Evidence map›Paper›PMID 29466324›Full record

ArticleNature2018

Sequences enriched in Alu repeats drive nuclear localization of long RNAs in human cells.

Yoav Lubelsky, Igor Ulitsky

Abstract read
In one paragraph

Article in Nature, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 202 papers.

0numbers the graph read from it
0cells of the map it votes in
202citing papers in PubMed
16.4field-weighted citation impact, top 1% 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

202 citing papers in PubMed, 358 citations in OpenAlex.

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  8. Robust mammalian RNA localization elements are complex and multipartite.bioRxiv : the preprint server for biology · 2026
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  14. eLife · 2026
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  17. High-throughput Screening of Sequence Elements Associated with RNA Localization.Computational and structural biotechnology journal · 2026
    Article
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142 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Yoav LubelskyDepartment of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel.
Igor UlitskyDepartment of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel.
Weizmann Institute of Science · IL

Funding

European Research Council 637878
6 · The paper itself

Abstract

Long noncoding RNAs (lncRNAs) are emerging as key parts of multiple cellular pathways, but their modes of action and how these are dictated by sequence remain unclear. lncRNAs tend to be enriched in the nuclear fraction, whereas most mRNAs are overtly cytoplasmic, although several studies have found that hundreds of mRNAs in various cell types are retained in the nucleus. It is thus conceivable that some mechanisms that promote nuclear enrichment are shared between lncRNAs and mRNAs. Here, to identify elements in lncRNAs and mRNAs that can force nuclear localization, we screened libraries of short fragments tiled across nuclear RNAs, which were cloned into the untranslated regions of an efficiently exported mRNA. The screen identified a short sequence derived from Alu elements and bound by HNRNPK that increased nuclear accumulation. Binding of HNRNPK to C-rich motifs outside Alu elements is also associated with nuclear enrichment in both lncRNAs and mRNAs, and this mechanism is conserved across species. Our results thus identify a pathway for regulation of RNA accumulation and subcellular localization that has been co-opted to regulate the fate of transcripts with integrated Alu elements.

Indexed as

RNA TransportActive Transport, Cell NucleusAlu ElementsAnimalsBase SequenceBinding SitesCell NucleusConserved SequenceEvolution, MolecularHeLa CellsHeterogeneous-Nuclear Ribonucleoprotein KHumansMCF-7 CellsMiceRNA, Long NoncodingRNA, MessengerHeterogeneous-Nuclear Ribonucleoprotein KHNRNPK protein, humanRNA, Long NoncodingRNA, MessengerUntranslated Regions

Identifiers

PMID29466324
PMCPMC6047738
OpenAlexW2754846502

What OpenQuestion holds

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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.