Evidence map›Paper›PMID 25887781›Full record

ArticleBMC genomics2015

Unique patterns of transcript and miRNA expression in the South American strong voltage electric eel (Electrophorus electricus).

Lindsay L Traeger, Jeremy D Volkening, Howell Moffett, Jason R Gallant, Po-Hao Chen, Carl D Novina, George N Phillips, Rene Anand, Gregg B Wells, Matthew Pinch and 6 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.2field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  8. Genomic Survey of Tyrosine Kinases Repertoire inEvolutionary bioinformatics online · 2020
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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

16 authors at 8 institutions in 1 country.

Lindsay L TraegerDepartment of Genetics, University of Wisconsin, Madison, WI, 53706, USA. lltraeger@wisc.edu.
Jeremy D VolkeningBiotechnology Center, University of Wisconsin, Madison, WI, 53706, USA. volkening@wisc.edu.
Howell MoffettDepartment of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Boston, MA, 02115, USA. hmoffett@partners.org.
Jason R GallantDepartment of Zoology, Michigan State University, East Lansing, MI, 48824, USA. jgallant@msu.edu.
Po-Hao ChenDepartment of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Boston, MA, 02115, USA. sleepy.howard@gmail.com.
Carl D NovinaDepartment of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Boston, MA, 02115, USA. carl_novina@dfci.harvard.edu.
George N PhillipsBioSciences at Rice and Department of Chemistry, Rice University, Houston, TX, 77005, USA. georgep@rice.edu.
Rene AnandDepartment of Pharmacology and Department of Neuroscience, College of Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, 43210, USA. anand.20@osu.edu.
Gregg B WellsDepartment of Molecular and Cellular Medicine, Texas A&M University, College Station, TX, 77483, USA. gbwells@tamu.edu.
Matthew PinchDepartment of Biology, New Mexico State University, Las Cruces, NM, 88003, USA. mpinch@nmsu.edu.
Robert GüthDepartment of Biology, New Mexico State University, Las Cruces, NM, 88003, USA. rgueth@nmsu.edu.
Graciela A UnguezDepartment of Biology, New Mexico State University, Las Cruces, NM, 88003, USA. gunguez@nmsu.edu.
James S AlbertDepartment of Biology, University of Louisiana, Lafayette, LA, 70503, USA. jalbert@louisiana.edu.
Harold ZakonBEACON Center for the Study of Evolution in Action, Lansing, USA. h.zakon@austin.utexas.edu.
Michael R SussmanBiotechnology Center, University of Wisconsin, Madison, WI, 53706, USA. msussman@wisc.edu.
Manoj P SamantaSystemix Institute, Redmond, WA, 98053, USA. manoj.samanta@systemix.org.
Dana-Farber Cancer Institute · USNew Mexico State University · USUniversity of Wisconsin–Madison · USMichigan State University · USRice University · USTexas A&M University · USThe Ohio State University Wexner Medical Center · USUniversity of Louisiana at Lafayette · US

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007133 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI PERNA, NICOLE T · 1985 to 2023
$16.5M
Evolution of sodium channel genesR01GM084879 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI ZAKON, HAROLD H · 2008 to 2011
$1.4M
Fish Electric Organ as a Factory for Membrane ProteinsR01GM088670 · NIGMS · OHIO STATE UNIVERSITY · PI ANAND, RENE · 2009 to 2012
$1.2M
Molecular Mechanisms of Neuronal-dependent Muscle PlasticitySC1GM092297 · NIGMS · NEW MEXICO STATE UNIVERSITY LAS CRUCES · PI UNGUEZ, GRACIELA ALEXANDRA · 2011 to 2014
$1.1M
NIGMS NIH HHS 1SC1GM092297-01A1NIGMS NIH HHS R01 GM084879NIGMS NIH HHS R01 GM088670NIGMS NIH HHS SC1 GM092297NIGMS NIH HHS T32 GM007133
6 · The paper itself

Abstract

backgroundWith its unique ability to produce high-voltage electric discharges in excess of 600 volts, the South American strong voltage electric eel (Electrophorus electricus) has played an important role in the history of science. Remarkably little is understood about the molecular nature of its electric organs.

resultsWe present an in-depth analysis of the genome of E. electricus, including the transcriptomes of eight mature tissues: brain, spinal cord, kidney, heart, skeletal muscle, Sachs' electric organ, main electric organ, and Hunter's electric organ. A gene set enrichment analysis based on gene ontology reveals enriched functions in all three electric organs related to transmembrane transport, androgen binding, and signaling. This study also represents the first analysis of miRNA in electric fish. It identified a number of miRNAs displaying electric organ-specific expression patterns, including one novel miRNA highly over-expressed in all three electric organs of E. electricus. All three electric organ tissues also express three conserved miRNAs that have been reported to inhibit muscle development in mammals, suggesting that miRNA-dependent regulation of gene expression might play an important role in specifying an electric organ identity from its muscle precursor. These miRNA data were supported using another complete miRNA profile from muscle and electric organ tissues of a second gymnotiform species.

conclusionsOur work on the E. electricus genome and eight tissue-specific gene expression profiles will greatly facilitate future research on determining the coding and regulatory sequences that specify the function, development, and evolution of electric organs. Moreover, these data and future studies will be informed by the first comprehensive analysis of miRNA expression in an electric fish presented here.

Indexed as

TranscriptomeAnimalsElectric OrganElectrophorusMicroRNAsRNA, MessengerSouth AmericaMicroRNAsRNA, Messenger

Identifiers

PMID25887781
PMCPMC4393597
OpenAlexW2016184947

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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.