Evidence map›Paper›PMID 25634895›Full record

ArticleNucleic acids research2015

Genome-wide features of neuroendocrine regulation in Drosophila by the basic helix-loop-helix transcription factor DIMMED.

Tarik Hadžić, Dongkook Park, Katharine C Abruzzi, Lin Yang, Jennifer S Trigg, Remo Rohs, Michael Rosbash, Paul H Taghert

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Function of Drosophila Synaptotagmins in membrane trafficking at synapses.Cellular and molecular life sciences : CMLS · 2021
    Review
  3. A cell atlas of the adultProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  4. Article
  5. Neuropeptide Mapping of Dimmed Cells of Adult Drosophila Brain.Journal of the American Society for Mass Spectrometry · 2018
    Article
  6. Article
  7. Shep regulatesDevelopment (Cambridge, England) · 2018
    Article
  8. Article
  9. Article
  10. Article
  11. Transcriptional Reorganization ofFrontiers in molecular neuroscience · 2017
    Article
  12. Review
  13. Article
  14. TheFrontiers in molecular neuroscience · 2016
    Article
  15. Article
  16. Article
  17. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Tarik HadžićDepartment of Anatomy and Neurobiology, Washington University School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, USA.
Dongkook ParkDepartment of Anatomy and Neurobiology, Washington University School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, USA.
Katharine C AbruzziHoward Hughes Medical Institute, National Center for Behavioral Genomics, Department of Biology, Brandeis University, Waltham, MA 02454, USA.
Lin YangMolecular and Computational Biology Program, Department of Biological Sciences, University of Southern California, Los Angeles, CA 90089, USA.
Jennifer S TriggDepartment of Anatomy and Neurobiology, Washington University School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, USA.
Remo RohsMolecular and Computational Biology Program, Department of Biological Sciences, University of Southern California, Los Angeles, CA 90089, USA.
Michael RosbashHoward Hughes Medical Institute, National Center for Behavioral Genomics, Department of Biology, Brandeis University, Waltham, MA 02454, USA.
Paul H TaghertDepartment of Anatomy and Neurobiology, Washington University School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110, USA taghertp@pcg.wustl.edu.ORCID http://orcid.org/0000-0002-5399-2993
Washington University in St. Louis · USHoward Hughes Medical Institute · USUniversity of Southern California · US

Funding

THE MOLECULAR GENETIC BASIS OF SENSORY BEHAVIOR IN DROSOPHILAP01NS044232 · NINDS · BRANDEIS UNIVERSITY · PI MARDER, EVE E · 2002 to 2011
$13.2M
Washington University Center for Translational NeuroscienceP30NS057105 · NINDS · WASHINGTON UNIVERSITY · PI HOLTZMAN, DAVID M. · 2006 to 2011
$8.7M
Mouse CoreP30NS045713 · NINDS · BRANDEIS UNIVERSITY · PI ROSBASH, MICHAEL · 2003 to 2013
$7.8M
DEVELOPMENTAL REGULATION OF NEUROPEPTIDE EXPRESSIONR01NS021749 · NINDS · WASHINGTON UNIVERSITY · PI TAGHERT, PAUL H · 1985 to 2013
$4.3M
Multi-scale modeling of genetic variation in a developmental networkU01GM103804 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI DEPACE, ANGELA H, MARJORAM, PAUL · 2013 to 2016
$2.0M
Genome analysis based on the integration of DNA sequence and shapeR01GM106056 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ROHS, REMO · 2014 to 2017
$1.3M
Howard Hughes Medical InstituteNIGMS NIH HHS R01 GM106056NIGMS NIH HHS R01GM106056NIGMS NIH HHS U01 GM103804NIGMS NIH HHS U01GM103804NINDS NIH HHS P01 NS044232NINDS NIH HHS P30-NS045713NINDS NIH HHS P30 NS057105NINDS NIH HHS R01 NS021749NINDS NIH HHS R01NS21749NINDS NIH HHS R01 NS27419
6 · The paper itself

Abstract

Neuroendocrine (NE) cells use large dense core vesicles (LDCVs) to traffic, process, store and secrete neuropeptide hormones through the regulated secretory pathway. The dimmed (DIMM) basic helix-loop-helix transcription factor of Drosophila controls the level of regulated secretory activity in NE cells. To pursue its mechanisms, we have performed two independent genome-wide analyses of DIMM's activities: (i) in vivo chromatin immunoprecipitation (ChIP) to define genomic sites of DIMM occupancy and (ii) deep sequencing of purified DIMM neurons to characterize their transcriptional profile. By this combined approach, we showed that DIMM binds to conserved E-boxes in enhancers of 212 genes whose expression is enriched in DIMM-expressing NE cells. DIMM binds preferentially to certain E-boxes within first introns of specific gene isoforms. Statistical machine learning revealed that flanking regions of putative DIMM binding sites contribute to its DNA binding specificity. DIMM's transcriptional repertoire features at least 20 LDCV constituents. In addition, DIMM notably targets the pro-secretory transcription factor, creb-A, but significantly, DIMM does not target any neuropeptide genes. DIMM therefore prescribes the scale of secretory activity in NE neurons, by a systematic control of both proximal and distal points in the regulated secretory pathway.

Indexed as

AnimalsBase SequenceBasic Helix-Loop-Helix ProteinsBinding SitesChromatin ImmunoprecipitationConserved SequenceDrosophilaDrosophila ProteinsE-Box ElementsGenome, InsectHigh-Throughput Nucleotide SequencingNeuroendocrine CellsSecretory PathwaySequence Analysis, DNATrans-ActivatorsTranscriptomeBasic Helix-Loop-Helix Proteinsdimm protein, DrosophilaDrosophila ProteinsTrans-Activators

Identifiers

PMID25634895
PMCPMC4344488
OpenAlexW1966470419

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.