Evidence map›Paper›PMID 19937380›Full record

ArticleTransgenic research2010

Widespread expression of the Supv3L1 mitochondrial RNA helicase in the mouse.

Erin Paul, Marissa Kielbasinski, John M Sedivy, Carlos Murga-Zamalloa, Hemant Khanna, Jan E Klysik

Open access · greenAbstract read
In one paragraph

Article in Transgenic research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 46% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

6 authors at 2 institutions in 1 country.

Erin PaulDepartment of Molecular Biology, Cell Biology and Biochemistry, Brown University, 70 Ship St., Providence, RI 02903, USA.
Marissa Kielbasinski
John M Sedivy
Carlos Murga-Zamalloa
Hemant Khanna
Jan E Klysik
Brown University · USUniversity of Michigan–Ann Arbor · US

Funding

WNT SIGNALING IN HEPATOCELLULAR CARCINOMAP20RR015578 · NCRR · BROWN UNIVERSITY · PI THOMPSON, WILLIAM ALBERT · 2000 to 2009
$22.8M
X-LINKED RETINITIS PIGMENTOSAR01EY007961 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KHANNA, HEMANT · 1994 to 2009
$4.3M
X-LINKED OCULAR ALBINISM &RETINITIS PIGMENTOSAR29EY007961 · NEI · YALE UNIVERSITY · PI SWAROOP, ANAND · 1989 to 1993
–
NCRR NIH HHS 5P20RR015578-07NCRR NIH HHS P20 RR015578NEI NIH HHS EY007961NEI NIH HHS R01 EY007961
6 · The paper itself

Abstract

Supv3L1 is an evolutionarily conserved helicase that plays a critical role in the mitochondrial RNA surveillance and degradation machinery. Conditional ablation of Supv3L1 in adult mice leads to premature aging phenotypes including loss of muscle mass and adipose tissue and severe skin abnormalities. To get insights into the spatial and temporal expression of Supv3L1 in the mouse, we generated knock-in and transgenic strains in which an EGFP reporter was placed under control of the Supv3L1 native promoter. During development, expression of Supv3L1 begins at the blastocyst stage, becomes widespread and strong in all fetal tissues and cell types, and continues during postnatal growth. In mature animals reporter expression is only slightly diminished in most tissues and continues to be highly expressed in the brain, peripheral sensory organs, and testis. Together, these data confirm that Supv3L1 is an important developmentally regulated gene, which continues to be expressed in all mature tissues, particularly the rapidly proliferating cells of testes, but also in the brain and sensory organs. The transgenic mice and cell lines derived from them constitute a valuable tool for the examination of the spatial and temporal aspects of Supv3L1 promoter activity, and should facilitate future screens for small molecules that regulate Supv3L1 expression.

Indexed as

AnimalsCells, CulturedDEAD-box RNA HelicasesFemaleGene ExpressionGene Expression Regulation, DevelopmentalGene Transfer TechniquesGreen Fluorescent ProteinsMaleMiceMice, TransgenicMitochondrial ProteinsModels, BiologicalPregnancyTissue DistributionDEAD-box RNA Helicasesenhanced green fluorescent proteinGreen Fluorescent ProteinsMitochondrial ProteinsSupv3L1 protein, mouse

Identifiers

PMID19937380
PMCPMC2888911
OpenAlexW2060666370

What OpenQuestion holds

Textmetadata
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Read underepoch 390

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.