Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
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
_version_ 1782152510877728768
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
work_keys_str_mv AT meehandanielt genetargetinginadultrhesusmacaquefibroblasts
AT zinkmaryann genetargetinginadultrhesusmacaquefibroblasts
AT mahlenmelissa genetargetinginadultrhesusmacaquefibroblasts
AT nelsonmarilu genetargetinginadultrhesusmacaquefibroblasts
AT sangerwarreng genetargetinginadultrhesusmacaquefibroblasts
AT mitalipovshoukhratm genetargetinginadultrhesusmacaquefibroblasts
AT wolfdonp genetargetinginadultrhesusmacaquefibroblasts
AT ouellettemichelm genetargetinginadultrhesusmacaquefibroblasts
AT norgrenrobertb genetargetinginadultrhesusmacaquefibroblasts