Evidence map›Paper›PMID 23161687›Full record

ArticleNucleic acids research2013

hnRNPL and nucleolin bind LINE-1 RNA and function as host factors to modulate retrotransposition.

Suresh Peddigari, Patrick Wai-Lun Li, Jennifer L Rabe, Sandra L Martin

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 74 citations in OpenAlex.

  1. LINE-1 Retrotransposons and Amyotrophic Lateral Sclerosis.International journal of molecular sciences · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. TheViruses · 2024
    Article
  6. Review
  7. Review
  8. Affinity-Based Interactome Analysis of Endogenous LINE-1 Macromolecules.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  9. Long non-coding RNAeLife · 2022
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
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

4 authors at 1 institution in 1 country.

Suresh PeddigariDepartment of Cell and Developmental Biology, University of Colorado School of Medicine, PO Box 6511, MS 8108, Aurora, CO 80045, USA. sandy.martin@ucdenver.edu
Patrick Wai-Lun Li
Jennifer L Rabe
Sandra L Martin
University of Colorado Denver · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Genetics &Biochemistry of a Murine RetroposonR01GM040367 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI MARTIN, SANDRA L · 1994 to 2009
$3.4M
NCI NIH HHS P30 CA046934NIGMS NIH HHS R01 GM40367
6 · The paper itself

Abstract

Long INterspersed Element one (LINE-1, or L1), is a widely distributed, autonomous retrotransposon in mammalian genomes. During retrotransposition, L1 RNA functions first as a dicistronic mRNA and then as a template for cDNA synthesis. Previously, we defined internal ribosome entry sequences (IRESs) upstream of both ORFs (ORF1 and ORF2) in the dicistronic mRNA encoded by mouse L1. Here, RNA affinity chromatography was used to isolate cellular proteins that bind these regions of L1 RNA. Four proteins, the heterogeneous nuclear ribonucleoproteins (hnRNPs) R, Q and L, and nucleolin (NCL), appeared to interact specifically with the ORF2 IRES. These were depleted from HeLa cells to examine their effects on L1 IRES-mediated translation and L1 retrotransposition. NCL knockdown specifically reduced the ORF2 IRES activity, L1 and L1-assisted Alu retrotransposition without altering L1 RNA or protein abundance. These findings are consistent with NCL acting as an IRES trans-acting factor (ITAF) for ORF2 translation and hence a positive host factor for L1 retrotransposition. In contrast, hnRNPL knockdown dramatically increased L1 retrotransposition as well as L1 RNA and ORF1 protein, indicating that this cellular protein normally interferes with retrotransposition. Thus, hnRNPL joins a small, but growing list of cellular proteins that are potent negative regulators of L1 retrotransposition.

Indexed as

Long Interspersed Nucleotide ElementsAnimalsBinding SitesEndonucleasesHeLa CellsHeterogeneous-Nuclear Ribonucleoprotein LHumansMiceNucleolinPhosphoproteinsProtein BiosynthesisRibonucleoproteinsRNARNA-Binding ProteinsRNA-Directed DNA PolymeraseRNA, Small InterferingECAT11 protein, mouseEndonucleasesHeterogeneous-Nuclear Ribonucleoprotein LL1 ORF1 protein, humanL1 ORF2 protein, humanNucleolinPhosphoproteinsRibonucleoproteinsRNARNA-Binding ProteinsRNA-Directed DNA PolymeraseRNA, Small Interfering

Identifiers

PMID23161687
PMCPMC3592465
OpenAlexW2158895446

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.