Evidence map›Paper›PMID 22355610›Full record

ArticleScientific reports2011

Specific Y14 domains mediate its nucleo-cytoplasmic shuttling and association with spliced mRNA.

Naoyuki Kataoka, Michael D Diem, Mayumi Yoshida, Chihiro Hatai, Izumi Dobashi, Gideon Dreyfuss, Masatoshi Hagiwara, Mutsuhito Ohno

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. 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

8 authors at 3 institutions in 2 countries.

Naoyuki KataokaMedical Top Track Program, Medical Research Institute, Tokyo Dental and Medical University, Tokyo 113-8510, Japan. kataoka.naoyuki.6m@kyoto-u.ac.jp
Michael D Diem
Mayumi Yoshida
Chihiro Hatai
Izumi Dobashi
Gideon Dreyfuss
Masatoshi Hagiwara
Mutsuhito Ohno
Kyoto University · JPTokyo Medical and Dental University · JPHoward Hughes Medical Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pre-mRNA splicing deposits multi-protein complexes, termed exon junction complexes (EJCs), on mRNAs near exon-exon junctions. The core of EJC consists of four proteins, eIF4AIII, MLN51, Y14 and Magoh. Y14 is a nuclear protein that can shuttle between the nucleus and the cytoplasm, and binds specifically to Magoh. Here we delineate a Y14 nuclear localization signal that also confers its nuclear export, which we name YNS. We further identified a 12-amino-acid peptide near Y14's carboxyl terminus that is required for its association with spliced mRNAs, as well as for Magoh binding. Furthermore, the Y14 mutants, which are deficient in binding to Magoh, could still be localized to the nucleus, suggesting the existence of both the nuclear import pathway and function for Y14 unaccompanied by Magoh.

Indexed as

RNA SplicingAmino Acid SequenceCell NucleusCytoplasmExonsHeLa CellsHumansMolecular Sequence DataNuclear Export SignalsProtein TransportRNA-Binding ProteinsRNA, MessengerNuclear Export SignalsRBM8A protein, humanRNA-Binding ProteinsRNA, Messenger

Identifiers

PMID22355610
PMCPMC3216578
OpenAlexW1973296733

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.