PLANT BIOLOGY Correction for “AtsPLA2-α nuclear relocalization by the Arabidopsis transcription factor AtMYB30 leads to repression of the plant defense response,” by Solène Froidure, Joanne Canonne, Xavier Daniel, Alain Jauneau, Christian Brière, Dominique Roby, and Susana Rivas, which was first published August 9, 2010; 10.1073/pnas.1009056107 (Proc Natl Acad Sci USA 107:15281–15286). The undersigned authors wish to note, “We acknowledge inappropriate reuse of two Ponceau images from Fig. 2B and Fig. S4 of the PNAS paper in later publications of our group (see doi.org/ 10.1105/tpc.17.00567 and doi.org/10.1371/journal.pone.0190773). We hereby confirm that the original images are those first published in PNAS. When preparing the figures for submission to PNAS, the raw images were cropped and/or stretched to match the other blots and saved in the format for submission. Unfortunately, we did not systematically archive an independent copy of each raw image, and only the final version of the figures was stored. Fig. 3 appears to have areas of unmarked splicing and background inconsistencies, but we are confident, however, in the scientific accuracy of the data despite being unable to provide the original images. “Further, we acknowledge that images of yeast colonies in Fig. S1B are indeed duplicated. Our intention was to represent the presence (or absence) of yeast growth observed with the different protein combinations. We recognize that this should have been clearly indicated in the figure legend and apologize for this omission. We have been able to retrieve the original results and prepared the revised figure below showing growth of yeast colonies expressing the different protein combinations. We apologize for any inconvenience the publication of these figures may have caused.” The corrected Fig. S1 and its corrected legend appear below. The SI has been corrected online.

Micropollutants found in aquatic environments have increasingly raised concerns with respect to their uncertain environmental fate and potentially adverse effects on human health and the environment. The biodegradability of two major representatives of the polycyclic musk fragrances, Galaxolide (HHCB) and Tonalide (AHTN), and the formation of biotransformation metabolites, were investigated with Myrioconium sp. strain UHH 1-13-18-4 and Clavariopsis aquatica, two mitosporic fungi derived from freshwater environments. A particular focus was to assess the effects of extracellular oxidoreductases such as laccases, which are produced by the investigated fungi under certain conditions, on HHCB and AHTN. The fungi converted HHCB and AHTN into various products via initial hydroxylation at different carbon positions. Further metabolism resulted in the subsequent formation of diketone, peroxide, and O-methylated derivatives. Isolated laccases of the investigated fungi were able to oxidize HHCB and AHTN and catalyzed the formation of the metabolite HHCB-lactone from HHCB. At particular environmental situations also specified within the present study, biotransformations catalyzed by fungi occurring in freshwater environments may be considered when addressing the fate of polycyclic musks in freshwater systems and potential biological effects of their degradation metabolites.

The circadian clock controls numerous physiological and molecular processes in organisms ranging from fungi to human. In plants, these processes include leaf movement, stomata opening, and expression of a large number of genes. At the core of the circadian clock, the central oscillator consists of a negative autoregulatory feedback loop that is coordinated with the daily environmental changes, and that generates the circadian rhythms of the overt processes. Phosphorylation of some of the central oscillator proteins is necessary for the generation of normal circadian rhythms of Drosophila, humans, and Neurospora, where CK1 and CK2 are emerging as the main protein kinases involved in the phosphorylation of PER and FRQ. We have previously shown that in Arabidopsis, the protein kinase CK2 can phosphorylate the clock-associated protein CIRCADIAN CLOCK ASSOCIATED 1 (CCA1) in vitro. The overexpression of one of its regulatory subunits, CKB3, affects the regulation of circadian rhythms. Whether the effects of CK2 on the clock were due to its phosphorylation of a clock component had yet to be proven. By examining the effects of constitutively expressing a mutant form of the Arabidopsis clock protein CCA1 that cannot be phosphorylated by CK2, we demonstrate here that CCA1 phosphorylation by CK2 is important for the normal functioning of the central oscillator.

Hypersensitive response (HR) is a programmed cell death that is commonly associated with disease resistance in plants. Among the different HR-related early induced genes, the AtMYB30 gene is specifically, rapidly, and transiently expressed during incompatible interactions between Arabidopsis and bacterial pathogens. Its expression was also shown to be deregulated in Arabidopsis mutants affected in the control of cell death initiation. Here, we demonstrate that overexpression in Arabidopsis and tobacco of AtMYB30 (i) accelerates and intensifies the appearance of the HR in response to different avirulent bacterial pathogens, (ii) causes HR-like responses to virulent strains, and (iii) increases resistance against different bacterial pathogens, and a virulent biotrophic fungal pathogen, Cercospora nicotianae. In antisense AtMYB30 Arabidopsis lines, HR cell death is strongly decreased or suppressed in response to avirulent bacterial strains, resistance against different bacterial pathogens decreased, and the expression of HR- and defense-related genes was altered. Taken together, these results strongly suggest that AtMYB30 is a positive regulator of hypersensitive cell death.

A novel myb oncogene homologue (AtMYB30) has been isolated by differential screening of a cDNA library prepared from Xanthomonas campestris pv. campestris (X. campestris)-inoculated Arabidopsis thaliana cells cultured in the presence of cycloheximide. AtMYB30 is a single-copy gene, and the encoded protein contains a MYB domain highly homologous to other plant and animal MYB proteins. Analyses of transcript levels in A. thaliana plants, or in cultured A. thaliana cells infected with either virulent or avirulent strains of the pathogens X. campestris and Pseudomonas syringae pv. tomato, showed that maximal levels of transcription of this gene occurred during the hypersensitive response. Furthermore, in A. thaliana mutants affected in the control of cell death initiation (lsd3, lsd4 and lsd5), constitutive expression or expression in lesion-positive plants was observed, while in suppressors of the mutations lsd5 and lsd4, AtMYB30 transcripts did not accumulate. However, AtMYB30 expression could not be detected in the lsd1 mutant, which was hyper-responsive to cell death initiators and unable to limit the extent of cell death, whatever the environmental conditions. The results presented here suggest a strong correlation between AtMYB30 and genetically controlled cell death, with a role in the initiation of cell death rather than in the limitation of its extent. Our results further indicate that the lsd mutants constitute an appropriate genetic model for studying the role of this gene in hypersensitive cell death, and their relation to different steps of the pathway(s) leading to cell death.