Evidence map›Paper›PMID 9405623›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1997

Inhibition of mRNA export in vertebrate cells by nuclear export signal conjugates.

A E Pasquinelli, M A Powers, E Lund, D Forbes, J E Dahlberg

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 55 citations in OpenAlex.

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  11. Splicing is required for rapid and efficient mRNA export in metazoans.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  12. Article
  13. Article
  14. A Crm1p-independent nuclear export path for the mRNA-associated protein, Npl3p/Mtr13p.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  15. Article
  16. An exon that prevents transport of a mature mRNA.Proceedings of the National Academy of Sciences of the United States of America · 1999
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  17. 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

5 authors at 2 institutions in 1 country.

A E PasquinelliDepartment of Biomolecular Chemistry, 1300 University Avenue, University of Wisconsin, Madison, WI 53706, USA.
M A Powers
E Lund
D Forbes
J E Dahlberg
University of Wisconsin–Madison · USUniversity of California, San Diego · US

Funding

FUNCTIONAL STUDY OF NATIVE AND SYNTHETIC NUCLEIR01GM033279 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FORBES, DOUGLASS JANE · 1985 to 2015
$7.0M
RNAS AND PROTEINS BETWEEN THE NUCLEUS AND CYTOPLASMR37GM030220 · NIGMS · UNIVERSITY OF WISCONSIN MADISON · PI DAHLBERG, JAMES E · 1998 to 2005
$3.1M
STRUCTURE, ORGANIZATION, AND EXPRESSION OF SNRNA GENESR01GM030220 · NIGMS · UNIVERSITY OF WISCONSIN MADISON · PI DAHLBERG, JAMES E · 1985 to 1997
–
NIGMS NIH HHS GM30220NIGMS NIH HHS GM33279NIGMS NIH HHS R01 GM033279NIGMS NIH HHS R37 GM030220
6 · The paper itself

Abstract

Leucine-rich nuclear export signals (NESs) are recognized by the NES receptor exportin 1 and are central to the export of multiple shuttling proteins and RNAs. The export of messenger RNA in vertebrates was, however, thought to occur by a different pathway, because inhibition by injection of a synthetic Rev NES conjugate could not be demonstrated. Here we find that peptide conjugates composed of the NES of either protein kinase A inhibitor protein (PKI) or the HIV-1 Rev protein, when coupled to human serum albumin, are potent inhibitors of mRNA and small nuclear RNA export. These results provide direct evidence that mRNA export in vertebrates depends on interactions between an NES and its cognate NES receptors. PKI NES conjugates are significantly more efficient at inhibiting RNA export than are REV NES conjugates, indicating that different NESs may have different abilities to promote protein and RNA export. Surprisingly, an expected control conjugate containing the mutant Rev NES sequence M10 strongly inhibited the export of intronless dihydrofolate reductase mRNA. Nuclear injection of NES peptide conjugates led to mislocalization to the nucleus of 10-20% of the cytoplasmic Ran GTPase-binding protein (RanBP1) indicating that RanBP1 shuttles between the nucleus and the cytoplasm via an NES pathway. These results demonstrate that in vertebrates the export of mRNA, like that of small nuclear RNA, 5S rRNA, and transport factors such as RanBP1, employs NES-mediated molecular machinery.

Indexed as

KaryopherinsReceptors, Cytoplasmic and NuclearAmino Acid SequenceAnimalsBiological TransportCarrier ProteinsExportin 1 ProteinFemaleGene Products, revHumansMolecular Sequence DataNuclear ProteinsRNA, MessengerTransfectionXenopus laevisCarrier ProteinsExportin 1 ProteinGene Products, revKaryopherinsNuclear ProteinsReceptors, Cytoplasmic and NuclearRNA, Messenger

Identifiers

PMID9405623
PMCPMC24994
OpenAlexW1968334377

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.