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      High-Throughput In Vivo Analysis of Gene Expression in Caenorhabditis elegans

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          Abstract

          Using DNA sequences 5′ to open reading frames, we have constructed green fluorescent protein (GFP) fusions and generated spatial and temporal tissue expression profiles for 1,886 specific genes in the nematode Caenorhabditis elegans. This effort encompasses about 10% of all genes identified in this organism. GFP-expressing wild-type animals were analyzed at each stage of development from embryo to adult. We have identified 5′ DNA regions regulating expression at all developmental stages and in 38 different cell and tissue types in this organism. Among the regulatory regions identified are sequences that regulate expression in all cells, in specific tissues, in combinations of tissues, and in single cells. Most of the genes we have examined in C. elegans have human orthologs. All the images and expression pattern data generated by this project are available at WormAtlas ( http://gfpweb.aecom.yu.edu/index) and through WormBase ( http://www.wormbase.org).

          Author Summary

          Knowing where a protein is expressed provides an important clue about its potential function. As critical as this information is, we have complete developmental expression profiles for only a small fraction of all genes expressed in any metazoan. Here, we have generated spatial and temporal tissue expression profiles for 10% of all genes in the nematode Caenorhabditis elegans. Worms expressing putative gene regulatory elements fused with green fluorescent protein were analyzed at each stage of development from embryo to adult. Among the regulatory regions identified are sequences that regulate expression in all cells, in specific tissues, in combinations of tissues, and in single cells. Most of the genes we have examined in C. elegans have human orthologs. Our analysis of complex expression patterns for so many genes may not only facilitate functional analysis in C. elegans, but also create a foundation for decoding the informational hierarchies governing gene expression in all organisms.

          Abstract

          Using DNA sequences 5' to open reading frames, the authors construct green fluorescent protein fusions and generate spatial and temporal tissue expression profiles for 10% of all genes in the nematode Caenorhabditis elegans.

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          Most cited references43

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          Genome sequence of the nematode C. elegans: a platform for investigating biology.

          (1999)
          The 97-megabase genomic sequence of the nematode Caenorhabditis elegans reveals over 19,000 genes. More than 40 percent of the predicted protein products find significant matches in other organisms. There is a variety of repeated sequences, both local and dispersed. The distinctive distribution of some repeats and highly conserved genes provides evidence for a regional organization of the chromosomes.
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            A gene expression atlas of the central nervous system based on bacterial artificial chromosomes.

            The mammalian central nervous system (CNS) contains a remarkable array of neural cells, each with a complex pattern of connections that together generate perceptions and higher brain functions. Here we describe a large-scale screen to create an atlas of CNS gene expression at the cellular level, and to provide a library of verified bacterial artificial chromosome (BAC) vectors and transgenic mouse lines that offer experimental access to CNS regions, cell classes and pathways. We illustrate the use of this atlas to derive novel insights into gene function in neural cells, and into principal steps of CNS development. The atlas, library of BAC vectors and BAC transgenic mice generated in this screen provide a rich resource that allows a broad array of investigations not previously available to the neuroscience community.
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              Efficient gene transfer in C.elegans: extrachromosomal maintenance and integration of transforming sequences.

              We describe a dominant behavioral marker, rol-6(su-1006), and an efficient microinjection procedure which facilitate the recovery of Caenorhabditis elegans transformants. We use these tools to study the mechanism of C.elegans DNA transformation. By injecting mixtures of genetically marked DNA molecules, we show that large extrachromosomal arrays assemble directly from the injected molecules and that homologous recombination drives array assembly. Appropriately placed double-strand breaks stimulated homologous recombination during array formation. Our data indicate that the size of the assembled transgenic structures determines whether or not they will be maintained extrachromosomally or lost. We show that low copy number extrachromosomal transformation can be achieved by adjusting the relative concentration of DNA molecules in the injection mixture. Integration of the injected DNA, though relatively rare, was reproducibly achieved when single-stranded oligonucleotide was co-injected with the double-stranded DNA.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                PLoS Biol
                PLoS Biology
                Public Library of Science (San Francisco, USA )
                1544-9173
                1545-7885
                September 2007
                11 September 2007
                : 5
                : 9
                : e237
                Affiliations
                [1 ] Department of Zoology, University of British Columbia, Vancouver, British Columbia, Canada
                [2 ] Michael Smith Laboratories, University of British Columbia, Vancouver, British Columbia, Canada
                [3 ] Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, British Columbia, Canada
                [4 ] Genome Sciences Centre, British Columbia Cancer Agency, Vancouver, British Columbia, Canada
                [5 ] Institut für Genetik, Technische Universität Braunschweig, Braunschweig, Germany
                [6 ] Center for Genomics and Bioinformatics, Karolinska Institutet, Stockholm, Sweden
                [7 ] Department of Biosciences, Karolinska Institutet, Huddinge, Sweden
                Wellcome Trust Sanger Institute, United Kingdom
                Author notes
                * To whom correspondence should be addressed. E-mail: moerman@ 123456zoology.ubc.ca
                Article
                07-PLBI-RA-0103R3 plbi-05-09-22
                10.1371/journal.pbio.0050237
                1971126
                17850180
                a49a88d4-e5b8-472b-82c7-705021eacc9a
                Copyright: © 2007 Hunt-Newbury et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 17 January 2007
                : 5 July 2007
                Page count
                Pages: 17
                Categories
                Research Article
                Biochemistry
                Cell Biology
                Cell Biology
                Cell Biology
                Computational Biology
                Computational Biology
                Developmental Biology
                Developmental Biology
                Genetics and Genomics
                Genetics and Genomics
                Genetics and Genomics
                Molecular Biology
                Caenorhabditis
                Custom metadata
                Hunt-Newbury R, Viveiros R, Johnsen R, Mah A, Anastis D, et al. (2007) High-throughput in vivo analysis of gene expression in Caenorhabditis elegans. PLoS Biol 5(9): e237. doi: 10.1371/journal.pbio.0050237

                Life sciences
                Life sciences

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