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Viral proteins as a potential driver of histone depletion in dinoflagellates.

Nat Commun. 2018; 
IrwinNicholas A T,MartinBenjamin J E,YoungBarry P,BrowneMartin J G,FlausAndrew,LoewenChristopher J R,KeelingPatrick J,HoweLeA
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Codon Optimization DVNP.5 from the dinoflagellate Hematodinium sp. (accession number: AFY23231.1) was codon optimized for expression in S. cerevisiae and synthesized by GenScript into a pUC57 vector8. Membranes were incubated with the following primary antibodies: HA (Roche, High affinity 3F10 clone, 1:2500, 16h, 4°C), Pgk1 (Novex, 459250, 1:10,000, 1h, 20°C), H3 (Genscript, rabbit polyclonal raised to antigen CKDIKLARRLRGERS, 1:5000, 16h, 4°C), H4 (Abcam, ab31830, 1:2000, 16h, 4° C), or H2B (Active Motif, 39237, 1:2000, 16h, 4°C). Get A Quote

摘要

Within canonical eukaryotic nuclei, DNA is packaged with highly conserved histone proteins into nucleosomes, which facilitate DNA condensation and contribute to genomic regulation. Yet the dinoflagellates, a group of unicellular algae, are a striking exception to this otherwise universal feature as they have largely abandoned histones and acquired apparently viral-derived substitutes termed DVNPs (dinoflagellate-viral-nucleoproteins). Despite the magnitude of this transition, its evolutionary drivers remain unknown. Here, using Saccharomyces cerevisiae as a model, we show that DVNP impairs growth and antagonizes chromatin by localizing to histone binding sites, displacing nucleosomes, and impa... More

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