Evidence map›Paper›PMID 2120037›Full record

ArticleThe EMBO journal1990

A novel upstream element compensates for an ineffectual octamer motif in an immunoglobulin V kappa promoter.

M L Atchison, V Delmas, R P Perry

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The EMBO journal, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
5.3field-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

19 citing papers in PubMed, 48 citations in OpenAlex.

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  11. A mammalian DNA-binding protein that contains a chromodomain and an SNF2/SWI2-like helicase domain.Proceedings of the National Academy of Sciences of the United States of America · 1993
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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.

M L AtchisonFox Chase Cancer Center, Philadelphia, PA 19111.
V Delmas
R P Perry
Fox Chase Cancer Center · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI CHARNITA M. ZEIGLER-JOHNSON · 1985 to 2026
$138.8M
STUDIES OF IMMUNOGLOBULIN &RIBOSOMAL PROTEIN GENESR01AI017330 · NIAID · INSTITUTE FOR CANCER RESEARCH · PI PERRY, ROBERT P · 1985 to 1995
–
NCI NIH HHS CA-06927NCRR NIH HHS RR-05539NIAID NIH HHS AI-17330
6 · The paper itself

Abstract

The octamer (or dc/cd) motif is considered to be a critical component of all immunoglobulin (Ig) promoters. Although the sequence of this motif is highly conserved among most Ig promoters, there are some notable examples in which efficiently expressed Ig genes contain divergent octamers with base substitutions that are demonstrably deleterious when tested with heterologous proximal promoter elements. To elucidate the mechanisms that enable these naturally occurring Ig genes to cope with divergent octamers, we analyzed two such promoters with regard to their ability to interact with relevant transcription factors. We found that the divergent octamer in the kappa O germline promoter strongly binds both Oct-1 and Oct-2 factors, presumably because of compensatory contributions by flanking DNA sequences. A more surprising result was obtained with the V kappa 19 promoter. In this case, the divergent octamer is a very weak Oct factor binding site and, without help from another upstream element, is inadequate for efficient promoter function. This additional element, termed kappa Y because of its high pyrimidine content (CTTCCTTA), serves as a binding site for a novel lymphoid-specific factor. When the divergent V kappa 19 octamer was converted to a strong Oct factor binding site by a single point mutation, the need for kappa Y was obviated. Interestingly, VH promoters that contain the same divergent octamer also contain an upstream element that is very similar to kappa Y.

Indexed as

Genes, ImmunoglobulinPromoter Regions, GeneticTranscription FactorsAnimalsBase SequenceB-LymphocytesCell LineDNA-Binding ProteinsHumansImmunoglobulin kappa-ChainsImmunoglobulin Variable RegionMiceMolecular Sequence DataMultigene FamilyMutagenesis, Site-DirectedNuclear ProteinsDNA-Binding ProteinsImmunoglobulin kappa-ChainsImmunoglobulin Variable RegionNuclear ProteinsOctamer Transcription Factor-2Oligonucleotide ProbesPOU2F2 protein, humanPou2f2 protein, mouseTranscription Factors

Identifiers

PMID2120037
PMCPMC552038
OpenAlexW1472803246

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.