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      LEC1 sequentially regulates the transcription of genes involved in diverse developmental processes during seed development

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          Significance

          Seed development is biphasic, consisting of the morphogenesis phase when the basic plant body plan is established and the maturation phase when the embryo accumulates storage reserves and becomes desiccation tolerant. Despite the importance of seeds as human food and animal feed, little is known about the gene-regulatory networks that operate during these phases. We identified genes that are regulated genetically and transcriptionally by a master regulator of seed development, LEAFY COTYLEDON1 (LEC1). We show that LEC1 transcriptionally regulates genes involved in photosynthesis and other developmental processes in early and maturation genes in late seed development. Our results suggest that LEC1 partners with different transcription factors to regulate distinct gene sets and that LEC1 function is conserved in Arabidopsis and soybean seed development.

          Abstract

          LEAFY COTYLEDON1 (LEC1), an atypical subunit of the nuclear transcription factor Y (NF-Y) CCAAT-binding transcription factor, is a central regulator that controls many aspects of seed development including the maturation phase during which seeds accumulate storage macromolecules and embryos acquire the ability to withstand desiccation. To define the gene networks and developmental processes controlled by LEC1, genes regulated directly by and downstream of LEC1 were identified. We compared the mRNA profiles of wild-type and lec1-null mutant seeds at several stages of development to define genes that are down-regulated or up-regulated by the lec1 mutation. We used ChIP and differential gene-expression analyses in Arabidopsis seedlings overexpressing LEC1 and in developing Arabidopsis and soybean seeds to identify globally the target genes that are transcriptionally regulated by LEC1 in planta. Collectively, our results show that LEC1 controls distinct gene sets at different developmental stages, including those that mediate the temporal transition between photosynthesis and chloroplast biogenesis early in seed development and seed maturation late in development. Analyses of enriched DNA sequence motifs that may act as cis-regulatory elements in the promoters of LEC1 target genes suggest that LEC1 may interact with other transcription factors to regulate distinct gene sets at different stages of seed development. Moreover, our results demonstrate strong conservation in the developmental processes and gene networks regulated by LEC1 in two dicotyledonous plants that diverged ∼92 Mya.

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          Design and analysis of ChIP-seq experiments for DNA-binding proteins

          Recent progress in massively parallel sequencing platforms has allowed for genome-wide measurements of DNA-associated proteins using a combination of chromatin immunoprecipitation and sequencing (ChIP-seq). While a variety of methods exist for analysis of the established microarray alternative (ChIP-chip), few approaches have been described for processing ChIP-seq data. To fill this gap, we propose an analysis pipeline specifically designed to detect protein binding positions with high accuracy. Using three separate datasets, we illustrate new methods for improving tag alignment and correcting for background signals. We also compare sensitivity and spatial precision of several novel and previously described binding detection algorithms. Finally, we analyze the relationship between the depth of sequencing and characteristics of the detected binding positions, and provide a method for estimating the sequencing depth necessary for a desired coverage of protein binding sites.
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            Analysis of transcription factor HY5 genomic binding sites revealed its hierarchical role in light regulation of development.

            The transcription factor LONG HYPOCOTYL5 (HY5) acts downstream of multiple families of the photoreceptors and promotes photomorphogenesis. Although it is well accepted that HY5 acts to regulate target gene expression, in vivo binding of HY5 to any of its target gene promoters has yet to be demonstrated. Here, we used a chromatin immunoprecipitation procedure to verify suspected in vivo HY5 binding sites. We demonstrated that in vivo association of HY5 with promoter targets is not altered under distinct light qualities or during light-to-dark transition. Coupled with DNA chip hybridization using a high-density 60-nucleotide oligomer microarray that contains one probe for every 500 nucleotides over the entire Arabidopsis thaliana genome, we mapped genome-wide in vivo HY5 binding sites. This analysis showed that HY5 binds preferentially to promoter regions in vivo and revealed >3000 chromosomal sites as putative HY5 binding targets. HY5 binding targets tend to be enriched in the early light-responsive genes and transcription factor genes. Our data thus support a model in which HY5 is a high hierarchical regulator of the transcriptional cascades for photomorphogenesis.
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              A versatile binary vector system with a T-DNA organisational structure conducive to efficient integration of cloned DNA into the plant genome.

