Budding yeast chromatin is dispersed in a crowded nucleoplasm in vivo

Author:

Chen Chen1,Lim Hong Hwa23,Shi Jian1,Tamura Sachiko4,Maeshima Kazuhiro4,Surana Uttam523,Gan Lu1

Affiliation:

1. Department of Biological Sciences and Centre for BioImaging Sciences, National University of Singapore, Singapore 117543, Singapore

2. Institute of Molecular and Cell Biology, Agency for Science Technology and Research, Proteos, Singapore 138673, Singapore

3. Bioprocessing Technology Institute, Singapore 138668, Singapore

4. National Institute of Genetics and Sokendai, Graduate University for Advanced Studies, Mishima, Shizuoka 411-8540, Japan

5. Department of Pharmacology, National University of Singapore, Singapore 117543, Singapore

Abstract

Chromatin organization has an important role in the regulation of eukaryotic systems. Although recent studies have refined the three-dimensional models of chromatin organization with high resolution at the genome sequence level, little is known about how the most fundamental units of chromatin—nucleosomes—are positioned in three dimensions in vivo. Here we use electron cryotomography to study chromatin organization in the budding yeast Saccharomyces cerevisiae. Direct visualization of yeast nuclear densities shows no evidence of 30-nm fibers. Aside from preribosomes and spindle microtubules, few nuclear structures are larger than a tetranucleosome. Yeast chromatin does not form compact structures in interphase or mitosis and is consistent with being in an “open” configuration that is conducive to high levels of transcription. From our study and those of others, we propose that yeast can regulate its transcription using local nucleosome–nucleosome associations.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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