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Gene targeting in adult rhesus macaque fibroblasts
BACKGROUND: Gene targeting in nonhuman primates has the potential to produce critical animal models for translational studies related to human diseases. Successful gene targeting in fibroblasts followed by somatic cell nuclear transfer (SCNT) has been achieved in several species of large mammals but...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2292692/ https://www.ncbi.nlm.nih.gov/pubmed/18366794 http://dx.doi.org/10.1186/1472-6750-8-31 |
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author | Meehan, Daniel T Zink, Mary Ann Mahlen, Melissa Nelson, Marilu Sanger, Warren G Mitalipov, Shoukhrat M Wolf, Don P Ouellette, Michel M Norgren, Robert B |
author_facet | Meehan, Daniel T Zink, Mary Ann Mahlen, Melissa Nelson, Marilu Sanger, Warren G Mitalipov, Shoukhrat M Wolf, Don P Ouellette, Michel M Norgren, Robert B |
author_sort | Meehan, Daniel T |
collection | PubMed |
description | BACKGROUND: Gene targeting in nonhuman primates has the potential to produce critical animal models for translational studies related to human diseases. Successful gene targeting in fibroblasts followed by somatic cell nuclear transfer (SCNT) has been achieved in several species of large mammals but not yet in primates. Our goal was to establish the protocols necessary to achieve gene targeting in primary culture of adult rhesus macaque fibroblasts as a first step in creating nonhuman primate models of genetic disease using nuclear transfer technology. RESULTS: A primary culture of adult male fibroblasts was transfected with hTERT to overcome senescence and allow long term in vitro manipulations. Successful gene targeting of the HPRT locus in rhesus macaques was achieved by electroporating S-phase synchronized cells with a construct containing a SV40 enhancer. CONCLUSION: The cell lines reported here could be used for the production of null mutant rhesus macaque models of human genetic disease using SCNT technology. In addition, given the close evolutionary relationship and biological similarity between rhesus macaques and humans, the protocols described here may prove useful in the genetic engineering of human somatic cells. |
format | Text |
id | pubmed-2292692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22926922008-04-12 Gene targeting in adult rhesus macaque fibroblasts Meehan, Daniel T Zink, Mary Ann Mahlen, Melissa Nelson, Marilu Sanger, Warren G Mitalipov, Shoukhrat M Wolf, Don P Ouellette, Michel M Norgren, Robert B BMC Biotechnol Methodology Article BACKGROUND: Gene targeting in nonhuman primates has the potential to produce critical animal models for translational studies related to human diseases. Successful gene targeting in fibroblasts followed by somatic cell nuclear transfer (SCNT) has been achieved in several species of large mammals but not yet in primates. Our goal was to establish the protocols necessary to achieve gene targeting in primary culture of adult rhesus macaque fibroblasts as a first step in creating nonhuman primate models of genetic disease using nuclear transfer technology. RESULTS: A primary culture of adult male fibroblasts was transfected with hTERT to overcome senescence and allow long term in vitro manipulations. Successful gene targeting of the HPRT locus in rhesus macaques was achieved by electroporating S-phase synchronized cells with a construct containing a SV40 enhancer. CONCLUSION: The cell lines reported here could be used for the production of null mutant rhesus macaque models of human genetic disease using SCNT technology. In addition, given the close evolutionary relationship and biological similarity between rhesus macaques and humans, the protocols described here may prove useful in the genetic engineering of human somatic cells. BioMed Central 2008-03-26 /pmc/articles/PMC2292692/ /pubmed/18366794 http://dx.doi.org/10.1186/1472-6750-8-31 Text en Copyright © 2008 Meehan et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Meehan, Daniel T Zink, Mary Ann Mahlen, Melissa Nelson, Marilu Sanger, Warren G Mitalipov, Shoukhrat M Wolf, Don P Ouellette, Michel M Norgren, Robert B Gene targeting in adult rhesus macaque fibroblasts |
title | Gene targeting in adult rhesus macaque fibroblasts |
title_full | Gene targeting in adult rhesus macaque fibroblasts |
title_fullStr | Gene targeting in adult rhesus macaque fibroblasts |
title_full_unstemmed | Gene targeting in adult rhesus macaque fibroblasts |
title_short | Gene targeting in adult rhesus macaque fibroblasts |
title_sort | gene targeting in adult rhesus macaque fibroblasts |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2292692/ https://www.ncbi.nlm.nih.gov/pubmed/18366794 http://dx.doi.org/10.1186/1472-6750-8-31 |
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