Evidence map›Paper›PMID 26477561›Full record

ArticleDevelopmental biology2016

Ribbon regulates morphogenesis of the Drosophila embryonic salivary gland through transcriptional activation and repression.

Rajprasad Loganathan, Joslynn S Lee, Michael B Wells, Elizabeth Grevengoed, Matthew Slattery, Deborah J Andrew

Abstract read
In one paragraph

Article in Developmental biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. TheGenes · 2026
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  5. Article
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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

6 authors.

Rajprasad LoganathanDepartment of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, United States.
Joslynn S LeeDepartment of Biomedical Sciences, University of Minnesota Medical School, Duluth, MN 55812, United States.
Michael B WellsDepartment of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, United States.
Elizabeth GrevengoedDepartment of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, United States.
Matthew SlatteryDepartment of Biomedical Sciences, University of Minnesota Medical School, Duluth, MN 55812, United States.
Deborah J AndrewDepartment of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, United States. Electronic address: dandrew@jhmi.edu.

Funding

TRACHEALESS AND EMBRYONIC TUBE FORMATIONR01DE012873 · NIDCR · JOHNS HOPKINS UNIVERSITY · PI ANDREW, DEBORAH J · 1999 to 2015
$5.2M
Role of Trachealess in embryonic tube formationR56DE012873 · NIDCR · JOHNS HOPKINS UNIVERSITY · PI ANDREW, DEBORAH J · 2016 to 2016
$468k
NIDCR NIH HHS NIHRO1DE012873NIDCR NIH HHS R01 DE012873
6 · The paper itself

Abstract

Transcription factors affect spatiotemporal patterns of gene expression often regulating multiple aspects of tissue morphogenesis, including cell-type specification, cell proliferation, cell death, cell polarity, cell shape, cell arrangement and cell migration. In this work, we describe a distinct role for Ribbon (Rib) in controlling cell shape/volume increases during elongation of the Drosophila salivary gland (SG). Notably, the morphogenetic changes in rib mutants occurred without effects on general SG cell attributes such as specification, proliferation and apoptosis. Moreover, the changes in cell shape/volume in rib mutants occurred without compromising epithelial-specific morphological attributes such as apicobasal polarity and junctional integrity. To identify the genes regulated by Rib, we performed ChIP-seq analysis in embryos driving expression of GFP-tagged Rib specifically in the SGs. To learn if the Rib binding sites identified in the ChIP-seq analysis were linked to changes in gene expression, we performed microarray analysis comparing RNA samples from age-matched wild-type and rib null embryos. From the superposed ChIP-seq and microarray gene expression data, we identified 60 genomic sites bound by Rib likely to regulate SG-specific gene expression. We confirmed several of the identified Rib targets by qRT-pCR and/or in situ hybridization. Our results indicate that Rib regulates cell growth and tissue shape in the Drosophila salivary gland via a diverse array of targets through both transcriptional activation and repression. Furthermore, our results suggest that autoregulation of rib expression may be a key component of the SG morphogenetic gene network.

Indexed as

AnimalsApoptosisBase SequenceBinding SitesCell DivisionCell PolarityChromatin ImmunoprecipitationCluster AnalysisConsensus SequenceCytoskeletal ProteinsDrosophila melanogasterDrosophila ProteinsEmbryo, NonmammalianGene Expression Regulation, DevelopmentalGene OntologyModels, BiologicalCytoskeletal ProteinsDrosophila ProteinsRepressor Proteinsrib protein, DrosophilaDrosophilaMorphogenesisRibbonSalivary glandSize control

Identifiers

PMID26477561
PMCPMC4750396

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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.