Evidence map›Paper›PMID 8013255›Full record

ArticleChromosoma1994

Mouse centromere mapping using oligonucleotide probes that detect variants of the minor satellite.

D Kipling, H E Wilson, A R Mitchell, B A Taylor, H J Cooke

Abstract read
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In one paragraph

Article in Chromosoma, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
8.5field-weighted citation impact, top 2% 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

29 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. LINE-related component of mouse heterochromatin and complex chromocenters' composition.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2016
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Centromere mitotic recombination in mammalian cells.The Journal of cell biology · 2008
    Article
  13. Article
  14. Article
  15. Characterization of a centromeric marker on mouse chromosome 11 and its introgression in a domesticus/musculus hybrid zone.Mammalian genome : official journal of the International Mammalian Genome Society · 2004
    Article
  16. Article
  17. Distinctive higher-order chromatin structure at mammalian centromeres.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Article
  18. Article
  19. Chromatin structure analysis of the mouse Xist locus.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  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

5 authors at 2 institutions in 2 countries.

D KiplingMRC Human Genetics Unit, Western General Hospital, Edinburgh, UK.
H E Wilson
A R Mitchell
B A Taylor
H J Cooke
Western General Hospital · GBJackson Laboratory · US

Funding

GENETIC ANALYSIS OF COMPLEX INFIRMITIESR01GM018684 · NIGMS · JACKSON LABORATORY · PI TAYLOR, BENJAMIN A · 1985 to 1996
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NIGMS NIH HHS GM18684
6 · The paper itself

Abstract

Cytologically, the centromere is found at the very end of most Mus musculus chromosomes, co-localizing with an array of minor satellite sequences. It is separated from the euchromatin of the long arm by a large domain of heterochromatin, composed in part of arrays of major satellite sequences. We used oligonucleotide probes that specifically detect regions of sequence variation found in certain cloned minor satellite sequences. They detect a limited subset of the minor satellite arrays in the mouse genome, based on both pulsed-field gel electrophoresis and in situ hybridization data, and provide direct molecular genetic markers for individual centromeres in some inbred mouse strains. Array size polymorphisms detected by these probes map to positions consistent with the centromeres of chromosomes 1 and 14 in the BXD recombinant inbred (RI) strains. The genetic distances between these minor satellite arrays and loci on the long arms of chromosomes 1 and 14 are consistent with repression of meiotic recombination in the heterochromatic domains separating them. The existence of chromosome-specific minor satellite sequences implies that the rate of sequence exchange between non-homologous chromosomes relative to the rate between homologous chromosomes is much lower than has previously been postulated. We suggest that the high degree of sequence homogeneity of mouse satellite sequences may instead reflect recent common ancestry.

Indexed as

Genetic VariationAnimalsBase SequenceCentromereChromosome MappingDNADNA, SatelliteMiceMice, Inbred C57BLMice, Inbred DBAMice, Inbred StrainsMolecular Sequence DataOligonucleotide ProbesDNADNA, SatelliteOligonucleotide Probes

Identifiers

PMID8013255
OpenAlexW2080416502

What OpenQuestion holds

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Read underepoch 390

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.