Positioning of nucleosomes within the 30nm fiber is fundamental in understanding how
DNA compaction regulates gene expression. Numerous studies have focused on determining the
structure, however; no studies have assessed the structure genome-wide. In this study, a new in
silico methodology for genome-wide nucleosome arrangement was assessed through the use of
randomly generating in silico datasets for the solenoid, solenoid-interdigitated, cross-linker (with
odd and even n), twisted ribbon, and twisted ribbon-interdigitated. A PERL script was written to
generate six in silico datasets from the human genome based on patterns and probabilities of close
proximity nucleosomes, and align various length terminal ends of the sequences to the genome. A
graphical representation was used to assess the genome-wide pattern of paired sequence
alignments for each model. Whole genome sequence data from formaldehyde fixed HeLa cells
were filtered, aligned, and compared to the models. Lack of sufficient experimental alignments
yielded inconclusive model determination. / DNA compaction and the 30nm chromatin fiber -- Development of in silico method for analysis of the 30nm fiber on a genome-wide scale -- Experimental analysis of the 30nm chromatin fiber on a genome-wide scale -- Future directions. / Department of Biology
| Identifer | oai:union.ndltd.org:BSU/oai:cardinalscholar.bsu.edu:123456789/196136 |
| Date | 21 July 2012 |
| Creators | Fortriede, Joshua D. |
| Contributors | Litt, Michael D., Blakey, Cynthia A. |
| Source Sets | Ball State University |
| Detected Language | English |
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