Quantification of DNA binding, uptake, transmission and expression in bovine sperm mediated gene transfer by RT-PCR: Effect of transfection reagent and DNA architecture

In this study, we compared the transfection effectiveness of liposomes with the new transfection reagent FuGene 6 in bovine sperm mediated gene transfer (SMGT). Furthermore, we examined whether plasmid architecture affects overall efficiency by comparing two plasmids, one of them bearing an addition...

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Main Authors: Michael Hoelker, Supamit Mekchay, Hendrik Schneider, Benjamin Gaylord Bracket, Dawit Tesfaye, Danyel Jennen, Ernst Tholen, Markus Gilles, Franka Rings, Josef Griese, Karl Schellander
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/60826
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-608262018-09-10T04:11:27Z Quantification of DNA binding, uptake, transmission and expression in bovine sperm mediated gene transfer by RT-PCR: Effect of transfection reagent and DNA architecture Michael Hoelker Supamit Mekchay Hendrik Schneider Benjamin Gaylord Bracket Dawit Tesfaye Danyel Jennen Ernst Tholen Markus Gilles Franka Rings Josef Griese Karl Schellander Agricultural and Biological Sciences Veterinary In this study, we compared the transfection effectiveness of liposomes with the new transfection reagent FuGene 6 in bovine sperm mediated gene transfer (SMGT). Furthermore, we examined whether plasmid architecture affects overall efficiency by comparing two plasmids, one of them bearing an additional murine nontranscribed spacer (nts) insert (CMV-INF-τ-IRES-EGFP versus CMV-INF-τ-IRES-EGFP-nts). To accomplish that, we quantified plasmid binding and uptake to spermatozoon and transfer and expression of foreign DNA into embryos by real time PCR. More plasmids bound to spermatozoa when treated with FuGene 6 than with liposome treatment (p < 0.05) reaching highest counts in plasmids bearing the nts sequence (p < 0.05). Mean number of plasmids taken up was significantly (p < 0.05) affected by transfection strategy (1-3 versus 15-81 versus 120-162) with plasmids bearing the nts sequence being 2-8 fold more effective (p < 0.05). Culture of SMGT derived embryos up to day 9 did not result in any difference in terms of cleavage rate (64.2-84.2%) and development to blastocyst stage (18.8-26.3%) between different groups. Insert of the nts fragment significantly (p < 0.05) affected mean number of transmitted plasmids to 4-cell stage embryos (44 versus 7) and relative INF-τ mRNA expression level in day 9 blastocysts (7-8 fold). However, only six blastocysts (3.6%) exhibited green fluorescence indicating low EGFP protein production. In conclusion, we were able to show effectiveness of sperm mediated gene transfer is significantly affected by choice of transfection reagent and by plasmid architecture. © 2007 Elsevier Inc. All rights reserved. 2018-09-10T04:00:06Z 2018-09-10T04:00:06Z 2007-04-01 Journal 0093691X 2-s2.0-33847607522 10.1016/j.theriogenology.2006.12.011 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33847607522&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/60826
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Agricultural and Biological Sciences
Veterinary
spellingShingle Agricultural and Biological Sciences
Veterinary
Michael Hoelker
Supamit Mekchay
Hendrik Schneider
Benjamin Gaylord Bracket
Dawit Tesfaye
Danyel Jennen
Ernst Tholen
Markus Gilles
Franka Rings
Josef Griese
Karl Schellander
Quantification of DNA binding, uptake, transmission and expression in bovine sperm mediated gene transfer by RT-PCR: Effect of transfection reagent and DNA architecture
description In this study, we compared the transfection effectiveness of liposomes with the new transfection reagent FuGene 6 in bovine sperm mediated gene transfer (SMGT). Furthermore, we examined whether plasmid architecture affects overall efficiency by comparing two plasmids, one of them bearing an additional murine nontranscribed spacer (nts) insert (CMV-INF-τ-IRES-EGFP versus CMV-INF-τ-IRES-EGFP-nts). To accomplish that, we quantified plasmid binding and uptake to spermatozoon and transfer and expression of foreign DNA into embryos by real time PCR. More plasmids bound to spermatozoa when treated with FuGene 6 than with liposome treatment (p < 0.05) reaching highest counts in plasmids bearing the nts sequence (p < 0.05). Mean number of plasmids taken up was significantly (p < 0.05) affected by transfection strategy (1-3 versus 15-81 versus 120-162) with plasmids bearing the nts sequence being 2-8 fold more effective (p < 0.05). Culture of SMGT derived embryos up to day 9 did not result in any difference in terms of cleavage rate (64.2-84.2%) and development to blastocyst stage (18.8-26.3%) between different groups. Insert of the nts fragment significantly (p < 0.05) affected mean number of transmitted plasmids to 4-cell stage embryos (44 versus 7) and relative INF-τ mRNA expression level in day 9 blastocysts (7-8 fold). However, only six blastocysts (3.6%) exhibited green fluorescence indicating low EGFP protein production. In conclusion, we were able to show effectiveness of sperm mediated gene transfer is significantly affected by choice of transfection reagent and by plasmid architecture. © 2007 Elsevier Inc. All rights reserved.
format Journal
author Michael Hoelker
Supamit Mekchay
Hendrik Schneider
Benjamin Gaylord Bracket
Dawit Tesfaye
Danyel Jennen
Ernst Tholen
Markus Gilles
Franka Rings
Josef Griese
Karl Schellander
author_facet Michael Hoelker
Supamit Mekchay
Hendrik Schneider
Benjamin Gaylord Bracket
Dawit Tesfaye
Danyel Jennen
Ernst Tholen
Markus Gilles
Franka Rings
Josef Griese
Karl Schellander
author_sort Michael Hoelker
title Quantification of DNA binding, uptake, transmission and expression in bovine sperm mediated gene transfer by RT-PCR: Effect of transfection reagent and DNA architecture
title_short Quantification of DNA binding, uptake, transmission and expression in bovine sperm mediated gene transfer by RT-PCR: Effect of transfection reagent and DNA architecture
title_full Quantification of DNA binding, uptake, transmission and expression in bovine sperm mediated gene transfer by RT-PCR: Effect of transfection reagent and DNA architecture
title_fullStr Quantification of DNA binding, uptake, transmission and expression in bovine sperm mediated gene transfer by RT-PCR: Effect of transfection reagent and DNA architecture
title_full_unstemmed Quantification of DNA binding, uptake, transmission and expression in bovine sperm mediated gene transfer by RT-PCR: Effect of transfection reagent and DNA architecture
title_sort quantification of dna binding, uptake, transmission and expression in bovine sperm mediated gene transfer by rt-pcr: effect of transfection reagent and dna architecture
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33847607522&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/60826
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