Evidence map›Paper›PMID 9751752›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1998

Trans-chromosomal recombination within the Ig heavy chain switch region in B lymphocytes.

M Kingzette, H Spieker-Polet, P C Yam, S K Zhai, K L Knight

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

15 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Double-stranded DNA break polarity skews repair pathway choice during intrachromosomal and interchromosomal recombination.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  5. Article
  6. Review
  7. Article
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  12. AID to overcome the limitations of genomic information by introducing somatic DNA alterations.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2006
    Review
  13. Article
  14. Article
  15. 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 2 institutions in 1 country.

M KingzetteDepartment of Microbiology and Immunology, Loyola University of Chicago, 2160 South First Avenue, Maywood, IL 60153, USA.
H Spieker-Polet
P C Yam
S K Zhai
K L Knight
University of Chicago · USLoyola University Chicago · US

Funding

GENETIC CONTROL OF IMMUNOGLOBULIN VARIABLE REGIONSR01AI016611 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KNIGHT, KATHERINE L · 1985 to 2002
$1.0M
STRUCTURE AND GENETIC CONTROL OF IGAR01AI011234 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KNIGHT, KATHERINE L · 1985 to 2000
$297k
Regulation of the Expression of Multiple IgA IsotypesR21AI011234 · NIAID · LOYOLA UNIVERSITY CHICAGO · PI KNIGHT, KATHERINE L · 2001 to 2001
$296k
STRUCTURE AND GENETIC CONTROL OF IGAR37AI011234 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KNIGHT, KATHERINE L · 1986 to 1995
–
NIAID NIH HHS AI11234NIAID NIH HHS AI16611
6 · The paper itself

Abstract

Somatic DNA rearrangements in B lymphocytes, including V(D)J gene rearrangements and isotype switching, generally occur in cis, i. e., intrachromosomally. We showed previously, however, that 3 to 7% of IgA heavy chains have the VH and Calpha regions encoded in trans. To determine whether the trans-association of VH and Calpha occurred by trans-chromosomal recombination, by trans-splicing, or by trans-chromosomal gene conversion, we generated and analyzed eight IgA-secreting rabbit hybridomas with trans-associated VH and Calpha heavy chains. By ELISA and by nucleotide sequence analysis we found that the VH and Calpha regions were encoded by genes that were in trans in the germline. We cloned the rearranged VDJ-Calpha gene from a fosmid library of one hybridoma and found that the expressed VH and Calpha genes were juxtaposed. Moreover, the juxtaposed VH and Calpha genes originated from different IgH alleles. From the same hybridoma, we also identified a fosmid clone with the other expected product of a trans-chromosomal recombination. The recombination breakpoint occurred within the Smicro/Salpha region, indicating that the trans-association of VH and Calpha genes occurred by trans-chromosomal recombination during isotype switching. We conclude that trans-chromosomal recombination occurs at an unexpectedly high frequency (7%) within the IgH locus of B lymphocytes in normal animals, which may explain the high incidence of B-cell tumors that arise from oncogene translocation into the IgH locus.

Indexed as

Gene Rearrangement, B-Lymphocyte, Heavy ChainRecombination, GeneticAllelesAnimalsBase SequenceB-LymphocytesCloning, MolecularDNA, ComplementaryDNA PrimersGene ExpressionGenes, ImmunoglobulinHybridomasImmunoglobulin AImmunoglobulin Switch RegionMolecular Sequence DataPhenotypeDNA, ComplementaryDNA PrimersImmunoglobulin A

Identifiers

PMID9751752
PMCPMC21727
OpenAlexW2132808863

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.