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      Conserved noncoding transcription and core promoter regulatory code in early Drosophila development

      research-article
      1 , 1 ,
      eLife
      eLife Sciences Publications, Ltd
      Genome, Drosophila, Melanogaster, D. melanogaster

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          Abstract

          Multicellular development is driven by regulatory programs that orchestrate the transcription of protein-coding and noncoding genes. To decipher this genomic regulatory code, and to investigate the developmental relevance of noncoding transcription, we compared genome-wide promoter activity throughout embryogenesis in 5 Drosophila species. Core promoters, generally not thought to play a significant regulatory role, in fact impart restrictions on the developmental timing of gene expression on a global scale. We propose a hierarchical regulatory model in which core promoters define broad windows of opportunity for expression, by defining a range of transcription factors from which they can receive regulatory inputs. This two-tiered mechanism globally orchestrates developmental gene expression, including extremely widespread noncoding transcription. The sequence and expression specificity of noncoding RNA promoters are evolutionarily conserved, implying biological relevance. Overall, this work introduces a hierarchical model for developmental gene regulation, and reveals a major role for noncoding transcription in animal development.

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          Most cited references47

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          RNA maps reveal new RNA classes and a possible function for pervasive transcription.

          Significant fractions of eukaryotic genomes give rise to RNA, much of which is unannotated and has reduced protein-coding potential. The genomic origins and the associations of human nuclear and cytosolic polyadenylated RNAs longer than 200 nucleotides (nt) and whole-cell RNAs less than 200 nt were investigated in this genome-wide study. Subcellular addresses for nucleotides present in detected RNAs were assigned, and their potential processing into short RNAs was investigated. Taken together, these observations suggest a novel role for some unannotated RNAs as primary transcripts for the production of short RNAs. Three potentially functional classes of RNAs have been identified, two of which are syntenically conserved and correlate with the expression state of protein-coding genes. These data support a highly interleaved organization of the human transcriptome.
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            Transcription factors: from enhancer binding to developmental control.

            Developmental progression is driven by specific spatiotemporal domains of gene expression, which give rise to stereotypically patterned embryos even in the presence of environmental and genetic variation. Views of how transcription factors regulate gene expression are changing owing to recent genome-wide studies of transcription factor binding and RNA expression. Such studies reveal patterns that, at first glance, seem to contrast with the robustness of the developmental processes they encode. Here, we review our current knowledge of transcription factor function from genomic and genetic studies and discuss how different strategies, including extensive cooperative regulation (both direct and indirect), progressive priming of regulatory elements, and the integration of activities from multiple enhancers, confer specificity and robustness to transcriptional regulation during development.
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              • Article: not found

              A gene complex controlling segmentation in Drosophila.

              E B Lewis (1978)
              The bithorax gene complex in Drosophila contains a minimum of eight genes that seem to code for substances controlling levels of thoracic and abdominal development. The state of repression of at least four of these genes is controlled by cis-regulatory elements and a separate locus (Polycomb) seems to code for a repressor of the complex. The wild-type and mutant segmentation patterns are consistent with an antero-posterior gradient in repressor concentration along the embryo and a proximo-distal gradient along the chromosome in the affinities for repressor of each gene's cis-regulatory element.
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                Author and article information

                Contributors
                Role: Reviewing Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                20 December 2017
                2017
                : 6
                : e29005
                Affiliations
                [1 ]deptWatson School of Biological Sciences Cold Spring Harbor Laboratory New YorkUnited States
                Barcelona Supercomputing Center - BSC Spain
                Barcelona Supercomputing Center - BSC Spain
                Author notes
                [†]

                Lewis-Sigler Institute, Princeton University, Princeton, United States.

                [‡]

                Functional Genomics, Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, United States.

                Author information
                http://orcid.org/0000-0003-4250-0663
                https://orcid.org/0000-0001-9106-3573
                Article
                29005
                10.7554/eLife.29005
                5754203
                29260710
                241fc1d5-5f6d-4035-bcb1-a91a7530b6dc
                © 2017, Batut 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
                : 30 May 2017
                : 19 December 2017
                Funding
                Funded by: Cold Spring Harbor Laboratory Watson School;
                Award ID: Florence Gould Fellowship
                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
                Genes and Chromosomes
                Custom metadata
                Gene expression timing during Drosophila development is specified by multiple classes of RNA polymerase II core promoters, and the embryonic transcriptome includes thousands of evolutionarily conserved long noncoding RNAs.

                Life sciences
                genome,drosophila,melanogaster,d. melanogaster
                Life sciences
                genome, drosophila, melanogaster, d. melanogaster

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