(Georgia Institute of Technology, 2019-05-10)
Kim, Harold D.; Georgia Institute of Technology. Institute for Electronics and Nanotechnology; Georgia Institute of Technology. School of Physics
(Georgia Institute of Technology, 2012-03-13)
Kim, Harold D.; Georgia Institute of Technology. Institute for Bioengineering and Bioscience; Georgia Institute of Technology. School of Physics
In eukaryotes, the genomic DNA is highly packaged inside the nucleus of a cell by forming
beads-on-a string-like structure called nucleosomes. The propensity of a ~150-bp duplex
DNA to form a nucleosome, termed the "nucleosome affinity", varies over a few orders of
magnitude depending on the DNA sequence. Although nucleosome affinity is thought to be
determined by DNA bending stiffness, the exact relationship between the two is not clear.
Besides their role in DNA packaging, nucleosomes can repress gene expression by
preventing transcription factors from accessing their DNA binding sites. Some nucleosomes,
however, do not directly occlude transcription factor binding sites, and therefore their role in
gene expression remains unknown. In the first part of this talk, I will explain how we
measure looping kinetics and permanent curvature of various sequences of DNA using
single-molecule FRET (fluorescence resonance energy transfer) and gel electrophoresis. I
will then estimate nucleosome affinity of different sequences based on these measurements.
In the second part, I will explain how we quantify gene expression pattern using
fluorescence microscopy of yeast cells and demonstrate two examples where a nucleosome
exhibits opposite effects on gene expression. Based on these results, I will present a model
for nucleosome removal prior to transcription initiation.