Evidence map›Paper›PMID 21324158›Full record

ArticleBMC genomics2011

Strain-specific copy number variation in the intelectin locus on the 129 mouse chromosome 1.

Zen H Lu, Alex di Domenico, Steven H Wright, Pamela A Knight, C Bruce A Whitelaw, Alan D Pemberton

Abstract read
In one paragraph

Article in BMC genomics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Human intelectin-2 (ITLN2) is selectively expressed by secretory Paneth cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  6. Characterization of an intelectin-1 (Frontiers in immunology · 2022
    Article
  7. Article
  8. Article
  9. Review
  10. 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

6 authors.

Zen H LuThe Roslin Institute and Royal (Dick) School of Veterinary Sciences, University of Edinburgh, Roslin, Midlothian, UK.
Alex di Domenico
Steven H Wright
Pamela A Knight
C Bruce A Whitelaw
Alan D Pemberton

Funding

Biotechnology and Biological Sciences Research Council BB/E009069Biotechnology and Biological Sciences Research Council BB/E009832/2Biotechnology and Biological Sciences Research Council BBS/E/D/05251442Biotechnology and Biological Sciences Research Council BBS/E/D/05251443Biotechnology and Biological Sciences Research Council BBS/E/D/05251444Biotechnology and Biological Sciences Research Council BBS/E/D/05251445Biotechnology and Biological Sciences Research Council BBS/E/R/00001613
6 · The paper itself

Abstract

backgroundC57BL/6J mice possess a single intelectin (Itln) gene on chromosome 1. The function of intelectins is not well understood, but roles have been postulated in insulin sensitivity, bacterial recognition, intestinal lactoferrin uptake and response to parasites and allergens. In contrast to C57BL/6J mice, there is evidence for expansion of the Itln locus in other strains and at least one additional mouse Itln gene product has been described. The aim of this study was to sequence and characterise the Itln locus in the 129S7 strain, to determine the nature of the chromosomal expansion and to inform possible future gene deletion strategies.

resultsSix 129S7 BAC clones were sequenced and assembled to generate 600 kbp of chromosomal sequence, including the entire Itln locus of approximately 500 kbp. The locus contained six distinct Itln genes, two CD244 genes and several Itln- and CD244-related pseudogenes. It was approximately 433 kbp larger than the corresponding C57BL/6J locus. The expansion of the Itln locus appears to have occurred through multiple duplications of a segment consisting of a full-length Itln gene, a CD244 (pseudo)gene and an Itln pseudogene fragment. Strong evidence for tissue-specific distribution of Itln variants was found, indicating that Itln duplication contributes more than a simple gene dosage effect.

conclusionsWe have characterised the Itln locus in 129S7 mice to reveal six Itln genes with distinct sequence and expression characteristics. Since C57BL/6J mice possess only a single Itln gene, this is likely to contribute to functional differences between C57BL/6J and other mouse strains.

Indexed as

Gene DosageGenetic LociAnimalsAntigens, CDBase SequenceBinding SitesChromosomes, Artificial, BacterialChromosomes, MammalianEvolution, MolecularGene LibraryGenomicsHomeodomain ProteinsLectinsMiceMice, 129 StrainMice, Inbred C57BLAntigens, CDCd244a protein, mouseHomeodomain ProteinsLectinsNkx3-1 protein, mouseReceptors, ImmunologicSignaling Lymphocytic Activation Molecule FamilyTranscription Factors

Identifiers

PMID21324158
PMCPMC3048546

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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.