Evidence map›Paper›PMID 10373520›Full record

ArticleMolecular and cellular biology1999

Major Egr3 isoforms are generated via alternate translation start sites and differ in their abilities to activate transcription.

K J O'Donovan, J M Baraban

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 46 citations in OpenAlex.

  1. Inducible CRISPR Epigenome Systems Mimic Cocaine Induced Bidirectional Regulation of Nab2 and Egr3.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
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  4. Expression ofAsian-Australasian journal of animal sciences · 2017
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  6. Opposing role for Egr3 in nucleus accumbens cell subtypes in cocaine action.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
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  12. Upregulation of the neuron-specific K+/Cl- cotransporter expression by transcription factor early growth response 4.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2006
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  19. Blockade of NGF-induced neurite outgrowth by a dominant-negative inhibitor of the egr family of transcription regulatory factors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2001
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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

2 authors at 2 institutions in 1 country.

K J O'DonovanDepartments of Neuroscience and Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
J M Baraban
Johns Hopkins Medicine · USJohns Hopkins University · US

Funding

UNDERSTANDING NO SIGNALING RESULTING IN NEUROPROTECTION.P50DA000266 · NIDA · JOHNS HOPKINS UNIVERSITY · PI SNYDER, SOLOMON H. · 1985 to 2017
$45.2M
PSYCHOTROPIC DRUG RESPONSIVE TRANSCRIPTION FACTORSK02DA000358 · NIDA · JOHNS HOPKINS UNIVERSITY · PI BARABAN, JAY M · 1998 to 2003
$370k
ACTIVITY DEPENDENT EXPRESSION OF EGR-3 IN BRAIN NEURONSF31DA005753 · NIDA · JOHNS HOPKINS UNIVERSITY · PI O'DONOVAN, KEVIN J · 1996 to 1998
–
NIDA NIH HHS DA00266NIDA NIH HHS DA00358NIDA NIH HHS DA05753NIDA NIH HHS F31 DA005753NIDA NIH HHS P50 DA000266
6 · The paper itself

Abstract

In previous studies, we detected a major, unidentified Egr response element (ERE) binding complex in brain extracts. We now report that this complex contains a truncated isoform of Egr3 generated by use of an alternate translation start site at methionine 106. Furthermore, the ERE binding complex previously thought to contain full-length Egr3 includes several isoforms generated by initiation at other internal methionines. Full-length and truncated (missing residues 1 to 105) Egr3 isoforms differ in the ability to stimulate transcription directed by a tandem repeat of two EREs but not by a single ERE. Taken together, our results indicate that alternative translation start sites are used to generate Egr3 isoforms with distinct transcriptional properties.

Indexed as

Alternative SplicingCodon, InitiatorProtein BiosynthesisTranscriptional ActivationAnimalsBrainCell LineDNA-Binding ProteinsEarly Growth Response Protein 3Gene ExpressionHumansMaleMethionineMiceMice, KnockoutMutagenesisCodon, InitiatorDNA-Binding ProteinsEarly Growth Response Protein 3Egr3 protein, mouseEgr3 protein, ratMethionineProtein IsoformsTranscription Factors

Identifiers

PMID10373520
PMCPMC84269
OpenAlexW2147441759

What OpenQuestion holds

Textmetadata
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.