Cargando…

Genome-Wide Analysis of Transposon and Retroviral Insertions Reveals Preferential Integrations in Regions of DNA Flexibility

DNA transposons and retroviruses are important transgenic tools for genome engineering. An important consideration affecting the choice of transgenic vector is their insertion site preferences. Previous large-scale analyses of Ds transposon integration sites in plants were done on the basis of repor...

Descripción completa

Detalles Bibliográficos
Autores principales: Vrljicak, Pavle, Tao, Shijie, Varshney, Gaurav K., Quach, Helen Ngoc Bao, Joshi, Adita, LaFave, Matthew C., Burgess, Shawn M., Sampath, Karuna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4825651/
https://www.ncbi.nlm.nih.gov/pubmed/26818075
http://dx.doi.org/10.1534/g3.115.026849
_version_ 1782426250352001024
author Vrljicak, Pavle
Tao, Shijie
Varshney, Gaurav K.
Quach, Helen Ngoc Bao
Joshi, Adita
LaFave, Matthew C.
Burgess, Shawn M.
Sampath, Karuna
author_facet Vrljicak, Pavle
Tao, Shijie
Varshney, Gaurav K.
Quach, Helen Ngoc Bao
Joshi, Adita
LaFave, Matthew C.
Burgess, Shawn M.
Sampath, Karuna
author_sort Vrljicak, Pavle
collection PubMed
description DNA transposons and retroviruses are important transgenic tools for genome engineering. An important consideration affecting the choice of transgenic vector is their insertion site preferences. Previous large-scale analyses of Ds transposon integration sites in plants were done on the basis of reporter gene expression or germ-line transmission, making it difficult to discern vertebrate integration preferences. Here, we compare over 1300 Ds transposon integration sites in zebrafish with Tol2 transposon and retroviral integration sites. Genome-wide analysis shows that Ds integration sites in the presence or absence of marker selection are remarkably similar and distributed throughout the genome. No strict motif was found, but a preference for structural features in the target DNA associated with DNA flexibility (Twist, Tilt, Rise, Roll, Shift, and Slide) was observed. Remarkably, this feature is also found in transposon and retroviral integrations in maize and mouse cells. Our findings show that structural features influence the integration of heterologous DNA in genomes, and have implications for targeted genome engineering.
format Online
Article
Text
id pubmed-4825651
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Genetics Society of America
record_format MEDLINE/PubMed
spelling pubmed-48256512016-04-11 Genome-Wide Analysis of Transposon and Retroviral Insertions Reveals Preferential Integrations in Regions of DNA Flexibility Vrljicak, Pavle Tao, Shijie Varshney, Gaurav K. Quach, Helen Ngoc Bao Joshi, Adita LaFave, Matthew C. Burgess, Shawn M. Sampath, Karuna G3 (Bethesda) Investigations DNA transposons and retroviruses are important transgenic tools for genome engineering. An important consideration affecting the choice of transgenic vector is their insertion site preferences. Previous large-scale analyses of Ds transposon integration sites in plants were done on the basis of reporter gene expression or germ-line transmission, making it difficult to discern vertebrate integration preferences. Here, we compare over 1300 Ds transposon integration sites in zebrafish with Tol2 transposon and retroviral integration sites. Genome-wide analysis shows that Ds integration sites in the presence or absence of marker selection are remarkably similar and distributed throughout the genome. No strict motif was found, but a preference for structural features in the target DNA associated with DNA flexibility (Twist, Tilt, Rise, Roll, Shift, and Slide) was observed. Remarkably, this feature is also found in transposon and retroviral integrations in maize and mouse cells. Our findings show that structural features influence the integration of heterologous DNA in genomes, and have implications for targeted genome engineering. Genetics Society of America 2016-01-26 /pmc/articles/PMC4825651/ /pubmed/26818075 http://dx.doi.org/10.1534/g3.115.026849 Text en Copyright © 2016 Vrljicak et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Vrljicak, Pavle
Tao, Shijie
Varshney, Gaurav K.
Quach, Helen Ngoc Bao
Joshi, Adita
LaFave, Matthew C.
Burgess, Shawn M.
Sampath, Karuna
Genome-Wide Analysis of Transposon and Retroviral Insertions Reveals Preferential Integrations in Regions of DNA Flexibility
title Genome-Wide Analysis of Transposon and Retroviral Insertions Reveals Preferential Integrations in Regions of DNA Flexibility
title_full Genome-Wide Analysis of Transposon and Retroviral Insertions Reveals Preferential Integrations in Regions of DNA Flexibility
title_fullStr Genome-Wide Analysis of Transposon and Retroviral Insertions Reveals Preferential Integrations in Regions of DNA Flexibility
title_full_unstemmed Genome-Wide Analysis of Transposon and Retroviral Insertions Reveals Preferential Integrations in Regions of DNA Flexibility
title_short Genome-Wide Analysis of Transposon and Retroviral Insertions Reveals Preferential Integrations in Regions of DNA Flexibility
title_sort genome-wide analysis of transposon and retroviral insertions reveals preferential integrations in regions of dna flexibility
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4825651/
https://www.ncbi.nlm.nih.gov/pubmed/26818075
http://dx.doi.org/10.1534/g3.115.026849
work_keys_str_mv AT vrljicakpavle genomewideanalysisoftransposonandretroviralinsertionsrevealspreferentialintegrationsinregionsofdnaflexibility
AT taoshijie genomewideanalysisoftransposonandretroviralinsertionsrevealspreferentialintegrationsinregionsofdnaflexibility
AT varshneygauravk genomewideanalysisoftransposonandretroviralinsertionsrevealspreferentialintegrationsinregionsofdnaflexibility
AT quachhelenngocbao genomewideanalysisoftransposonandretroviralinsertionsrevealspreferentialintegrationsinregionsofdnaflexibility
AT joshiadita genomewideanalysisoftransposonandretroviralinsertionsrevealspreferentialintegrationsinregionsofdnaflexibility
AT lafavematthewc genomewideanalysisoftransposonandretroviralinsertionsrevealspreferentialintegrationsinregionsofdnaflexibility
AT burgessshawnm genomewideanalysisoftransposonandretroviralinsertionsrevealspreferentialintegrationsinregionsofdnaflexibility
AT sampathkaruna genomewideanalysisoftransposonandretroviralinsertionsrevealspreferentialintegrationsinregionsofdnaflexibility