Effect of temperature on the intrinsic flexibility of DNA and its interaction with architectural proteins

Biochemistry. 2014 Oct 21;53(41):6430-8. doi: 10.1021/bi500344j. Epub 2014 Oct 7.

Abstract

The helical structure of double-stranded DNA is destabilized by increasing temperature. Above a critical temperature (the melting temperature), the two strands in duplex DNA become fully separated. Below this temperature, the structural effects are localized. Using tethered particle motion in a temperature-controlled sample chamber, we systematically investigated the effect of increasing temperature on DNA structure and the interplay between this effect and protein binding. Our measurements revealed that (1) increasing temperature enhances DNA flexibility, effectively leading to more compact folding of the double-stranded DNA chain, and (2) temperature differentially affects different types of DNA-bending chromatin proteins from mesophilic and thermophilic organisms. Thus, our findings aid in understanding genome organization in organisms thriving at moderate as well as extreme temperatures. Moreover, our results underscore the importance of carefully controlling and measuring temperature in single-molecule DNA (micromanipulation) experiments.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Archaeal Proteins / genetics
  • Archaeal Proteins / metabolism*
  • Chromatin Assembly and Disassembly*
  • Chromosomal Proteins, Non-Histone / genetics
  • Chromosomal Proteins, Non-Histone / metabolism*
  • DNA, Archaeal / chemistry*
  • DNA, Archaeal / metabolism
  • DNA, Bacterial / chemistry*
  • DNA, Bacterial / metabolism
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Elasticity
  • Escherichia coli Proteins / metabolism*
  • Hot Temperature
  • Immobilized Nucleic Acids / chemistry
  • Immobilized Nucleic Acids / metabolism
  • Models, Biological*
  • Nucleic Acid Conformation
  • Nucleic Acid Denaturation
  • Recombinant Proteins / metabolism
  • Sulfolobus solfataricus / metabolism*

Substances

  • Archaeal Proteins
  • Chromosomal Proteins, Non-Histone
  • DNA, Archaeal
  • DNA, Bacterial
  • DNA-Binding Proteins
  • Escherichia coli Proteins
  • Immobilized Nucleic Acids
  • Recombinant Proteins
  • hns protein, E coli