Evidence map›Paper›PMID 3133550›Full record

ArticleMolecular and cellular biology1988

Genes activated in the presence of an immunoglobulin enhancer or promoter are negatively regulated by a T-lymphoma cell line.

D M Zaller, H Yu, L A Eckhardt

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 1988. 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
3.9field-weighted citation impact, top 5% 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, 51 citations in OpenAlex.

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  14. Nucleotide-sequence-specific de novo methylation in a somatic murine cell line.Proceedings of the National Academy of Sciences of the United States of America · 1989
    Article
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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

3 authors at 1 institution in 1 country.

D M ZallerDepartment of Biological Sciences, Columbia University, New York, New York 10027.
H Yu
L A Eckhardt
Columbia University · US

Funding

MOLECULAR GENETICS OF LYMPHOCYTE DIFFERENTIATIONR01AI021578 · NIAID · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI ECKHARDT, LAUREL A · 1985 to 1989
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NIAID NIH HHS AI21578PHS HHS M0721609
6 · The paper itself

Abstract

The tissue-specific expression of immunoglobulin genes can be partially explained by a requirement for activating factors found only in B lymphocytes and their derivatives. However, loss of immunoglobulin expression upon fusion of an immunoglobulin-producing myeloma cell with a T lymphoma cell (BW5147) or fibroblast (L cell) suggests that negatively acting factors also play a role in the tissue specificity of immunoglobulin genes. Expression of a cloned immunoglobulin heavy-chain gene introduced into myeloma cells was suppressed after fusion of the myeloma transformants with BW5147. The presence of either the immunoglobulin heavy-chain enhancer or promoter conferred suppression, under similar conditions, upon a heterologous gene that is normally expressed in both B and T lymphocytes. These immunoglobulin heavy-chain gene control regions, or gene modifications induced by them, are subject to negative control by T-lymphocyte-derived factors.

Indexed as

Enhancer Elements, GeneticGene Expression RegulationGenes, ImmunoglobulinAnimalsCell FusionHybridomasImmunoglobulin Heavy ChainsLymphomaMiceMice, Inbred AKRMice, Inbred BALB CPromoter Regions, GeneticRecombinant ProteinsT-LymphocytesTumor Cells, CulturedImmunoglobulin Heavy ChainsRecombinant Proteins

Identifiers

PMID3133550
PMCPMC363371
OpenAlexW1786474017

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.