Evidence map›Paper›PMID 31530634›Full record

ArticleG3 (Bethesda, Md.)2019

Transgenic Analyses in Drosophila Reveal That mCORL1 Is Functionally Distinct from mCORL2 and dCORL.

Michael J Stinchfield, Keiji Miyazawa, Stuart J Newfeld

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. 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

3 authors.

Michael J StinchfieldSchool of Life Sciences, Arizona State University, Tempe, AZ 85287-4501 and.
Keiji MiyazawaDepartment of Biochemistry, University of Yamanashi, Chuo, Yamanashi, 409-3898 Japan.
Stuart J NewfeldSchool of Life Sciences, Arizona State University, Tempe, AZ 85287-4501 and newfeld@asu.edu.ORCID 0000-0003-1400-7978

Funding

Resource for marking clones on the fly 4th chromosomeR21OD024794 · OD · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI NEWFELD, STUART J · 2017 to 2018
$488k
Automated Confocal Instrument for Core Imaging FacilityS10RR023691 · NCRR · UNIVERSITY OF UTAH · PI KAPLAN, JERRY · 2007 to 2007
$424k
NCRR NIH HHS S10 RR023691NIH HHS R21 OD024794
6 · The paper itself

Abstract

Uncovering how new members of multigene families acquire new functions is an important topic in evolutionary and developmental genetics. CORL proteins (SKOR in mice, Fussel in humans and fussel in Flybase) are a family of CNS specific proteins related to mammalian Sno/Ski oncogenes. Drosophila CORL (dCORL) participates in TGF-β and insulin signaling during development and in adult homeostasis but roles for the two mouse CORL proteins (mCORL) are essentially unknown. A series of studies were conducted to test the hypothesis based on previous results that mCORL1 is more similar to dCORL than mCORL2. Neither an updated alignment nor ectopic expression in adult wings were able to distinguish mCORL1 or mCORL2 from dCORL. Transgene experiments employing a dCORL endogenous function in mushroom body neurons showed that mCORL1 is distinct from mCORL2 and dCORL. mCORL1 and mCORL2 are also distinct in biochemical assays of Smad-binding and BMP signaling. Taken together, the data suggests testable new hypotheses for mCORL2 function in mammalian TGF-β and insulin signaling based on known roles for dCORL. Overall, the study reiterates the value of transgenic methods in Drosophila to provide new information on multigene family evolution and the function of family members in other species.

Indexed as

AnimalsDrosophilaDrosophila ProteinsInsulinMiceNerve Tissue ProteinsNeuronsProto-Oncogene ProteinsRepressor ProteinsTransforming Growth Factor betaTransgenesWings, AnimalCorl1 protein, mouseCorl2 protein, mouseDrosophila Proteinsfuss protein, DrosophilaInsulinNerve Tissue ProteinsProto-Oncogene ProteinsRepressor ProteinsTransforming Growth Factor betaFussel/SKOR/CORLgene duplicationmushroom body neuronsneofunctionalizationSno homology domain

Identifiers

PMID31530634
PMCPMC6829133

What OpenQuestion holds

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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.