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The Tet family of dioxygenase enzymes convert 5-methylcytosine to 5-hydroxymethylcytosine, 5-formylcytosine and 5-carboxylcytosine, which has an effect on gene expression; here the structure of NgTet1, a Tet-like protein with the same activity as mammalian Tet1, is determined, showing that NgTet1 uses a base-flipping mechanism to access 5-methylcytosine.
Intermolecular Coulombic decay transfers excess energy to neighbouring molecules, which then lose a low-energy (and, hence, genotoxic) electron; here the process is experimentally confirmed to be site-selective and highly efficient, possibly enabling more targeted radiation therapy.
A highly specific chemical crosslinking method is used to trap a complex between an acyl carrier protein and a fatty acid dehydratase during fatty acid biosynthesis; subsequent X-ray crystallography, NMR spectroscopy and molecular dynamics simulations techniques enable the detailed study of this complex.
RecA bundles are shown to be important for the pairing of homologous loci that have segregated to opposite ends of the cell during DNA double-strand break repair in vivo in Escherichia coli.
This large comparative phylogenetic study across angiosperms shows that species that are herbaceous or have small conduits evolved these traits before colonizing environments with freezing conditions, whereas deciduous species changed their climate niche before becoming deciduous.
Applying a very large magnetic field to charge-neutral monolayer graphene produces a symmetry-protected quantum spin Hall state with helical edge states whose properties can be modulated by balancing the applied field against an intrinsic antiferromagnetic instability.
Cryo-electron microscopy combined with chemical crosslinking and mass spectrometry is used to determine the structure of the large subunit of the mammalian mitoribosome; this structure provides detailed structural insight, particularly of the molecular architecture of the polypeptide exit site, which has been structurally remodelled during evolution, presumably to help facilitate the membrane insertion of the highly hydrophobic proteins encoded by the mitochondrial genome.
This study shows that aprataxin, encoded by a gene mutated in the neurodegenerative disorder AOA1, can remove the 5′ AMP from RNA–DNA junctions; this RNA–DNA damage response promotes cell survival.
Intermolecular Coulombic decay driven by resonant Auger decay can be used to produce low-energy electrons selectively from chosen molecular or atomic sites and with tunable energies, with possible applications in radiation therapy.