Evidence map›Paper›PMID 7760010›Full record

ArticleThe Journal of experimental medicine1995

Linkage of protection against amyloid fibril formation in the mouse to a single, autosomal dominant gene.

W A Gonnerman, R Elliott-Bryant, I Carreras, J D Sipe, E S Cathcart

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of experimental medicine, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. A concise review of amyloidosis in animals.Veterinary medicine international · 2012
    Article
  3. Protein folding pathology in domestic animals.Journal of Zhejiang University. Science · 2004
    Review
  4. Article
  5. 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 1 institution in 1 country.

W A GonnermanE. N. Rogers Memorial Veterans Affairs Hospital, Bedford, Massachusetts 01730, USA.
R Elliott-Bryant
I Carreras
J D Sipe
E S Cathcart
Edith Nourse Rogers Memorial Veterans Hospital · US

Funding

AMYLOID, AGING, AND DIETR01AG006860 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CATHCART, EDGAR S · 1987 to 1996
–
CELLULAR METABOLISM OF AMYLOID PROTEINS IN AGINGR01AG009006 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SCHREIBER, BARBARA M · 1990 to 1999
–
NIA NIH HHS AG06860NIA NIH HHS AG09006
6 · The paper itself

Abstract

Inbred strains of mice provide a model for studies of the pathogenesis of amyloid A (AA) amyloidosis. All susceptible strains of mice described to date codominantly express two serum amyloid A (apoSAA) isoforms, apoSAA1 and apoSAA2, of which only apoSAA2 serves as a precursor for amyloid fibrils. In previous studies, we have shown that the CE/J strain, which produces a single, novel apoSAA isoform, apoSAACE/J, is amyloid resistant. In the present study amyloid-resistant CE/J females were mated with amyloid-susceptible CBA/J males to produce F1 hybrid offspring which were then backcrossed to the parental CBA/J mouse strain. Amyloid susceptibility was determined in 30 backcrossed mice 72 h after injection of murine amyloid enhancing factor and silver nitrate. ApoSAA isoforms in plasma were separated by isoelectric focusing gel electrophoresis and visualized after immunoblotting with anti-AA antiserum. Amyloid A fibrils in spleen homogenates were denatured by formic acid and AA protein was quantified by ELISA using anti-mouse apoSAA antibodies. Values < 5 apoSAA equivalent units were considered negative. 13 mice expressed an apoSAA1 and apoSAA2 doublet characteristic of CBA/J mice, whereas 17 mice, expressed the apoSAACE/J isoform codominantly with apoSAA1 and apoSAA2. The correlation of amyloid resistance to expression of the apoSAACE/J isoform was absolute (17/17 were negative; mean score 2.6 +/- 0.17 [standard error of the mean] apoSAA equivalent units) and the correlation between amyloid susceptibility and the expression of apoSAA2/apoSAA1 was also striking (12/13 were amyloid positive; mean score 47.9 +/- 9.0 [standard error of the mean] apoSAA equivalent units (P < 0.001). This is not significantly different from the 50% segregation of apoSAA phenotypes expected for linkage to a single gene. These results indicate that a single gene governs apoSAACE/J expression and thus confers protection against amyloid deposition even in the presence of apoSAA1 and apoSAA2 isoforms and show for the first time that resistance to AA amyloidosis is a dominant trait governed by a single gene.

Indexed as

Genes, DominantGenetic LinkageAmino Acid SequenceAmyloidosisAnimalsCrosses, GeneticFemaleGene ExpressionGenetic Predisposition to DiseaseMaleMiceMice, Inbred CBAMice, Inbred StrainsMolecular Sequence DataSerum Amyloid A ProteinSpecies SpecificitySerum Amyloid A Protein

Identifiers

PMID7760010
PMCPMC2192067
OpenAlexW1992518762

What OpenQuestion holds

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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.