Evidence map›Paper›PMID 8349828›Full record

ArticleThe Journal of clinical investigation1993

Immunochemical and molecular characterization of anti-RNA polymerase I autoantibodies produced by tight skin mouse.

S Shibata, T Muryoi, Y Saitoh, T D Brumeanu, C A Bona, K N Kasturi

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In one paragraph

Article in The Journal of clinical investigation, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

4 citing papers in PubMed, 33 citations in OpenAlex.

  1. Mouse Models of Skin Fibrosis.Methods in molecular biology (Clifton, N.J.) · 2021
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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 at 1 institution in 1 country.

S ShibataDepartment of Microbiology, Mount Sinai School of Medicine, New York 10029-6574.
T Muryoi
Y Saitoh
T D Brumeanu
C A Bona
K N Kasturi
Icahn School of Medicine at Mount Sinai · US

Funding

V REGION GENES ENCODING AUTOANTIBODIES--MOLECULAR AND PHENOTYPIC CHARACTERSITICSP01AI024671 · NIAID · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI MAYER, LLOYD F · 1988 to 2002
$2.6M
NIAID NIH HHS 1901-AI-24671
6 · The paper itself

Abstract

Autoantibodies against nuclear proteins like RNA polymerase I (RNA pol I) are produced in a number of rheumatic autoimmune diseases. Production of antibodies specific for the 190-kD subunit of RNA pol I appears to be characteristic in the patients with systemic sclerosis. Previous investigations have shown that the tight skin (TSK) mouse is an experimental model for systemic sclerosis. In the present study we show that the TSK mice produce high titers of anti-RNA pol I antibodies, both of IgM and IgG classes. To characterize the immunochemical properties of these antibodies we obtained a large panel of hybridomas from these mice. Analysis of these hybridomas revealed that clonal frequency of autoreactive B cells specific for RNA pol I are higher in the TSK mice that in the controls. mAbs obtained from the TSK mice were specific for the 190-kD subunit and cross-reacted with Escherichia coli and phage T7 RNA polymerases (155-, 150-, and 107-kD polypeptides). We have also demonstrated that these antibodies bind better to the phosphorylated enzymes. The anti-RNA pol I mAbs were divided into three groups in terms of their functional property. The first group of antibodies increased the catalytic activity of the enzyme whereas the antibodies of the second group inhibited the enzymatic activity. Competitive inhibition RIAs showed that these two groups of antibodies bound to distinct epitopes. The third group of antibodies was neutral and had no activity on the enzyme function. These results suggest that TSK mouse anti-RNA pol I antibodies recognize three or more conserved epitopes. To understand the molecular basis of the generation of such autoreactive antibodies we analyzed their V gene repertoire. Northern analysis of RNAs of 14 TSK hybridomas showed that the VH genes encoding these antibodies were mainly from VH J558 family. It is possible that these genes were derived from a single germline gene or from a set of related genes of a single subgroup.

Indexed as

Genes, ImmunoglobulinAnimalsAntibodies, MonoclonalAutoantibodiesBacteriophage T7Binding, CompetitiveBlotting, WesternCross ReactionsEscherichia coliFluorescent Antibody TechniqueHybridomasImmunoglobulin Heavy ChainsKineticsLymphocytesMiceMice, Inbred C57BLAntibodies, MonoclonalAutoantibodiesImmunoglobulin Heavy ChainsRNA Polymerase I

Identifiers

PMID8349828
PMCPMC294939
OpenAlexW1973662600

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.