Evidence map›Paper›PMID 31393940›Full record

ArticlePloS one2019

Characterization of a BAC transgenic mouse expressing Krt19-driven iCre recombinase in its digestive organs.

Tomohiro Kanayama, Hiroyuki Tomita, Nguyen Huy Binh, Yuichiro Hatano, Hitomi Aoki, Hideshi Okada, Akihiro Hirata, Yoshitaka Fujihara, Takahiro Kunisada, Akira Hara

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

10 authors at 3 institutions in 2 countries.

Tomohiro KanayamaDepartment of Tumor Pathology, Gifu University Graduate School of Medicine, Gifu, Japan.
Hiroyuki TomitaDepartment of Tumor Pathology, Gifu University Graduate School of Medicine, Gifu, Japan.ORCID 0000-0002-3291-0274
Nguyen Huy BinhDepartment of Tumor Pathology, Gifu University Graduate School of Medicine, Gifu, Japan.
Yuichiro HatanoDepartment of Tumor Pathology, Gifu University Graduate School of Medicine, Gifu, Japan.ORCID 0000-0002-5121-6325
Hitomi AokiDepartment of Tissue and Organ Development, Gifu University Graduate School of Medicine, Gifu, Japan.
Hideshi OkadaDepartment of Emergency and Disaster Medicine, Gifu University Graduate School of Medicine, Gifu, Japan.
Akihiro HirataDivision of Animal Experiment, Life Science Research Center, Gifu University, Gifu, Japan.
Yoshitaka FujiharaResearch Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.
Takahiro KunisadaDepartment of Tissue and Organ Development, Gifu University Graduate School of Medicine, Gifu, Japan.
Akira HaraDepartment of Tumor Pathology, Gifu University Graduate School of Medicine, Gifu, Japan.
Gifu University · JPHanoi Medical University · VNThe University of Osaka · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytokeratin 19 (KRT19) protein is highly expressed in the epithelium of the gastrointestinal (GI) tract, hepatobiliary tissues, and pancreas of humans and mice. In the present study, we used an improved Cre (iCre) gene to enhance the efficiency of Cre expression in mammalian cells. We established a new transgenic Krt19-iCre bacterial artificial chromosome (BAC) mouse model using the BAC recombineering strategy. Site-specific iCre expression pattern was examined in embryos, adults, and elderly Krt19-iCre mice crossed with Tomato or LacZ reporter mice. Both iCre and reporter protein expressions in adult Krt19-iCre;Tomatoflox/+ (Krt19-iCre Tomato reporter) mice were observed mainly in the epithelial cells of the GI tract, hepatobiliary tissues, and pancreas. However, the expression in the intrahepatic and small pancreatic duct were lower than those in the common bile and large pancreatic duct. In the Krt19-iCre; LacZ reporter embryos, β-galactosidase for the LacZ reporter was expressed in the glandular epithelial cells of the GI tract in 9.5-day embryos, 12-day embryos, and newborn mice. The reporter protein expression in Krt19-iCre-Tomato reporter mice was consistent with the KRT19 expression in human GI tissues. In conclusion, Krt19-iCre BAC transgenic mice can be used to investigate developmental and pathological conditions using the iCre-loxP system.

Indexed as

AnimalsChromosomes, Artificial, BacterialDigestive SystemGenes, ReporterIntegrasesKeratin-19Lac OperonMiceMice, TransgenicModels, AnimalCre recombinaseIntegrasesKeratin-19

Identifiers

PMID31393940
PMCPMC6687107
OpenAlexW2967623571

What OpenQuestion holds

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LicenceCC BY
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.