Evidence map›Paper›PMID 1628630›Full record

ArticleThe EMBO journal1992

Surface IgM mediated regulation of RAG gene expression in E mu-N-myc B cell lines.

A Ma, P Fisher, R Dildrop, E Oltz, G Rathbun, P Achacoso, A Stall, F W Alt

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 87 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. B cell receptor expression level determines the fate of developing B lymphocytes: receptor editing versus selection.Proceedings of the National Academy of Sciences of the United States of America · 2000
    Article
  6. Article
  7. Receptor selection in B and T lymphocytes.Annual review of immunology · 2000
    Review
  8. Article
  9. RAG2 is regulated differentially in B and T cells by elements 5' of the promoter.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  10. Induction of Ig light chain gene rearrangement in heavy chain-deficient B cells by activated Ras.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Receptor editing in self-reactive bone marrow B cells.The Journal of experimental medicine · 1993
    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

8 authors at 1 institution in 1 country.

A MaHoward Hughes Medical Institute, Boston, MA.
P Fisher
R Dildrop
E Oltz
G Rathbun
P Achacoso
A Stall
F W Alt
Howard Hughes Medical Institute · US

Funding

Mechanisms that Control IgH Variable Region Exon AssemblyR01AI020047 · NIAID · IMMUNE DISEASE INSTITUTE, INC. · PI ALT, FREDERICK W. · 1985 to 2025
$14.1M
THE DETERMINANTS OF MUTATIONP01CA023767 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI AXEL, RICHARD · 1985 to 2008
$8.3M
ASSEMBLY AND EXPRESSION OF IG VARIBLE REGION GENESR37AI020047 · NIAID · IMMUNE DISEASE INSTITUTE, INC. · PI ALT, FREDERICK W · 1991 to 2000
$323k
TRAINING IN MOLECULAR GENETICS AND GASTROENTEROLOGYK11DK001831 · NIDDK · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI MA, AVERIL I · 1988 to 1992
–
NCI NIH HHS CA 23767NIAID NIH HHS AI20047NIDDK NIH HHS DK01831
6 · The paper itself

Abstract

Transgenic mice carrying either the c-myc or N-myc oncogene deregulated by the immunoglobulin heavy chain enhancer element (E mu) develop both pre-B and B cell lymphomas (E mu-c-myc and E mu-N-myc lymphomas). We report here that B cell lines derived from these tumors, as well as a line derived from v-myc retroviral transformation, simultaneously express surface immunoglobulin (a hallmark of mature B cells) as well as a common subset of genes normally restricted to the pre-B stage of development-including the recombinase activating genes RAG-1 and RAG-2. Continued RAG-1 and RAG-2 expression in these lines is associated with VDJ recombinase activity detected with a VDJ recombination substrate. Cross-linking of the surface immunoglobulin on these lines with an anti-mu antibody leads to rapid, specific and reversible down-regulation of RAG-1 and RAG-2 gene expression. We also find that a small but significant percentage of normal surface immunoglobulin bearing bone marrow B cells express the RAG-1 gene. These findings are discussed in the context of their possible implications for the control of specific gene expression during the pre-B to B cell transition.

Indexed as

DNA-Binding ProteinsGene Expression RegulationGenes, mycHomeodomain ProteinsAnimalsBlotting, NorthernB-LymphocytesBone MarrowBone Marrow CellsCell Transformation, ViralDNA NucleotidyltransferasesDown-RegulationEnhancer Elements, GeneticImmunoglobulin MLymphoma, B-CellMiceDNA-Binding ProteinsDNA NucleotidyltransferasesHomeodomain ProteinsImmunoglobulin MProteinsRAG-1 proteinRag2 protein, mouseVDJ RecombinasesV(D)J recombination activating protein 2

Identifiers

PMID1628630
PMCPMC556748
OpenAlexW1236747056

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.