Small RNAs
In plants, RNA interference spreads to neighbouring cells and the vasculature through mobile RNAs, but their identity was unclear. Dunoyer et al. found that Arapidopsis with no Dicer-like 4 (DCL4), which processes 21-nucleotide RNAs, lacked 21-nucleotide RNAs and thus silencing of SULPHUR (SUL) mRNA (targeted in this system). DCL4 rescue in companion cells (in the phloem) resulted in 21-nucleotide RNA production in leaves, confirming that they are mobile. Molnar et al. showed that 24-nucleotide RNAs are also mobile silencing elements. By grafting Arapidopsis thaliana roots to shoots they found that the roots accumulated 24-nucleotide RNAs from the shoots and that these mediated epigenetic reprogramming.
Protein structure
Two studies provide insight into the structure of the GTPases dynamin and dynamin-like myxovirus resistance protein 1 (MxA). Chappie et al. show that G (GTPase) domain dimerization is important for GTPase activity. They used a dynamin GTPase effector domain–G domain fusion, which dimerized in the presence of GTP or a transition mimic; this stabilized the conformation of the flexible switch regions in the catalytic core (required for GTP hydrolysis). GTP hydrolysis disengaged one of the flexible switch regions, leading to conformational changes that break up the dimer and release GDP. Gaon et al. find that oligomerization of MxA is important for function. MxA folds into an elongated four-helix bundle, making up the protein stalk. Wild-type MxA assembled as a stable tetramer in a criss-cross pattern in which each stalk contributes three interfaces; mutations in these inhibited oligomerization and MxA function.
Gene expression
Nucleosome-depleted regions in cell-cycle-regulated promoters ensure reliable gene expression in every cell cycle Bai, L. et al. Dev. Cell 18, 544–555 (2010)
Many promoters have nucleosome-depleted regions (NDRs), but their function in gene expression was unclear. The authors examined the role of NDRs in the expression of the cell cycle gene CLN2 (activated by SCB-binding factor (SBF)) in Saccharomyces cerevisiae. Transcription was activated reliably in every cell cycle when the CLN2 promoter's SBF-binding site was in an NDR. By contrast, highly variable 'on' and 'off' transcription was seen when the SBF-binding site was in a nucleosome. The authors propose that promoters are found in NDRs when unreliable gene expression may be detrimental to the cell.
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In brief. Nat Rev Mol Cell Biol 11, 387 (2010). https://doi.org/10.1038/nrm2914
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DOI: https://doi.org/10.1038/nrm2914