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Biology subjects

Dodonova, S.

Publications and source records attributed to Dodonova, S..

2 recordsLinked to original sources

Cryo-electron tomography reveals near-native archaeal chromatin architecture

Most archaea package their genomes using histones, the evolutionary ancestors of eukaryotic chromatin proteins. Yet how archaeal chromatin is organized in cells has remained unknown. Here we provide the first high-resolution view of archaeal chromatin in a near-native state. We combine cryo-electron tomography, subtomogram averaging and single-particle cryo-electron microscopy to study chromatin released from gently lysed cells of the model archaeon Thermococcus kodakarensis. We show that archaeal chromatin is built from closed hypernucleosomes of variable length and determine structures of multiple hypernucleosome species, revealing a variable-beads-on-a-string architecture with flexible local contact geometries. We further show that chromatin organization changes with cellular state: logarithmic-phase cells are enriched in short hypernucleosomes, whereas stationary-phase cells form longer assemblies. Histone HTkB deletion shifts chromatin towards shorter hypernucleosomes in both growth phases and reduces local contact order. These results establish archaeal chromatin as a dynamic and complex system, shaped by growth phase and histone composition.

Molecular Biology↗

The interaction landscape between transcription factors and the nucleosome

Nucleosomes cover most of the genome and are thought to be displaced by transcription factors (TFs) in regions that direct gene expression. However, the modes of interaction between TFs and nucleosomal DNA remain largely unknown. Here, we use nucleosome consecutive affinity-purification systematic evolution of ligands by exponential enrichment (NCAP-SELEX) to systematically explore interactions between the nucleosome and 220 TFs representing diverse structural families. Consistently with earlier observations, we find that the vast majority of TFs have less access to nucleosomal DNA than to free DNA. The motifs recovered from TFs bound to nucleosomal and free DNA are generally similar; however, steric hindrance and scaffolding by the nucleosome result in specific positioning and orientation of the motifs. Many TFs preferentially bind close to the end of nucleosomal DNA, or to periodic positions at its solvent-exposed side. TFs often also bind nucleosomal DNA in a particular orientation, because the nucleosome breaks the local rotational symmetry of DNA. Some TFs also specifically interact with DNA located at the dyad position where only one DNA gyre is wound, whereas other TFs prefer sites spanning two DNA gyres and bind specifically to each of them. Our work reveals striking differences in TF binding to free and nucleosomal DNA, and uncovers a rich interaction landscape between the TFs and the nucleosome.

systems biology↗