              A. Gleave (1992)
              A versatile gene expression cartridge and binary vector system was constructed for use in Agrobacterium-mediated plant transformation. The expression cartridge of the primary cloning vector, pART7, comprises of cauliflower mosaic virus Cabb B-JI isolate 35S promoter, a multiple cloning site and the transcriptional termination region of the octopine synthase gene. The entire cartridge can be removed from pART7 as a Not I fragment and introduced directly into the binary vector, pART27, recombinants being selected by blue/white screening for beta-galactosidase. pART27 carries the RK2 minimal replicon for maintenance in Agrobacterium, the ColE1 origin of replication for high-copy maintenance in Escherichia coli and the Tn7 spectinomycin/streptomycin resistance gene as a bacterial selectable marker. The organisational structure of the T-DNA of pART27 has been constructed taking into account the right to left border, 5' to 3' model of T-DNA transfer. The T-DNA carries the chimaeric kanamycin resistance gene (nopaline synthase promoter-neomycin phosphotransferase-nopaline synthase terminator) distal to the right border relative to the lacZ' region. Utilisation of these vectors in Agrobacterium-mediated transformation of tobacco demonstrated efficient T-DNA transfer to the plant genome.
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                Author and article information

                Journal
                Proc Natl Acad Sci U S A
                Proc. Natl. Acad. Sci. U.S.A
                pnas
                pnas
                PNAS
                Proceedings of the National Academy of Sciences of the United States of America
                National Academy of Sciences
                0027-8424
                1091-6490
                8 August 2017
                24 July 2017
                : 114
                : 32
                : E6710-E6719
                Affiliations
                [1] aDepartment of Plant Biology, University of California, Davis , CA 95616;
                [2] bDepartment of Molecular, Cell, and Developmental Biology, University of California, Los Angeles , CA 90095;
                [3] cDepartment of Plant and Microbial Biology, University of California, Berkeley , CA 94720
                Author notes
                8To whom correspondence may be addressed. Email: jjharada@ 123456ucdavis.edu or bobg@ 123456ucla.edu .

                Contributed by Robert B. Goldberg, June 27, 2017 (sent for review May 13, 2017; reviewed by Seon-kap Hwang and Brian A. Larkins)

                Author contributions: J.M.P., R.W.K., S.P., B.H.L., R.B., A.C., M.H., R.L.F., R.B.G., and J.J.H. designed research; J.M.P., R.W.K., S.P., B.H.L., R.B., A.C., M.H., M.D.M., and J.J.H. performed research; J.M.P., R.W.K., S.P., B.H.L., R.B., and J.J.H. analyzed data; and J.M.P., R.B.G., and J.J.H. wrote the paper.

                Reviewers: S.-k.H., Washington State University; and B.A.L., University of Nebraska.

                1Present address: Beckman Coulter Inc., West Sacramento, CA 95691.

                2Present address: Experiment Research Institute of National Agricultural Products Quality Management Service, Ministry of Agriculture, Food and Rural Affairs, Gimcheon, Korea.

                3Present address: Department of Botany and Plant Sciences, University of California, Riverside, CA 92521.

                4Present address: California Animal Health and Food Safety Laboratory, University of California, Davis, CA 95616.

                5Present address: Universidade Estadual do Rio Grande do Sul, Santa Cruz do Sul, Rio Grande do Sul State, Brazil.

                6Present address: Seminis, Inc., Woodland, CA 95695.

                7Present address: Bionano Genomics, Inc., San Diego, CA 92121.

                Article
                PMC5559047 PMC5559047 5559047 201707957
                10.1073/pnas.1707957114
                5559047
                28739919
                51ce412f-4cb4-416f-9647-2970ad4c1a74
                History
                Page count
                Pages: 10
                Funding
                Funded by: NSF PGRP
                Award ID: 1546806
                Funded by: DOE | SC | Basic Energy Sciences (BES) 100006151
                Award ID: DE-FG02-03ER15392
                Categories
                PNAS Plus
                Biological Sciences
                Plant Biology
                PNAS Plus

                maturation,photosynthesis, Arabidopsis ,soybean
                maturation, photosynthesis, Arabidopsis , soybean

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