Generation and characterization of an inducible transgenic model for studying mouse esophageal biology

<p>Abstract</p> <p>Background</p> <p>To facilitate the <it>in vivo</it> study of esophageal (stem) cell biology in homeostasis and cancer, novel mouse models are necessary to elicit expression of candidate genes in a tissue-specific and inducible fashion. To...

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Main Authors: Roth Sabrina, Franken Patrick, Monkhorst Kim, Kong a San John, Fodde Riccardo
Format: Article
Language:English
Published: BMC 2012-06-01
Series:BMC Developmental Biology
Subjects:
Online Access:http://www.biomedcentral.com/1471-213X/12/18
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spelling doaj-9a813be0f85944e196f536b39f2cd7c82020-11-25T00:22:20ZengBMCBMC Developmental Biology1471-213X2012-06-011211810.1186/1471-213X-12-18Generation and characterization of an inducible transgenic model for studying mouse esophageal biologyRoth SabrinaFranken PatrickMonkhorst KimKong a San JohnFodde Riccardo<p>Abstract</p> <p>Background</p> <p>To facilitate the <it>in vivo</it> study of esophageal (stem) cell biology in homeostasis and cancer, novel mouse models are necessary to elicit expression of candidate genes in a tissue-specific and inducible fashion. To this aim, we developed and studied a mouse model to allow labeling of esophageal cells with the histone 2B-GFP (H2B-GFP) fusion protein.</p> <p>Results</p> <p>First, we generated a transgenic mouse model expressing the reverse tetracycline transactivator rtTA2-M2 under control of the promoter (ED-L2) of the Epstein-Barr virus (EBV) gene encoding the latent membrane protein-1 (<it>LMP-1</it>). The newly generated ED-L2-rtTA2-M2 (ED-L2-rtTA) mice were then bred with the previously developed tetO-HIST1H2BJ/GFP (tetO-H2B-GFP) model to assess inducibility and tissue-specificity. Expression of the H2B-GFP fusion protein was observed upon doxycycline induction but was restricted to the terminally differentiated cells above the basal cell layer. To achieve expression in the basal compartment of the esophagus, we subsequently employed a different transgenic model expressing the reverse transactivator rtTA2S-M2 under the control of the ubiquitous, methylation-free CpG island of the human hnRNPA2B1-CBX3 gene (hnRNP-rtTA). Upon doxycycline administration to the compound hnRNP-rtTA/tetO-H2B-GFP mice, near-complete labeling of all esophageal cells was achieved. Pulse-chase experiments confirmed that complete turnover of the esophageal epithelium in the adult mouse is achieved within 7–10 days.</p> <p>Conclusions</p> <p>We show that the esophagus-specific promoter ED-L2 is expressed only in the differentiated cells above the basal layer. Moreover, we confirmed that esophageal turn-over in the adult mouse does not exceed 7–10 days.</p> http://www.biomedcentral.com/1471-213X/12/18MouseEsophagusTurnover ratePromoterED-L2Doxycycline inducible
collection DOAJ
language English
format Article
sources DOAJ
author Roth Sabrina
Franken Patrick
Monkhorst Kim
Kong a San John
Fodde Riccardo
spellingShingle Roth Sabrina
Franken Patrick
Monkhorst Kim
Kong a San John
Fodde Riccardo
Generation and characterization of an inducible transgenic model for studying mouse esophageal biology
BMC Developmental Biology
Mouse
Esophagus
Turnover rate
Promoter
ED-L2
Doxycycline inducible
author_facet Roth Sabrina
Franken Patrick
Monkhorst Kim
Kong a San John
Fodde Riccardo
author_sort Roth Sabrina
title Generation and characterization of an inducible transgenic model for studying mouse esophageal biology
title_short Generation and characterization of an inducible transgenic model for studying mouse esophageal biology
title_full Generation and characterization of an inducible transgenic model for studying mouse esophageal biology
title_fullStr Generation and characterization of an inducible transgenic model for studying mouse esophageal biology
title_full_unstemmed Generation and characterization of an inducible transgenic model for studying mouse esophageal biology
title_sort generation and characterization of an inducible transgenic model for studying mouse esophageal biology
publisher BMC
series BMC Developmental Biology
issn 1471-213X
publishDate 2012-06-01
description <p>Abstract</p> <p>Background</p> <p>To facilitate the <it>in vivo</it> study of esophageal (stem) cell biology in homeostasis and cancer, novel mouse models are necessary to elicit expression of candidate genes in a tissue-specific and inducible fashion. To this aim, we developed and studied a mouse model to allow labeling of esophageal cells with the histone 2B-GFP (H2B-GFP) fusion protein.</p> <p>Results</p> <p>First, we generated a transgenic mouse model expressing the reverse tetracycline transactivator rtTA2-M2 under control of the promoter (ED-L2) of the Epstein-Barr virus (EBV) gene encoding the latent membrane protein-1 (<it>LMP-1</it>). The newly generated ED-L2-rtTA2-M2 (ED-L2-rtTA) mice were then bred with the previously developed tetO-HIST1H2BJ/GFP (tetO-H2B-GFP) model to assess inducibility and tissue-specificity. Expression of the H2B-GFP fusion protein was observed upon doxycycline induction but was restricted to the terminally differentiated cells above the basal cell layer. To achieve expression in the basal compartment of the esophagus, we subsequently employed a different transgenic model expressing the reverse transactivator rtTA2S-M2 under the control of the ubiquitous, methylation-free CpG island of the human hnRNPA2B1-CBX3 gene (hnRNP-rtTA). Upon doxycycline administration to the compound hnRNP-rtTA/tetO-H2B-GFP mice, near-complete labeling of all esophageal cells was achieved. Pulse-chase experiments confirmed that complete turnover of the esophageal epithelium in the adult mouse is achieved within 7–10 days.</p> <p>Conclusions</p> <p>We show that the esophagus-specific promoter ED-L2 is expressed only in the differentiated cells above the basal layer. Moreover, we confirmed that esophageal turn-over in the adult mouse does not exceed 7–10 days.</p>
topic Mouse
Esophagus
Turnover rate
Promoter
ED-L2
Doxycycline inducible
url http://www.biomedcentral.com/1471-213X/12/18
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AT monkhorstkim generationandcharacterizationofaninducibletransgenicmodelforstudyingmouseesophagealbiology
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