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Development of Retroviral Vectors for Tissue-Restricted Expression in Chicken Embryonic Gonads
The chicken embryo has long been a useful model organism for studying development, including sex determination and gonadal differentiation. However, manipulating gene expression specifically in the embryonic avian gonad has been difficult. The viral vector RCASBP can be readily used for embryo-wide...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086957/ https://www.ncbi.nlm.nih.gov/pubmed/25003592 http://dx.doi.org/10.1371/journal.pone.0101811 |
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author | Lambeth, Luke S. Ohnesorg, Thomas Cummins, David M. Sinclair, Andrew H. Smith, Craig A. |
author_facet | Lambeth, Luke S. Ohnesorg, Thomas Cummins, David M. Sinclair, Andrew H. Smith, Craig A. |
author_sort | Lambeth, Luke S. |
collection | PubMed |
description | The chicken embryo has long been a useful model organism for studying development, including sex determination and gonadal differentiation. However, manipulating gene expression specifically in the embryonic avian gonad has been difficult. The viral vector RCASBP can be readily used for embryo-wide transgene expression; however global mis-expression using this method can cause deleterious off-target effects and embryo-lethality. In an attempt to develop vectors for the over-expression of sequences in chicken embryonic urogenital tissues, the viral vector RCANBP was engineered to contain predicted promoter sequences of gonadal-expressed genes. Several promoters were analysed and it was found that although the SF1 promoter produced a tissue-restricted expression pattern that was highest in the mesonephros and liver, it was also higher in the gonads compared to the rest of the body. The location of EGFP expression from the SF1 promoter overlapped with several key gonad-expressed sex development genes; however expression was generally low-level and was not seen in all gonadal cells. To further validate this sequence the key testis determinant DMRT1 was over-expressed in female embryos, which due to insufficient levels had no effect on gonad development. The female gene aromatase was then over-expressed in male embryos, which disrupted the testis pathway as demonstrated by a reduction in AMH protein. Taken together, although these data showed that the SF1 promoter can be used for functional studies in ovo, a stronger promoter sequence would likely be required for the functional analysis of gonad genes that require high-level expression. |
format | Online Article Text |
id | pubmed-4086957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40869572014-07-14 Development of Retroviral Vectors for Tissue-Restricted Expression in Chicken Embryonic Gonads Lambeth, Luke S. Ohnesorg, Thomas Cummins, David M. Sinclair, Andrew H. Smith, Craig A. PLoS One Research Article The chicken embryo has long been a useful model organism for studying development, including sex determination and gonadal differentiation. However, manipulating gene expression specifically in the embryonic avian gonad has been difficult. The viral vector RCASBP can be readily used for embryo-wide transgene expression; however global mis-expression using this method can cause deleterious off-target effects and embryo-lethality. In an attempt to develop vectors for the over-expression of sequences in chicken embryonic urogenital tissues, the viral vector RCANBP was engineered to contain predicted promoter sequences of gonadal-expressed genes. Several promoters were analysed and it was found that although the SF1 promoter produced a tissue-restricted expression pattern that was highest in the mesonephros and liver, it was also higher in the gonads compared to the rest of the body. The location of EGFP expression from the SF1 promoter overlapped with several key gonad-expressed sex development genes; however expression was generally low-level and was not seen in all gonadal cells. To further validate this sequence the key testis determinant DMRT1 was over-expressed in female embryos, which due to insufficient levels had no effect on gonad development. The female gene aromatase was then over-expressed in male embryos, which disrupted the testis pathway as demonstrated by a reduction in AMH protein. Taken together, although these data showed that the SF1 promoter can be used for functional studies in ovo, a stronger promoter sequence would likely be required for the functional analysis of gonad genes that require high-level expression. Public Library of Science 2014-07-08 /pmc/articles/PMC4086957/ /pubmed/25003592 http://dx.doi.org/10.1371/journal.pone.0101811 Text en © 2014 Lambeth 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 Lambeth, Luke S. Ohnesorg, Thomas Cummins, David M. Sinclair, Andrew H. Smith, Craig A. Development of Retroviral Vectors for Tissue-Restricted Expression in Chicken Embryonic Gonads |
title | Development of Retroviral Vectors for Tissue-Restricted Expression in Chicken Embryonic Gonads |
title_full | Development of Retroviral Vectors for Tissue-Restricted Expression in Chicken Embryonic Gonads |
title_fullStr | Development of Retroviral Vectors for Tissue-Restricted Expression in Chicken Embryonic Gonads |
title_full_unstemmed | Development of Retroviral Vectors for Tissue-Restricted Expression in Chicken Embryonic Gonads |
title_short | Development of Retroviral Vectors for Tissue-Restricted Expression in Chicken Embryonic Gonads |
title_sort | development of retroviral vectors for tissue-restricted expression in chicken embryonic gonads |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086957/ https://www.ncbi.nlm.nih.gov/pubmed/25003592 http://dx.doi.org/10.1371/journal.pone.0101811 |
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