Evidence map›Paper›PMID 12096188›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2002

dELL is an essential RNA polymerase II elongation factor with a general role in development.

Joel C Eissenberg, Jiyan Ma, Mark A Gerber, Alan Christensen, James A Kennison, Ali Shilatifard

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

35 citing papers in PubMed, 75 citations in OpenAlex.

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  16. RNA polymerase II elongation control.Annual review of biochemistry · 2012
    Review
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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

6 authors at 3 institutions in 1 country.

Joel C EissenbergEdward A. Doisy Department of Biochemistry and Molecular Biology, St. Louis University School of Medicine, 1402 South Grand Boulevard, St. Louis, MO 63104, USA. eissenjc@slu.edu
Jiyan Ma
Mark A Gerber
Alan Christensen
James A Kennison
Ali Shilatifard
Eunice Kennedy Shriver National Institute of Child Health and Human Development · USUniversity of Nebraska–Lincoln · USNational Institutes of Health · US

Funding

Regulation Of Cellular Proliferation And Diversity In DrosophilaZIAHD001005 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI KENNISON, JAMES A. · 2009 to 2019
$8.1M
Physiological Role of MLL and ELL Proteins in LeukemiaR01CA089455 · NCI · STOWERS INSTITUTE FOR MEDICAL RESEARCH · PI SHILATIFARD, ALI · 2001 to 2015
$3.5M
REGULATION OF CELLULAR PROLIFERATION AND DIVERSITY IN DROSOPHILAZ01HD001005 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI KENNISON, JAMES A. · 1988 to 2008
$1.4M
MECHANISM OF EPIGENETIC REGULATION IN DROSOPHILAR55GM057005 · NIGMS · SAINT LOUIS UNIVERSITY · PI EISSENBERG, JOEL C · 1998 to 1998
–
NCI NIH HHS 1R01CA089455NCI NIH HHS R01 CA089455NIGMS NIH HHS 1R55GM057005
6 · The paper itself

Abstract

Several eukaryotic proteins increase RNA polymerase II (Pol II) transcription rates in vitro. The relative contributions of these factors to gene expression in vivo is unknown. The ELL family of proteins promote Pol II elongation in vitro, and the Drosophila ELL homolog (dELL) is associated with Pol II at sites of transcription in vivo. The purpose of this study was to test whether an ELL family protein is required for gene expression in vivo. We show that dELL is encoded by the Suppressor of Triplo-lethal locus [Su(Tpl)]. We have characterized seven distinct mutant alleles of Su(Tpl) and show that a dELL transgene rescues recessive lethality of Su(Tpl). Su(Tpl) mutations cause abnormal embryonic segmentation and dominantly modify expression of diverse genes during development. These data show that an ELL family elongation factor is essential, acts broadly in development, and is not functionally redundant to other elongation factors in vivo.

Indexed as

Amino Acid SequenceAnimalsCrosses, GeneticDNA-Binding ProteinsDrosophilaDrosophila ProteinsEmbryo, NonmammalianEthyl MethanesulfonateFemaleGene Expression Regulation, DevelopmentalGenotypeMaleMolecular Sequence DataMorphogenesisMutagenesisPeptide Elongation FactorsDNA-Binding ProteinsDrosophila ProteinsEthyl MethanesulfonatePeptide Elongation FactorsRecombinant ProteinsRNA Polymerase IISu(Tpl) protein, DrosophilaTranscription Factors

Identifiers

PMID12096188
PMCPMC125055
OpenAlexW2046090066

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.