Evidence map›Paper›PMID 10467404›Full record

ArticleOncogene1999

Transcriptional regulation by targeted recruitment of cyclin-dependent CDK9 kinase in vivo.

B Majello, G Napolitano, A Giordano, L Lania

Abstract read
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In one paragraph

Article in Oncogene, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

32 citing papers in PubMed, 64 citations in OpenAlex.

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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

4 authors at 3 institutions in 2 countries.

B MajelloDepartment of Genetics, Molecular and General Biology, University of Naples 'Federico II' and International Institute of Genetics and Biophysics, CNR, Naples, Italy.
G Napolitano
A Giordano
L Lania
University of Naples Federico II · ITInstitute of Genetics and Biophysics · ITJefferson Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CDK9 kinase in association with Cyclin T is a component of the transcription positive-acting complex pTEFb which facilitates the transition from abortive to productive transcription elongation by phosphorylating the carboxyl-terminal domain of RNA polymerase II. The Cyclin T1/CDK9 complex is implicated in Tat transactivation, and it has been suggested that Tat functions by recruiting this complex to RNAPII through cooperative binding to RNA. Here, we demonstrate that targeted recruitment of Cyclin T1/CDK9 kinase complex to specific promoters, through fusion to a DNA-binding domain of either Cyclin T1 or CDK9 kinase, stimulates transcription in vivo. Transcriptional enhancement was dependent on active CDK9, as a catalytically inactive form had no transcriptional effect. We determined that, unlike conventional activators, DNA-bound CDK9 does not activate enhancerless TATA-promoters unless TBP is overexpressed, suggesting that CDK9 acts in vivo at a step subsequent to TFIID recruitment DNA-bound. Finally, we determined that CDK9-mediated transcriptional activation is mediated by preferentially stimulating productive transcription elongation.

Indexed as

Gene Expression RegulationSaccharomyces cerevisiae ProteinsTranscription, GeneticCell Line, TransformedCyclin-Dependent Kinase 9Cyclin-Dependent KinasesCyclinsCyclin TDNA-Binding ProteinsFungal ProteinsHeLa CellsHIVHumansPromoter Regions, GeneticProto-Oncogene Proteins c-mycRecombinant Fusion ProteinsCCNT1 protein, humanCDK9 protein, humanCyclin-Dependent Kinase 9Cyclin-Dependent KinasesCyclinsCyclin TDNA-Binding ProteinsFungal ProteinsGAL4 protein, S cerevisiaeProto-Oncogene Proteins c-mycRecombinant Fusion ProteinsSaccharomyces cerevisiae ProteinsTATA-Box Binding ProteinTranscription Factors

Identifiers

PMID10467404
OpenAlexW2313475712

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.