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Takemata, N.

Publications and source records attributed to Takemata, N..

3 recordsLinked to original sources

Reverse gyrase and 3D genome architecture suppress hyperthermophile genome instability arising from horizontal gene transfer

Reverse gyrase (Rgy), a distinctive topoisomerase conserved in all hyperthermophiles, has the unique ability to introduce positive DNA supercoils. It has long been hypothesized that Rgy overwinds genomic DNA to prevent its detrimental denaturation at high temperature. However, its role in vivo has remained unresolved for more than four decades. In the course of investigating how Rgy affects genome organization in the archaeon Thermococcus kodakarensis, we find that Rgy suppresses heat-induced clustering of AT-rich genes, most of which bear signatures of horizontal gene transfer. This function depends on the topoisomerase active site of Rgy, underscoring a critical role of its action on DNA topology. The clustering of AT-rich genes is accompanied by their aberrant recruitment of the single-stranded DNA-binding protein RPA, indicative of extensive DNA melting. Genetic analysis further provides evidence that RPA sequesters denatured loci and mitigates genome instability in the absence of Rgy. We propose that DNA topology and higher-order genome organization constitute a multilayered mechanism that stabilizes horizontally acquired genes at high temperature.

molecular biology↗

Archaeal histone HTkC hypercompacts DNA

Histones are important organizers of chromatin in eukaryotes and archaea. In eukaryotes, the core histones assemble with DNA to form the octameric nucleosome. In archaea, histones form hypernucleosomes that are not restricted to an octameric histone core but can extend to variable lengths. We previously identified face-to-face (FtF) histones as a widely distributed group of archaeal histones that assemble into toroidal tetramer structures, distinct from nucleosomal histones. Here, we characterize the FtF histone HTkC from Thermococcus kodakarensis, which also encodes the canonical histones HTkA and HTkB. We show that HTkC wraps DNA around its toroidal tetramer and forms highly compact nucleoprotein complexes, achieving a level of compaction approximately twice that of hypernucleosomes. Consistent with a major chromatin-organizing role, htkC is among the most highly expressed genes in T. kodakarensis and its deletion leads to impaired growth. Together, these findings establish FtF histones as important organizers of archaeal chromatin alongside classical histones.

biochemistry↗

Chromosomal domain formation by archaeal SMC, a roadblock protein, and DNA structure

Structural maintenance of chromosomes (SMC) complexes fold genomes by extruding DNA loops. In eukaryotes, loop-extruding SMC complexes form topologically associating domains (TADs) by being stalled by roadblock proteins. It remains unclear whether a similar mechanism of domain formation exists in prokaryotes. Using high-resolution chromosome conformation capture sequencing, we show that an archaeal homolog of the bacterial Smc-ScpAB complex organizes the genome of Thermococcus kodakarensis into TAD-like domains. We also find that TrmBL2, a nucleoid- associated protein that forms a stiff nucleoprotein filament, stalls the T. kodakarensis SMC complex and establishes a boundary at the site-specific recombination site dif. TrmBL2 stalls the SMC complex at tens of additional non-boundary loci with lower efficiency. Intriguingly, the stalling efficiency is correlated with structural properties of underlying DNA sequences. Our study illuminates not only a eukaryotic-like mechanism of domain formation in archaea, but also an unforeseen role of intrinsic DNA structure in large-scale genome organization.

molecular biology↗