Evidence map›Paper›PMID 32267917›Full record

ArticleEndocrinology2020

Ins1-Cre and Ins1-CreER Gene Replacement Alleles Are Susceptible To Silencing By DNA Hypermethylation.

Elham Mosleh, Kristy Ou, Matthew W Haemmerle, Teguru Tembo, Andrew Yuhas, Bethany A Carboneau, Shannon E Townsend, Karin J Bosma, Maureen Gannon, Richard M O'Brien and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
13.5field-weighted citation impact, top 1% 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

15 citing papers in PubMed, 73 citations in OpenAlex.

  1. FOXM1 cooperates with ERα to regulate functional β-cell mass.American journal of physiology. Endocrinology and metabolism · 2025
    Article
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  11. β Cell GHS-R Regulates Insulin Secretion and Sensitivity.International journal of molecular sciences · 2021
    Article
  12. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Elham MoslehDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Kristy OuDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Matthew W HaemmerleInstitute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Teguru TemboDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Andrew YuhasDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Bethany A CarboneauDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee.
Shannon E TownsendDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee.
Karin J BosmaDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee.
Maureen GannonDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee.
Richard M O'BrienDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, Tennessee.
Doris A StoffersInstitute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Maria L GolsonDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
University of Pennsylvania · USVanderbilt University · USJohns Hopkins University · US

Funding

MULTIDISCIPLINARY TRAINING IN MOLECULAR ENDOCRINOLOGYT32DK007563 · NIDDK · VANDERBILT UNIVERSITY · PI Richard M O'Brien · 1988 to 2026
$15.9M
A stress inducible Pdx1 transcriptional complex governing beta cell survivalR01DK121175 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI STOFFERS, DORIS A · 2019 to 2023
$2.3M
Formation and maturation of endocrine pancreas progenitorsR01DK105689 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI GANNON, MAUREEN A, STOFFERS, DORIS A · 2016 to 2019
$2.2M
RESEARCH REGULATION OF MATURE BETA CELL FUNCTION BY THE TRANSCRIPTION FACTOR FOXM1R01DK110183 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI GOLSON, MARIA L · 2017 to 2021
$1.8M
Role of the RNA-binding, polyC-binding proteins in pancreatic beta cellsR01DK122039 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI STOFFERS, DORIS A · 2019 to 2022
$1.8M
Manipulating islet GPCR activity to promote beta cell proliferation and survivalR01DK120626 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GANNON, MAUREEN A · 2019 to 2022
$1.7M
Analysis of the Role of Post-Transcriptional Regulation by the Poly(C) Binding Proteins in Pancreatic Beta Cell HomeostasisF31DK117577 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI HAEMMERLE, MATTHEW · 2019 to 2021
$111k
Pathways regulating adult pancreatic beta cell replicationI01BX003744 · VA · VETERANS HEALTH ADMINISTRATION · PI GANNON, MAUREEN A · 2017 to 2020
–
BLRD VA I01 BX003744NIDDK NIH HHS F31 DK117577NIDDK NIH HHS R01 DK105689NIDDK NIH HHS R01 DK110183NIDDK NIH HHS R01 DK120626NIDDK NIH HHS R01 DK121175NIDDK NIH HHS R01 DK122039NIDDK NIH HHS T32 DK007563
6 · The paper itself

Abstract

Targeted gene ablation studies of the endocrine pancreas have long suffered from suboptimal Cre deleter strains. In many cases, Cre lines purportedly specific for beta cells also displayed expression in other islet endocrine cells or in a subset of neurons in the brain. Several pancreas and endocrine Cre lines have experienced silencing or mosaicism over time. In addition, many Cre transgenic constructs were designed to include the hGH mini-gene, which by itself increases beta-cell replication and decreases beta-cell function. More recently, driver lines with Cre or CreER inserted into the Ins1 locus were generated, with the intent of producing β cell-specific Cre lines with faithful recapitulation of insulin expression. These lines were bred in multiple labs to several different mouse lines harboring various lox alleles. In our hands, the ability of the Ins1-Cre and Ins1-CreER lines to delete target genes varied from that originally reported, with both alleles displaying low levels of expression, increased levels of methylation compared to the wild-type allele, and ultimately inefficient or absent target deletion. Thus, caution is warranted in the interpretation of results obtained with these genetic tools, and Cre expression and activity should be monitored regularly when using these lines.

Indexed as

AllelesAnimalsCells, CulturedDNA MethylationFemaleGene SilencingHEK293 CellsHumansInsulinInsulin-Secreting CellsIntegrasesIslets of LangerhansMaleMiceMice, Inbred C57BLMice, TransgenicCre recombinaseIns1 protein, mouseInsulinIntegrasesbeta cellsisletsmouse models

Identifiers

PMID32267917
PMCPMC7354059
OpenAlexW3014465926

What Socratic 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 Socratic graph.