Evidence map›Paper›PMID 10430927›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1999

A silencer element identified in Drosophila is required for imprinting of H19 reporter transgenes in mice.

J D Brenton, R A Drewell, S Viville, K J Hilton, S C Barton, J F Ainscough, M A Surani

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Analysis of imprinted murine Peg3 locus in transgenic mice.Mammalian genome : official journal of the International Mammalian Genome Society · 2004
    Article
  9. Article
  10. Article
  11. Article
  12. Regulatory mechanisms at the mouse Igf2/H19 locus.Molecular and cellular biology · 2001
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
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

7 authors.

J D BrentonWellcome/Cancer Research Campaign Institute of Cancer and Developmental Biology and Physiological Laboratory, University of Cambridge, Tennis Court Road, Cambridge, CB2 1QR, United Kingdom.
R A Drewell
S Viville
K J Hilton
S C Barton
J F Ainscough
M A Surani

Funding

Wellcome Trust
6 · The paper itself

Abstract

The H19 gene is subject to genomic imprinting because it is methylated and repressed after paternal inheritance and is unmethylated and expressed after maternal inheritance. We recently identified a 1.1-kb control element in the upstream region of the H19 gene that functions as a cis-acting silencer element in Drosophila. Here we investigate the function of this element in mice. We demonstrate that both H19-lacZ and H19-PLAP reporter transgenes can undergo imprinting with repression and hypermethylation after paternal transmission at many integration sites. However, transgenes that were deleted for the 1.1-kb silencer element showed loss of paternal repression, but they did not show marked changes in the paternal methylation of the remaining upstream region. This study demonstrates that the 1.1-kb control element identified in Drosophila is required to silence paternally transmitted H19 minitransgenes in mice.

Indexed as

Genes, Tumor SuppressorGenomic ImprintingRNA, UntranslatedAlkaline PhosphataseAnimalsbeta-GalactosidaseChromosome MappingDNA MethylationDrosophilaFemaleGene LibraryGenes, ReporterGenetic TechniquesIsoenzymesMaleMiceAlkaline Phosphatasebeta-Galactosidasegerm-cell AP isoenzymeH19 long non-coding RNAIsoenzymesMuscle ProteinsRNA, Long NoncodingRNA, Untranslated

Identifiers

PMID10430927
PMCPMC17764

What OpenQuestion holds

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Registered trials

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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.