Evidence map›Paper›PMID 17663983›Full record

ArticleAnalytical biochemistry2007

Detection of a rare oligo(A) repeat tract mutation (8As-->7As) in the sequence encoding the La/SS-B autoantigen.

Imre Semsei, Shannon Maier, Jennifer Workman-Azbill, László Urbán, Kathy Moser, Margit Zeher, Michael Bachmann, A Darise Farris

Open access · greenAbstract read
In one paragraph

Article in Analytical biochemistry, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 89% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

8 authors at 4 institutions in 3 countries.

Imre SemseiMolecular Biology Research Laboratory, 3rd Department of Medicine, Medical and Health Science Center, University of Debrecen, H-4004 Debrecen, Hungary. semsei@iiibel.dote.hu
Shannon Maier
Jennifer Workman-Azbill
László Urbán
Kathy Moser
Margit Zeher
Michael Bachmann
A Darise Farris
Oklahoma Medical Research Foundation · USUniversity of Debrecen · HUUniversity Hospital Carl Gustav Carus · DEUniversity of Minnesota · US

Funding

SNP Confirmation and High Throughput Genotyping CoreP30AR053483 · NIAMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI GUTHRIDGE, JOEL MARVIN · 2007 to 2017
$6.7M
THROMBOCYTOPENIA AND THE GENETICS OF SEVERE LUPUSP50AR048940 · NIAMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI REICHLIN, MORRIS · 2002 to 2006
$5.8M
Molecular Basis of Immunity - Kirschtein-NRSAT32AI007633 · NIAID · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI CUNNINGHAM, MADELEINE W. · 2001 to 2022
$4.0M
T cell to tolerance &autoimmunity to nuclear antigen LaR01AI048097 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI FARRIS, A DARISE · 2001 to 2012
$2.3M
Can Somatic Mutations Mediate Anti-La AutoimmunityR01GM063497 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI FARRIS, A. DARISE · 2002 to 2004
$776k
Tolerance to the Nuclear Antigen LaK02AI051647 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI FARRIS, A. DARISE · 2002 to 2006
$484k
NIAID NIH HHS K02 AI051647NIAID NIH HHS K02-AI051647NIAID NIH HHS R01 AI048097NIAID NIH HHS R01-AI048097NIAID NIH HHS T32 AI007633NIAMS NIH HHS P30 AR053483NIAMS NIH HHS P50 AR048940NIAMS NIH HHS P50-AR048940NIGMS NIH HHS R01 GM063497NIGMS NIH HHS R01-GM63497
6 · The paper itself

Abstract

Several diseases are characterized by the presence of point mutations, which are amenable to molecular detection using a number of methods such as PCR. However, certain mutations are particularly difficult to detect due to factors such as low abundance and the presence of special (e.g., oligonucleotide repeat) sequences. The mutation 7A in the oligoA sequence of exon 7 of the gene encoding the La autoantigen is difficult to detect at the DNA level, and even at the RNA level, due to both its estimated low abundance and its differentiation from the wild-type 8A sequence. This article describes a technique in which amplification of the excess wild-type 8A La sequence is suppressed by a peptide nucleic acid (PNA) during a nested PCR step. Detection of the amplified 7A mutant form was then performed by simple electrophoresis following a final primer extension step with an infrared dye-labeled primer. This technique allowed us to detect the mutation in 3 of 7 individuals harboring serum immunoglobulin G (IgG) antibodies reactive with a neo-B cell epitope in the 7A mutant protein product. We propose that this method is a viable screening test for mutations in regions containing simple polynucleotide repeats.

Indexed as

MutationSequence Analysis, DNAAutoantibodiesAutoantigensBase SequenceEpitopes, B-LymphocyteFemaleHumansImmunoglobulin GMaleMolecular Sequence DataOligodeoxyribonucleotidesPeptide Nucleic AcidsPolymerase Chain ReactionRepetitive Sequences, Nucleic AcidRibonucleoproteinsAutoantibodiesAutoantigensEpitopes, B-LymphocyteImmunoglobulin Goligodeoxyadenylic acidOligodeoxyribonucleotidesPeptide Nucleic AcidsRibonucleoproteinsSS-B Antigen

Identifiers

PMID17663983
PMCPMC2597489
OpenAlexW2045594827

What OpenQuestion holds

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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.