential absorption is known as circular dichroism. The technique, therefore, can be used to delineate the conformation of biological macromolecules, such as proteins and DNA, both of which contain chiral centers1,2.

Electromagnetic waves contain both electric and magnetic components. Both the electrical and the magnetic fields oscillate perpendicular to the d....

Protocol

1. Working concentration of the reaction components

  1. Prepare the working concentrations of buffers for CD and other reaction components freshly (see Table 1) and keep them at 4 °C before setting up the reactions.
    NOTE: For the CD reactions described in this paper, the working concentrations of components are as follows: Sodium phosphate buffer (pH 7.0) 1 mM, ATP 2 mM, DNA 500 nM, Protein 1 µM, MgCl2 10 mM, EDTA 50 mM, ADAADiN 5 µM.
<.......

Representative Results

ADAAD stabilizes a stem-loop like structure on the MYC promoter
Previous experimental evidence showed that SMARCAL1 is a negative regulator of MYC29. Analysis of the 159 bp long promoter region of the MYC gene by QGRS mapper showed that the forward strand had the potential to form a G-quadruplex (Table 2). Mfold showed that both strands of the MYC DNA could form a stem-loop-like structure .......

Discussion

The purpose of this article is to introduce the CD spectroscopy technique as an approach to study the conformational changes occurring in the DNA in the presence of ATP-dependent chromatin remodeling proteins and to link these conformational changes to gene expression. CD spectroscopy provides a fast and easily accessible method to study the conformational changes in DNA.

A crucial point to be considered for this technique is the purity of the DNA and protein. It is advisable to ensure.......

Acknowledgements

The authors would like to thank Advanced Instrumentation Research Facility, JNU, for the CD spectrophotometer. V.J. and A.D. were supported by a fellowship from CSIR.

....

Materials

NameCompanyCatalog NumberComments
2-MercaptoethanolFisher scientificO3446I-100
Adenosine 5′-triphosphate disodium salt hydrateSigmaaldrichA2383
CD Quartz CuvetteSTARNA21-Q-1
Chirascan V100 CD spectrometerApplied PhotophysicsNot available
EDTA Disodium Salt DihydrateSRL43272
Glutathione Sepharose 4BGE Healthcare17-0756-01Glutathione affinity chromatography
Hellmanex III cleaning solutionHellma9-307-011-4-507
L-Lactic DehydrogenaseSigmaaldrich L2625
Magnesium Acetate TetrahydrateFisher scientificBP215-500
Magnesium Chloride HexahydrateFisher scientificM33-500
NADH disodium saltSigmaaldrich10107735001
Phosphoenolpyruvate Monocyclohexylammonium SaltSRL40083
Potassium AcetateFisher scientificP178-3
Pyruvate KinaseSigmaaldrichP1506
Sodium Phosphate Dibasic AnhydrousFisher scientificS374-500
Sodium Phosphate Monobasic MonohydrateFisher scientificS369-500
Synergy HT microplate readerBioTekNot available
Tris BaseFisher scientificBP152-500

References

  1. Woody, R. W. Circular dichroism. Methods in Enzymology. 246, 34-71 (1995).
  2. Kelly, S., Price, N. The Use of Circular Dichroism in the Investigation of Protein Structure and Function. Current Protein & Peptide Scienc....

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