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      Arabidopsis RNA processing factor SERRATE regulates the transcription of intronless genes

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          Abstract

          Intron splicing increases proteome complexity, promotes RNA stability, and enhances transcription. However, introns and the concomitant need for splicing extend the time required for gene expression and can cause an undesirable delay in the activation of genes. Here, we show that the plant microRNA processing factor SERRATE (SE) plays an unexpected and pivotal role in the regulation of intronless genes. Arabidopsis SE associated with more than 1000, mainly intronless, genes in a transcription-dependent manner. Chromatin-bound SE liaised with paused and elongating polymerase II complexes and promoted their association with intronless target genes. Our results indicate that stress-responsive genes contain no or few introns, which negatively affects their expression strength, but that some genes circumvent this limitation via a novel SE-dependent transcriptional activation mechanism. Transcriptome analysis of a Drosophila mutant defective in ARS2, the metazoan homologue of SE, suggests that SE/ARS2 function in regulating intronless genes might be conserved across kingdoms.

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          Fast, background-free, 3D super-resolution optical fluctuation imaging (SOFI).

          Super-resolution optical microscopy is a rapidly evolving area of fluorescence microscopy with a tremendous potential for impacting many fields of science. Several super-resolution methods have been developed over the last decade, all capable of overcoming the fundamental diffraction limit of light. We present here an approach for obtaining subdiffraction limit optical resolution in all three dimensions. This method relies on higher-order statistical analysis of temporal fluctuations (caused by fluorescence blinking/intermittency) recorded in a sequence of images (movie). We demonstrate a 5-fold improvement in spatial resolution by using a conventional wide-field microscope. This resolution enhancement is achieved in iterative discrete steps, which in turn allows the evaluation of images at different resolution levels. Even at the lowest level of resolution enhancement, our method features significant background reduction and thus contrast enhancement and is demonstrated on quantum dot-labeled microtubules of fibroblast cells.
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            Ensembl Genomes 2016: more genomes, more complexity

            Ensembl Genomes (http://www.ensemblgenomes.org) is an integrating resource for genome-scale data from non-vertebrate species, complementing the resources for vertebrate genomics developed in the context of the Ensembl project (http://www.ensembl.org). Together, the two resources provide a consistent set of programmatic and interactive interfaces to a rich range of data including reference sequence, gene models, transcriptional data, genetic variation and comparative analysis. This paper provides an update to the previous publications about the resource, with a focus on recent developments. These include the development of new analyses and views to represent polyploid genomes (of which bread wheat is the primary exemplar); and the continued up-scaling of the resource, which now includes over 23 000 bacterial genomes, 400 fungal genomes and 100 protist genomes, in addition to 55 genomes from invertebrate metazoa and 39 genomes from plants. This dramatic increase in the number of included genomes is one part of a broader effort to automate the integration of archival data (genome sequence, but also associated RNA sequence data and variant calls) within the context of reference genomes and make it available through the Ensembl user interfaces.
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              Rapidly regulated genes are intron poor.

              We show that genes with rapidly changing expression levels in response to stress contain significantly lower intron densities in yeasts, thale cress and mice. Therefore, we propose that introns can delay regulatory responses and are selected against in genes whose transcripts require rapid adjustment for survival of environmental challenges. These findings could provide an explanation for the apparent extensive intron loss during the evolution of some eukaryotic lineages.
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                Author and article information

                Contributors
                Role: Reviewing Editor
                Role: Senior Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                28 August 2018
                2018
                : 7
                : e37078
                Affiliations
                [1 ]deptCentre for Plant Molecular Biology (ZMBP) University of Tuebingen TuebingenGermany
                [2 ]Chemical Genomics Centre (CGC) of the Max Planck Society DortmundGermany
                [3 ]Max Planck Institute for Developmental Biology TuebingenGermany
                [4 ]deptInstitute for Biology and Environmental Science University of Oldenburg OldenburgGermany
                [5 ]deptDepartment of Plant Physiology, Umea Plant Science Centre Umeå University UmeaSweden
                [6 ]deptProteome Centre University of Tuebingen TuebingenGermany
                School of Life Sciences, Tsinghua University China
                Harvard Medical School United States
                School of Life Sciences, Tsinghua University China
                Author information
                http://orcid.org/0000-0002-9603-0882
                http://orcid.org/0000-0003-2859-4288
                http://orcid.org/0000-0002-6682-0728
                Article
                37078
                10.7554/eLife.37078
                6135607
                30152752
                111a4bda-6f6d-49ea-b38b-59bcb9cec9dc
                © 2018, Speth et al

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

                History
                : 28 March 2018
                : 22 August 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001659, Deutsche Forschungsgemeinschaft;
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100004189, Max-Planck-Gesellschaft;
                Award Recipient :
                The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
                Categories
                Research Article
                Chromosomes and Gene Expression
                Plant Biology
                Custom metadata
                Arabidopsis RNA processing factor SERRATE associates with the chromatin of intronless genes, which are usually expressed at low levels, to enhance polymerase II association.

                Life sciences
                serrate,splicing,intron,intronless genes,transcription,a. thaliana,d. melanogaster,other
                Life sciences
                serrate, splicing, intron, intronless genes, transcription, a. thaliana, d. melanogaster, other

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