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      The Maize TFome – development of a transcription factor open reading frame collection for functional genomics

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          Abstract

          Establishing the architecture of the gene regulatory networks (GRNs) responsible for controlling the transcription of all genes in an organism is a natural development that follows elucidation of the genome sequence. Reconstruction of the GRN requires the availability of a series of molecular tools and resources that so far have been limited to a few model organisms. One such resource consists of collections of transcription factor (TF) open reading frames (ORFs) cloned into vectors that facilitate easy expression in plants or microorganisms. In this study, we describe the development of a publicly available maize TF ORF collection (TFome) of 2034 clones corresponding to 2017 unique gene models in recombination-ready vectors that make possible the facile mobilization of the TF sequences into a number of different expression vectors. The collection also includes several hundred co-regulators (CoREGs), which we classified into well-defined families, and for which we propose here a standard nomenclature, as we have previously done for TFs. We describe the strategies employed to overcome the limitations associated with cloning ORFs from a genome that remains incompletely annotated, with a partial full-length cDNA set available, and with many TF/CoREG genes lacking experimental support. In many instances this required the combination of genome-wide expression data with gene synthesis approaches. The strategies developed will be valuable for developing similar resources for other agriculturally important plants. Information on all the clones generated is available through the GRASSIUS knowledgebase ( http://grassius.org/).

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          Most cited references42

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          Genomic libraries and a host strain designed for highly efficient two-hybrid selection in yeast.

          The two-hybrid system is a powerful technique for detecting protein-protein interactions that utilizes the well-developed molecular genetics of the yeast Saccharomyces cerevisiae. However, the full potential of this technique has not been realized due to limitations imposed by the components available for use in the system. These limitations include unwieldy plasmid vectors, incomplete or poorly designed two-hybrid libraries, and host strains that result in the selection of large numbers of false positives. We have used a novel multienzyme approach to generate a set of highly representative genomic libraries from S. cerevisiae. In addition, a unique host strain was created that contains three easily assayed reporter genes, each under the control of a different inducible promoter. This host strain is extremely sensitive to weak interactions and eliminates nearly all false positives using simple plate assays. Improved vectors were also constructed that simplify the construction of the gene fusions necessary for the two-hybrid system. Our analysis indicates that the libraries and host strain provide significant improvements in both the number of interacting clones identified and the efficiency of two-hybrid selections.
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            PlnTFDB: updated content and new features of the plant transcription factor database

            The Plant Transcription Factor Database (PlnTFDB; http://plntfdb.bio.uni-potsdam.de/v3.0/) is an integrative database that provides putatively complete sets of transcription factors (TFs) and other transcriptional regulators (TRs) in plant species (sensu lato) whose genomes have been completely sequenced and annotated. The complete sets of 84 families of TFs and TRs from 19 species ranging from unicellular red and green algae to angiosperms are included in PlnTFDB, representing >1.6 billion years of evolution of gene regulatory networks. For each gene family, a basic description is provided that is complemented by literature references, and multiple sequence alignments of protein domains. TF or TR gene entries include information of expressed sequence tags, 3D protein structures of homologous proteins, domain architecture and cross-links to other computational resources online. Moreover, the different species in PlnTFDB are linked to each other by means of orthologous genes facilitating cross-species comparisons.
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              The WRKY transcription factor superfamily: its origin in eukaryotes and expansion in plants

              Background WRKY proteins are newly identified transcription factors involved in many plant processes including plant responses to biotic and abiotic stresses. To date, genes encoding WRKY proteins have been identified only from plants. Comprehensive search for WRKY genes in non-plant organisms and phylogenetic analysis would provide invaluable information about the origin and expansion of the WRKY family. Results We searched all publicly available sequence data for WRKY genes. A single copy of the WRKY gene encoding two WRKY domains was identified from Giardia lamblia, a primitive eukaryote, Dictyostelium discoideum, a slime mold closely related to the lineage of animals and fungi, and the green alga Chlamydomonas reinhardtii, an early branching of plants. This ancestral WRKY gene seems to have duplicated many times during the evolution of plants, resulting in a large family in evolutionarily advanced flowering plants. In rice, the WRKY gene family consists of over 100 members. Analyses suggest that the C-terminal domain of the two-WRKY-domain encoding gene appears to be the ancestor of the single-WRKY-domain encoding genes, and that the WRKY domains may be phylogenetically classified into five groups. We propose a model to explain the WRKY family's origin in eukaryotes and expansion in plants. Conclusions WRKY genes seem to have originated in early eukaryotes and greatly expanded in plants. The elucidation of the evolution and duplicative expansion of the WRKY genes should provide valuable information on their functions.
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                Author and article information

                Journal
                Plant J
                Plant J
                tpj
                The Plant Journal
                BlackWell Publishing Ltd (Oxford, UK )
                0960-7412
                1365-313X
                October 2014
                26 August 2014
                : 80
                : 2
                : 356-366
                Affiliations
                [1 ]Center for Applied Plant Sciences (CAPS), The Ohio State University Columbus, OH, 43210, USA
                [2 ]Department of Biology, University of Toledo Toledo, OH, 43606, USA
                [3 ]Department of Plant Biology, Institute of Biology, State University of Campinas Campinas, Sao Paulo, 13083-970, Brazil
                [4 ]Molecular, Cellular and Developmental Biology Graduate Program, The Ohio State University Columbus, OH, 43210, USA
                [5 ]Department of Internal Medicine and The Heart and Lung Research Institute, The Ohio State University Columbus, OH, 43210, USA
                [6 ]Department of Molecular Genetics, The Ohio State University Columbus, OH, 43210, USA
                Author notes
                *For correspondence (e-mail grotewold.1@ 123456osu.edu ).
                [†]

                These authors contributed equally to this work.

                Article
                10.1111/tpj.12623
                4283594
                25053252
                b77b5d7f-0ecb-4e75-b6d3-4a4177fb2be7
                © 2014 The Authors The Plant Journal published by Society for Experimental Biology and John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

                History
                : 05 April 2014
                : 09 June 2014
                : 18 July 2014
                Categories
                Resource

                Plant science & Botany
                zea mays,maize,transcription factor,recombination-ready,yeast one-hybrid,grassius,gene regulatory network,grasses,yeast two-hybrid

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