Evidence map›Paper›PMID 15870260›Full record

ArticleMolecular and cellular biology2005

Functional characterization of a novel Ku70/80 pause site at the H19/Igf2 imprinting control region.

David J Katz, Michael A Beer, John M Levorse, Shirley M Tilghman

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Long Noncoding RNANon-coding RNA · 2026
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  6. The Ku70 DNA-repair protein is involved in centromere function in a grasshopper species.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2013
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  11. The DNA-repair Ku70 protein is located in the nucleus and tail of elongating spermatids in grasshoppers.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2007
    Article
  12. DNA damage and L1 retrotransposition.Journal of biomedicine & biotechnology · 2006
    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.

David J KatzDepartment of Molecular Biology, One Nassau Hall, Princeton University, Princeton, NJ 08544-0015, USA.
Michael A Beer
John M Levorse
Shirley M Tilghman
Princeton University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The imprinted expression of the H19 and Igf2 genes in the mouse is controlled by an imprinting control center (ICR) whose activity is regulated by parent-of-origin differences in methylation. The only protein that has been implicated in ICR function is the zinc-finger protein CTCF, which binds at multiple sites within the maternally inherited ICR and is required to form a chromatin boundary that inhibits Igf2 expression. To identify other proteins that play a role in imprinting, we employed electrophoresis mobility shift assays to identify two novel binding sites within the ICR. The DNA binding activity was identified as the heterodimer Ku70/80, which binds nonspecifically to free DNA ends. The sites within the ICR bind Ku70/80 in a sequence-specific manner and with higher affinity than previously reported binding sites. The binding required the presence of Mg(2+), implying that the sequence is a pause site for Ku70/80 translocation from a free end. Chromatin immunoprecipitation assays were unable to confirm that Ku70/80 binds to the ICR in vivo. In addition, mutation of these binding sites in the mouse did not result in any imprinting defects. A genome scan revealed that the binding site is found in LINE-1 retrotransposons, suggesting a possible role for Ku70/80 in transposition.

Indexed as

AnimalsAntigens, NuclearBase SequenceBinding SitesDNADNA-Binding ProteinsFemaleGenomeGenomic ImprintingGenomicsInsulin-Like Growth Factor IIKu AutoantigenMaleMiceMultiprotein ComplexesMutationAntigens, NuclearDNADNA-Binding ProteinsH19 long non-coding RNAInsulin-Like Growth Factor IIKu AutoantigenMultiprotein ComplexesRNA, Long NoncodingRNA, UntranslatedXrcc6 protein, mouse

Identifiers

PMID15870260
PMCPMC1087736
OpenAlexW2149892710

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.