Evidence map›Paper›PMID 25579975›Full record

ArticleDevelopmental cell2015

Salvador-Warts-Hippo pathway in a developmental checkpoint monitoring helix-loop-helix proteins.

Lan-Hsin Wang, Nicholas E Baker

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 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
1.3field-weighted citation impact, top 22% 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, 34 citations in OpenAlex.

  1. Article
  2. Article
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  4. Extramacrochaetae regulates Notch signaling in thebioRxiv : the preprint server for biology · 2024
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  8. Article
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  10. Regulation of theeLife · 2018
    Article
  11. Article
  12. Emerging role of Hippo signalling pathway in bladder cancer.Journal of cellular and molecular medicine · 2018
    Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Lan-Hsin WangDepartment of Genetics, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.
Nicholas E BakerDepartment of Genetics, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA; Department of Developmental and Molecular Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA; Department of Ophthalmology and Visual Sciences, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA. Electronic address: nicholas.baker@einstein.yu.edu.
Albert Einstein College of Medicine · US

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI THOMAS E ROHAN · 1985 to 2026
$111.2M
Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
CELL-CELL INTERACTIONS IN DEVELOPING RETINAR01GM047892 · NIGMS · YESHIVA UNIVERSITY · PI BAKER, NICHOLAS E · 1992 to 2017
$6.9M
NCI NIH HHS P30 CA013330NCI NIH HHS P30CA013330NIGMS NIH HHS GM047892NIGMS NIH HHS R01 GM047892NIH HHS P40 OD018537NIH HHS P40OD018537
6 · The paper itself

Abstract

The E proteins and Id proteins are, respectively, the positive and negative heterodimer partners for the basic-helix-loop-helix protein family and as such contribute to a remarkably large number of cell-fate decisions. E proteins and Id proteins also function to inhibit or promote cell proliferation and cancer. Using a genetic modifier screen in Drosophila, we show that the Id protein Extramacrochaetae enables growth by suppressing activation of the Salvador-Warts-Hippo pathway of tumor suppressors, activation that requires transcriptional activation of the expanded gene by the E protein Daughterless. Daughterless protein binds to an intronic enhancer in the expanded gene, both activating the SWH pathway independently of the transmembrane protein Crumbs and bypassing the negative feedback regulation that targets the same expanded enhancer. Thus, the Salvador-Warts-Hippo pathway has a cell-autonomous function to prevent inappropriate differentiation due to transcription factor imbalance and monitors the intrinsic developmental status of progenitor cells, distinct from any responses to cell-cell interactions.

Indexed as

Signal TransductionAnimalsCell Cycle CheckpointsCell Cycle ProteinsCell ProliferationDrosophila melanogasterDrosophila ProteinsHippo KinasesIntracellular Signaling Peptides and ProteinsProtein KinasesProtein Serine-Threonine KinasesTranscription FactorsCell Cycle ProteinsDrosophila ProteinsHippo Kinaseshpo protein, DrosophilaIntracellular Signaling Peptides and ProteinsProtein KinasesProtein Serine-Threonine Kinasessav protein, DrosophilaTranscription Factorswts protein, Drosophila

Identifiers

PMID25579975
PMCPMC4308471
OpenAlexW2021014123

What OpenQuestion holds

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Registered trials

None linked

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.