Time-resolved Microscopy of Chromatin In Vitro and In Vivo


  • Posted on the website on 6 December 2004.

*To whom correspondence should be addressed: Department of Chemistry, University of california, Riverside, CA 92521, USA. Fax: 951-827-4713; e-mail; christopher.bardeen@ucr.edu


In eukaryotic cell nuclei, double-stranded DNA is found in the form of chromatin, a large fiber made up of DNA complexed to histone proteins. In this article, recent studies using fluorescence techniques to look at the dynamics of chromatin, both in vivo and in vitro, are reviewed. Two-photon counter-propagating fluorescence recovery after patterned photobleaching is used to examine chromatin fluctuations on lengthscales ranging from less than 100 nm to microns. By combining in vivo studies with data on isolated nuclei and by measuring how these fluctuations depend on variables like ionic strength and photochemical cross-linking, it is demonstrated that the relatively large-scale motions of chromatin observed in vivo are consistent with smaller scale modifications of the histone-DNA interaction. This connection may provide a means to use conformational dynamics as an in vivo probe of the biochemical events involved in gene expression.