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Production of transgenic strawberries by temporary immersion bioreactor system and verification by TAIL-PCR

BACKGROUND: Strawberry (Fragaria × ananassa) is an economically important soft fruit crop with polyploid genome which complicates the breeding of new cultivars. For certain traits, genetic engineering offers a potential alternative to traditional breeding. However, many strawberry varieties are quit...

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Autores principales: Hanhineva, Kati J, Kärenlampi, Sirpa O
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1810528/
https://www.ncbi.nlm.nih.gov/pubmed/17309794
http://dx.doi.org/10.1186/1472-6750-7-11
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author Hanhineva, Kati J
Kärenlampi, Sirpa O
author_facet Hanhineva, Kati J
Kärenlampi, Sirpa O
author_sort Hanhineva, Kati J
collection PubMed
description BACKGROUND: Strawberry (Fragaria × ananassa) is an economically important soft fruit crop with polyploid genome which complicates the breeding of new cultivars. For certain traits, genetic engineering offers a potential alternative to traditional breeding. However, many strawberry varieties are quite recalcitrant for Agrobacterium-mediated transformation, and a method allowing easy handling of large amounts of starting material is needed. Also the genotyping of putative transformants is challenging since the isolation of DNA for Southern analysis is difficult due to the high amount of phenolic compounds and polysaccharides that complicate efficient extraction of digestable DNA. There is thus a need to apply a screening method that is sensitive and unambiguous in identifying the different transformation events. RESULTS: Hygromycin-resistant strawberries were developed in temporary immersion bioreactors by Agrobacterium-mediated gene transfer. Putative transformants were screened by TAIL-PCR to verify T-DNA integration and to distinguish between the individual transformation events. Several different types of border sequence arrangements were detected. CONCLUSION: This study demonstrates that temporary immersion bioreactor system suits well for the regeneration of transgenic strawberry plants as a labour-efficient technique. Small amount of DNA required by TAIL-PCR is easily recovered even from a small transformant, which allows rapid verification of T-DNA integration and detection of separate gene transfer events. These techniques combined clearly facilitate the generation of transgenic strawberries but should be applicable to other plants as well.
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spelling pubmed-18105282007-03-07 Production of transgenic strawberries by temporary immersion bioreactor system and verification by TAIL-PCR Hanhineva, Kati J Kärenlampi, Sirpa O BMC Biotechnol Methodology Article BACKGROUND: Strawberry (Fragaria × ananassa) is an economically important soft fruit crop with polyploid genome which complicates the breeding of new cultivars. For certain traits, genetic engineering offers a potential alternative to traditional breeding. However, many strawberry varieties are quite recalcitrant for Agrobacterium-mediated transformation, and a method allowing easy handling of large amounts of starting material is needed. Also the genotyping of putative transformants is challenging since the isolation of DNA for Southern analysis is difficult due to the high amount of phenolic compounds and polysaccharides that complicate efficient extraction of digestable DNA. There is thus a need to apply a screening method that is sensitive and unambiguous in identifying the different transformation events. RESULTS: Hygromycin-resistant strawberries were developed in temporary immersion bioreactors by Agrobacterium-mediated gene transfer. Putative transformants were screened by TAIL-PCR to verify T-DNA integration and to distinguish between the individual transformation events. Several different types of border sequence arrangements were detected. CONCLUSION: This study demonstrates that temporary immersion bioreactor system suits well for the regeneration of transgenic strawberry plants as a labour-efficient technique. Small amount of DNA required by TAIL-PCR is easily recovered even from a small transformant, which allows rapid verification of T-DNA integration and detection of separate gene transfer events. These techniques combined clearly facilitate the generation of transgenic strawberries but should be applicable to other plants as well. BioMed Central 2007-02-19 /pmc/articles/PMC1810528/ /pubmed/17309794 http://dx.doi.org/10.1186/1472-6750-7-11 Text en Copyright © 2007 Hanhineva and Kärenlampi; 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
Hanhineva, Kati J
Kärenlampi, Sirpa O
Production of transgenic strawberries by temporary immersion bioreactor system and verification by TAIL-PCR
title Production of transgenic strawberries by temporary immersion bioreactor system and verification by TAIL-PCR
title_full Production of transgenic strawberries by temporary immersion bioreactor system and verification by TAIL-PCR
title_fullStr Production of transgenic strawberries by temporary immersion bioreactor system and verification by TAIL-PCR
title_full_unstemmed Production of transgenic strawberries by temporary immersion bioreactor system and verification by TAIL-PCR
title_short Production of transgenic strawberries by temporary immersion bioreactor system and verification by TAIL-PCR
title_sort production of transgenic strawberries by temporary immersion bioreactor system and verification by tail-pcr
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1810528/
https://www.ncbi.nlm.nih.gov/pubmed/17309794
http://dx.doi.org/10.1186/1472-6750-7-11
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