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Application of a Novel Strategy of Engineering Conditional Alleles to a Single Exon Gene, Sox2

BACKGROUND: The Conditional by Inversion (COIN) method for engineering conditional alleles relies on an invertible optimized gene trap-like element, the COIN module, for imparting conditionality. The COIN module contains an optimized 3′ splice site-polyadenylation signal pair, but is inserted antise...

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Autores principales: Mandalos, Nikolaos, Saridaki, Marannia, Harper, Jessica Lea, Kotsoni, Anastasia, Yang, Peter, Economides, Aris N., Remboutsika, Eumorphia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3459942/
https://www.ncbi.nlm.nih.gov/pubmed/23029233
http://dx.doi.org/10.1371/journal.pone.0045768
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author Mandalos, Nikolaos
Saridaki, Marannia
Harper, Jessica Lea
Kotsoni, Anastasia
Yang, Peter
Economides, Aris N.
Remboutsika, Eumorphia
author_facet Mandalos, Nikolaos
Saridaki, Marannia
Harper, Jessica Lea
Kotsoni, Anastasia
Yang, Peter
Economides, Aris N.
Remboutsika, Eumorphia
author_sort Mandalos, Nikolaos
collection PubMed
description BACKGROUND: The Conditional by Inversion (COIN) method for engineering conditional alleles relies on an invertible optimized gene trap-like element, the COIN module, for imparting conditionality. The COIN module contains an optimized 3′ splice site-polyadenylation signal pair, but is inserted antisense to the target gene and therefore does not alter transcription, until it is inverted by Cre recombinase. In order to make COIN applicable to all protein-coding genes, the COIN module has been engineered within an artificial intron, enabling insertion into an exon. METHODOLOGY/PRINCIPAL FINDINGS: Therefore, theoretically, the COIN method should be applicable to single exon genes, and to test this idea we engineered a COIN allele of Sox2. This single exon gene presents additional design challenges, in that its proximal promoter and coding region are entirely contained within a CpG island, and are also spanned by an overlapping transcript, Sox2Ot, which contains mmu-miR1897. Here, we show that despite disruption of the CpG island by the COIN module intron, the COIN allele of Sox2 (Sox2(COIN)) is phenotypically wild type, and also does not interfere with expression of Sox2Ot and miR1897. Furthermore, the inverted COIN allele of Sox2, Sox2(INV) is functionally null, as homozygotes recapitulate the phenotype of Sox2(ßgeo/ßgeo) mice, a well-characterized Sox2 null. Lastly, the benefit of the eGFP marker embedded in the COIN allele is demonstrated as it mirrors the expression pattern of Sox2. CONCLUSIONS/SIGNIFICANCE: Our results demonstrate the applicability of the COIN technology as a method of choice for targeting single exon genes.
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spelling pubmed-34599422012-10-01 Application of a Novel Strategy of Engineering Conditional Alleles to a Single Exon Gene, Sox2 Mandalos, Nikolaos Saridaki, Marannia Harper, Jessica Lea Kotsoni, Anastasia Yang, Peter Economides, Aris N. Remboutsika, Eumorphia PLoS One Research Article BACKGROUND: The Conditional by Inversion (COIN) method for engineering conditional alleles relies on an invertible optimized gene trap-like element, the COIN module, for imparting conditionality. The COIN module contains an optimized 3′ splice site-polyadenylation signal pair, but is inserted antisense to the target gene and therefore does not alter transcription, until it is inverted by Cre recombinase. In order to make COIN applicable to all protein-coding genes, the COIN module has been engineered within an artificial intron, enabling insertion into an exon. METHODOLOGY/PRINCIPAL FINDINGS: Therefore, theoretically, the COIN method should be applicable to single exon genes, and to test this idea we engineered a COIN allele of Sox2. This single exon gene presents additional design challenges, in that its proximal promoter and coding region are entirely contained within a CpG island, and are also spanned by an overlapping transcript, Sox2Ot, which contains mmu-miR1897. Here, we show that despite disruption of the CpG island by the COIN module intron, the COIN allele of Sox2 (Sox2(COIN)) is phenotypically wild type, and also does not interfere with expression of Sox2Ot and miR1897. Furthermore, the inverted COIN allele of Sox2, Sox2(INV) is functionally null, as homozygotes recapitulate the phenotype of Sox2(ßgeo/ßgeo) mice, a well-characterized Sox2 null. Lastly, the benefit of the eGFP marker embedded in the COIN allele is demonstrated as it mirrors the expression pattern of Sox2. CONCLUSIONS/SIGNIFICANCE: Our results demonstrate the applicability of the COIN technology as a method of choice for targeting single exon genes. Public Library of Science 2012-09-27 /pmc/articles/PMC3459942/ /pubmed/23029233 http://dx.doi.org/10.1371/journal.pone.0045768 Text en © 2012 Mandalos et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Mandalos, Nikolaos
Saridaki, Marannia
Harper, Jessica Lea
Kotsoni, Anastasia
Yang, Peter
Economides, Aris N.
Remboutsika, Eumorphia
Application of a Novel Strategy of Engineering Conditional Alleles to a Single Exon Gene, Sox2
title Application of a Novel Strategy of Engineering Conditional Alleles to a Single Exon Gene, Sox2
title_full Application of a Novel Strategy of Engineering Conditional Alleles to a Single Exon Gene, Sox2
title_fullStr Application of a Novel Strategy of Engineering Conditional Alleles to a Single Exon Gene, Sox2
title_full_unstemmed Application of a Novel Strategy of Engineering Conditional Alleles to a Single Exon Gene, Sox2
title_short Application of a Novel Strategy of Engineering Conditional Alleles to a Single Exon Gene, Sox2
title_sort application of a novel strategy of engineering conditional alleles to a single exon gene, sox2
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3459942/
https://www.ncbi.nlm.nih.gov/pubmed/23029233
http://dx.doi.org/10.1371/journal.pone.0045768
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