Evidence map›Paper›PMID 17339575›Full record

ArticleRNA (New York, N.Y.)2007

Probing the mRNA processing body using protein macroarrays and "autoantigenomics".

Wei-Hong Yang, Donald B Bloch

Open access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

48 citing papers in PubMed, 88 citations in OpenAlex.

  1. Y-box binding proteins in immunity and RNA virus infection.Microbiology and molecular biology reviews : MMBR · 2025
    Review
  2. Effects and Mechanisms of Imperatorin on Vitrified Mouse Oocytes.Animals : an open access journal from MDPI · 2025
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
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  11. Stress Granules and Processing Bodies in Translational Control.Cold Spring Harbor perspectives in biology · 2019
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Stress granules, P-bodies and cancer.Biochimica et biophysica acta · 2015
    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

2 authors at 1 institution in 1 country.

Wei-Hong YangCenter for Immunology and Inflammatory Diseases of the General Medical Services, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02129, USA.
Donald B Bloch
Harvard University · US

Funding

AUTOANTIGENS AND THE NUCLEAR BODYR29DK051179 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI BLOCH, DONALD B · 1996 to 2000
$121k
NIDDK NIH HHS DK051179
6 · The paper itself

Abstract

Messenger RNA processing bodies (P-bodies) are cellular structures that have a direct role in mRNA degradation. P-bodies have also been implicated in RNAi-mediated post-transcriptional gene silencing. Despite the important roles of P-bodies in cellular biology, the constituents of P-bodies and their organization have been only partially defined. Approximately 5% of patients with the autoimmune disease primary biliary cirrhosis have antibodies directed against these structures. Recent advances in protein macroarray technology permit the simultaneous screening of thousands of proteins for reactivity with autoantibodies. We used serum from patients with anti-P-body autoantibodies to screen a protein macroarray and identified 67 potential autoantigens. Immunoreactive proteins included four known P-body components and three additional primary biliary cirrhosis autoantigens. Y-box protein 1 (YB-1), a 50-kDa RNA-binding protein that was not previously known to be a P-body component, was recognized by serum from four of seven patients. YB-1 colocalized with P-body components DCP1a and Ge-1. In cells subjected to arsenite-induced oxidative stress, YB-1 localized to TIA-containing stress granules. Both YB-1 and the previously identified P-body component RAP55 translocated from P-bodies to stress granules during oxidative stress. During recovery, however, the reappearance of YB-1 in P-bodies was delayed compared with that of RAP55, suggesting that YB-1 and RAP55 may have different functions. This study demonstrates that the combination of human autoantibodies and protein macroarray technology provides a novel method for identifying and characterizing components of mRNA P-bodies.

Indexed as

RNA Processing, Post-TranscriptionalAnimalsArsenitesAutoantibodiesAutoantigensCells, CulturedCytoplasmic GranulesDNA-Binding ProteinsEndoribonucleasesHumansImmune SeraLiver Cirrhosis, BiliaryNuclear ProteinsOxidative StressPoly(A)-Binding ProteinsProtein Array AnalysisarseniteArsenitesAutoantibodiesAutoantigensDCP1A protein, humanDNA-Binding ProteinsEDC4 protein, humanEndoribonucleasesImmune SeraNuclear ProteinsPoly(A)-Binding ProteinsProteinsRibonucleoproteinsRNA-associated protein 55, humanRNA, MessengerT-Cell Intracellular Antigen-1TIA1 protein, humanTrans-ActivatorsY-Box-Binding Protein 1YBX1 protein, human

Identifiers

PMID17339575
PMCPMC1852818
OpenAlexW2107625090

What OpenQuestion holds

Textmetadata
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.