20 research outputs found

    A tree-ring and C-14 chronology of the key Sayan-Altai monuments

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    We present a radiocarbon chronology of key Sayan-Altai monuments from the Scythian period, based on a statistical analysis of dates produced in the 1980s and now supplemented with new dates. These new C-14 dates were produced for samples from the Tuekta-1 barrows (burial mounds) and were measured both in St. Petersburg and Groningen. These tree-ring samples were fitted to the calibration curve. Chronologies were established for the Arzhan, Tuekta-1 and Pazyryk-5 barrows. The time of the construction of the Arzhan and Pazyryk-5 barrows is the 9th and late 5th-4th centuries BC, respectively, and agrees with archaeology. According to new data obtained, the time of the Tuekta-1 barrow construction is some years older than has been accepted thus far by archaeologists.</p

    Rad51 Polymerization Reveals a New Chromatin Remodeling Mechanism

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    Rad51 protein is a well known protagonist of homologous recombination in eukaryotic cells. Rad51 polymerization on single-stranded DNA and its role in presynaptic filament formation have been extensively documented. Rad51 polymerizes also on double-stranded DNA but the significance of this filament formation remains unclear. We explored the behavior of Saccharomyces cerevisiae Rad51 on dsDNA and the influence of nucleosomes on Rad51 polymerization mechanism to investigate its putative role in chromatin accessibility to recombination machinery. We combined biochemical approaches, transmission electron microscopy (TEM) and atomic force microscopy (AFM) for analysis of the effects of the Rad51 filament on chromatinized templates. Quantitative analyses clearly demonstrated the occurrence of chromatin remodeling during nucleoprotein filament formation. During Rad51 polymerization, recombinase proteins moved all the nucleosomal arrays in front of the progressing filament. This polymerization process had a powerful remodeling effect, as Rad51 destabilized the nucleosomes along considerable stretches of DNA. Similar behavior was observed with RecA. Thus, recombinase polymerization is a powerful mechanism of chromatin remodeling. These remarkable features open up new possibilities for understanding DNA recombination and reveal new types of ATP-dependent chromatin dynamics
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