Evidence map›Paper›PMID 17327454›Full record

ArticleDiabetes2007

Glucose regulation of insulin gene transcription and pre-mRNA processing in human islets.

Carmella Evans-Molina, James C Garmey, Robert Ketchum, Kenneth L Brayman, Shaoping Deng, Raghavendra G Mirmira

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

54 citing papers in PubMed, 92 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

6 authors at 2 institutions in 1 country.

Carmella Evans-MolinaUniversity of Virginia Health System, 450 Ray C. Hunt Drive, Charlottesville, VA 22908, USA.
James C Garmey
Robert Ketchum
Kenneth L Brayman
Shaoping Deng
Raghavendra G Mirmira
University of Virginia · USUniversity of Pennsylvania · US

Funding

Transcriptional Mechanisms Governing Beta Cell DifferentiationR01DK060581 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Raghavendra G Mirmira · 2002 to 2026
$8.5M
PILOT--PILOT/FEASIBILITY PROGRAMP30DK063609 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI BARRETT, EUGENE JOSEPH · 2003 to 2007
$5.7M
Transcriptional Regulation of the Insulin Gene in Health and DiseaseK08DK080225 · NIDDK · UNIVERSITY OF VIRGINIA · PI EVANS-MOLINA, CARMELLA · 2007 to 2011
$701k
Epigenetic Changes in Type 2 Diabetes MellitusF32DK076450 · NIDDK · UNIVERSITY OF VIRGINIA · PI EVANS-MOLINA, CARMELLA EVANS · 2006 to 2007
$69k
NIDDK NIH HHS DK 063609NIDDK NIH HHS F32 DK076450NIDDK NIH HHS F32 DK 076450-01NIDDK NIH HHS K08 DK080225NIDDK NIH HHS P30 DK063609NIDDK NIH HHS R01 DK060581NIDDK NIH HHS R01 DK 60581NIDDK NIH HHS T32 DK 073202 5
6 · The paper itself

Abstract

Glucose is the primary regulator of insulin granule release from pancreatic islets. In rodent islets, the role of glucose in the acute regulation of insulin gene transcription has remained unclear, primarily because the abundance and long half-life of insulin mRNA confounds analysis of transcription by traditional methods that measure steady-state mRNA levels. To investigate the nature of glucose-regulated insulin gene transcription in human islets, we first quantitated the abundance and half-lives of insulin mRNA and pre-mRNAs after addition of actinomycin D (to stop transcription). Our results indicated that intron 1-and intron 2-containing pre-mRNAs were approximately 150- and 2,000-fold less abundant, respectively, than mature mRNA. 5' intron 2-containing pre-mRNAs displayed half-lives of only approximately 60 min, whereas all other transcripts displayed more extended lifetimes. In response to elevated glucose, pre-mRNA species increased within 60 min, whereas increases in mature mRNA did not occur until 48 h, suggesting that measurement of mature mRNA species does not accurately reflect the acute transcriptional response of the insulin gene to glucose. The acute increase in pre-mRNA species was preceded by a sixfold increase in histone H4 acetylation and a twofold increase in RNA polymerase II recruitment at the insulin promoter. Taken together, our data suggest that pre-mRNA species may be a more reliable reflection of acute changes to human insulin gene transcriptional rates and that glucose acutely enhances insulin transcription by a mechanism that enhances chromatin accessibility and leads to recruitment of basal transcriptional machinery.

Indexed as

GlucoseHumansInsulinIslets of LangerhansRNA, MessengerTranscription, GeneticGlucoseInsulinRNA, Messenger

Identifiers

PMID17327454
PMCPMC3705758
OpenAlexW2114742434

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.