Evidence map›Paper›PMID 7984409›Full record

ArticleNucleic acids research1994

Identification of a 59 bp enhancer located at the first exon/intron boundary of the human O6-methylguanine DNA methyltransferase gene.

L C Harris, J S Remack, T P Brent

Open access · bronzeAbstract read
In one paragraph

Article in Nucleic acids research, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

22 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
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  3. Association betweenCells · 2023
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  5. Genomic Space ofInternational journal of molecular sciences · 2021
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  8. MRI to MGMT: predicting methylation status in glioblastoma patients using convolutional recurrent neural networks.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2018
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  15. The A/G allele of rs16906252 predicts for MGMT methylation and is selectively silenced in premalignant lesions from smokers and in lung adenocarcinomas.Clinical cancer research : an official journal of the American Association for Cancer Research · 2011
    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.

L C HarrisDepartment of Molecular Pharmacology, St Jude Children's Research Hospital, Memphis, TN 38101-0318.
J S Remack
T P Brent
St. Jude Children's Research Hospital · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SUZANNE J. BAKER · 1985 to 2026
$166.9M
ENZYMES AND REACTIONS FOR REPAIR OF DNA IN HUMAN CELLSR01CA014799 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI HARRIS, LINDA C · 1985 to 2003
$1.1M
NCI NIH HHS CA 14799NCI NIH HHS P30 CA 21765
6 · The paper itself

Abstract

The DNA repair enzyme, O6-methylguanine DNA methyltransferase (MGMT) is responsible for repair of damage induced by alkylating agents that produce adducts at O6-guanine in DNA. Although the MGMT gene promoter has housekeeping gene promoter characteristics, unlike these genes which are expressed at a constant level, MGMT transcriptional activity varies between cell types. During an attempt to identify regions of the MGMT regulatory sequence sensitive to variations in transcription factors between cell types, we have identified a 59 bp enhancer which is required for efficient MGMT promoter function. This fragment produced increased transcriptional activity in reporter gene constructs containing either the MGMT or UMP-synthase promoter when transfected into either of two cell lines; it seems therefore that this enhancer may interact with relatively common trans-acting factors. Functional activity is only detected when the enhancer is in 'cis' with respect to the promoter, suggesting that complexes are formed between proteins bound to the enhancer and promoter sequences. We propose that the enhancer-binding protein may be a novel transcription factor since there are no obvious consensus sequences within the 59 bp sequence for known DNA-binding proteins.

Indexed as

Base SequenceCell LineDNADNA-Binding ProteinsEnhancer Elements, GeneticExonsHumansIntronsMethyltransferasesMolecular Sequence DataMultienzyme ComplexesO(6)-Methylguanine-DNA MethyltransferaseOrotate PhosphoribosyltransferaseOrotidine-5'-Phosphate DecarboxylasePromoter Regions, GeneticT-LymphocytesDNADNA-Binding ProteinsMethyltransferasesMultienzyme ComplexesO(6)-Methylguanine-DNA MethyltransferaseOrotate PhosphoribosyltransferaseOrotidine-5'-Phosphate Decarboxylaseuridine 5'-monophosphate synthase

Identifiers

PMID7984409
PMCPMC308508
OpenAlexW2026770360

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.