Evidence map›Paper›PMID 11076860›Full record

ArticleGenome research2000

Fusion of the human gene for the polyubiquitination coeffector UEV1 with Kua, a newly identified gene.

T M Thomson, J J Lozano, N Loukili, R Carrió, F Serras, B Cormand, M Valeri, V M Díaz, J Abril, M Burset and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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

48 citing papers in PubMed, 111 citations in OpenAlex.

  1. Article
  2. Review
  3. A Protocol for the Detection of Fusion Transcripts Using RNA-Sequencing Data.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  4. Article
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  7. Review
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  10. A Novel Mutation of theInternational journal of molecular sciences · 2020
    Article
  11. TheProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. Review
  13. Article
  14. Search for potential reading frameshifts in cds from Arabidopsis thaliana and other genomes.DNA research : an international journal for rapid publication of reports on genes and genomes · 2019
    Article
  15. Drosophila Argonaute2 turnover is regulated by the ubiquitin proteasome pathway.Biochemical and biophysical research communications · 2017
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 1 institution in 1 country.

T M ThomsonInstitut de Biologia Molecular, Consejo Superior de Investigaciones Cientificas, Barcelona, Spain. tthomson@hg.vhebron.es
J J Lozano
N Loukili
R Carrió
F Serras
B Cormand
M Valeri
V M Díaz
J Abril
M Burset
J Merino
A Macaya
M Corominas
R Guigó
Universidad de Cantabria · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

UEV proteins are enzymatically inactive variants of the E2 ubiquitin-conjugating enzymes that regulate noncanonical elongation of ubiquitin chains. In Saccharomyces cerevisiae, UEV is part of the RAD6-mediated error-free DNA repair pathway. In mammalian cells, UEV proteins can modulate c-FOS transcription and the G2-M transition of the cell cycle. Here we show that the UEV genes from phylogenetically distant organisms present a remarkable conservation in their exon-intron structure. We also show that the human UEV1 gene is fused with the previously unknown gene Kua. In Caenorhabditis elegans and Drosophila melanogaster, Kua and UEV are in separated loci, and are expressed as independent transcripts and proteins. In humans, Kua and UEV1 are adjacent genes, expressed either as separate transcripts encoding independent Kua and UEV1 proteins, or as a hybrid Kua-UEV transcript, encoding a two-domain protein. Kua proteins represent a novel class of conserved proteins with juxtamembrane histidine-rich motifs. Experiments with epitope-tagged proteins show that UEV1A is a nuclear protein, whereas both Kua and Kua-UEV localize to cytoplasmic structures, indicating that the Kua domain determines the cytoplasmic localization of Kua-UEV. Therefore, the addition of a Kua domain to UEV in the fused Kua-UEV protein confers new biological properties to this regulator of variant polyubiquitination.

Indexed as

Recombination, GeneticSaccharomyces cerevisiae ProteinsTranscription FactorsAmino Acid SequenceAnimalsBase SequenceBiopolymersCaenorhabditis elegansConserved SequenceGene Expression ProfilingHeLa CellsHumansIntronsJurkat CellsLigasesMiceBiopolymersLigasesPEDS1 protein, humanPolyubiquitinRAD6 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsTranscription FactorsUBE2V1 protein, humanUbiquitin-Conjugating EnzymesUbiquitins

Identifiers

PMID11076860
PMCPMC310942
OpenAlexW2151778540

What OpenQuestion holds

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Read underepoch 390

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.