Abstract

Nucleosome organization plays a key role in the regulation of gene expression. However, despite the striking advances in the accuracy of nucleosome maps, there are still severe discrepancies on individual nucleosome positioning and how this influences gene regulation. The variability among nucleosome maps, which precludes the fine analysis of nucleosome positioning, might emerge from diverse sources. We have carefully inspected the extrinsic factors that may induce diversity by the comparison of microccocal nuclease (MNase)-Seq derived nucleosome maps generated under distinct conditions. Furthermore, we have also explored the variation originated from intrinsic nucleosome dynamics by generating additional maps derived from cell cycle synchronized and asynchronous yeast cultures. Taken together, our study has enabled us to measure the effect of noise in nucleosome occupancy and positioning and provides insights into the underlying determinants. Furthermore, we present a systematic approach that may guide the standardization of MNase-Seq experiments in order to generate reproducible genome-wide nucleosome patterns.

Highlights

  • Eukaryotic chromatin is organized in a compact, precisely regulated, but yet not fully understood manner

  • Many genome-wide nucleosome maps are available in the literature for model organisms, but the correlation among the aligned maps is typically poor

  • It is difficult to determine at what extent such variability is due to biological sources or related to experimental procedures

Read more

Summary

Introduction

Eukaryotic chromatin is organized in a compact, precisely regulated, but yet not fully understood manner. The most pervasive regions depleted in nucleosomes appear upstream the transcription start site (TSS), at gene promoters Such nucleosome-free regions (NFRs) are often flanked by two nucleosomes, one very strongly located downstream TSS (+1 position), and a second one more weakly located upstream (À1 position) [14,15,8,10,13]. The integrity of this organization seems to be crucial for a correct gene regulation [16,17,18], since the introduction of a high-affinity nucleosome binding sequence in a promoter region can inhibit transcription [19]

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call