dc.contributor.author
Semaan, Marwan
dc.contributor.author
Ivanusic, Daniel
dc.contributor.author
Denner, Joachim
dc.date.accessioned
2018-06-08T03:24:05Z
dc.date.available
2015-06-11T11:48:01.611Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/15095
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-19283
dc.description.abstract
Xenotransplantation has been proposed as a solution to the shortage of
suitable human donors for transplantation and pigs are currently favoured as
donor animals. However, xenotransplantation may be associated with the
transmission of zoonotic microorganisms. Whereas most porcine microorganisms
representing a risk for the human recipient may be eliminated by designated
pathogen free breeding, multiple copies of porcine endogenous retroviruses
(PERVs) are integrated in the genome of all pigs and cannot be eliminated this
way. PERVs are released as infectious particles and infect human cells. The
zinc finger nuclease (ZFN) technology allows knocking out specifically
cellular genes, however it was not yet used to eliminate multiple integrated
proviral sequences with a strong conservation in the target sequence. To
reduce the risk of horizontal PERV transmission and to knock out as many as
possible proviruses, for the first time the powerful tool of the ZFN
technology was used. ZFN were designed to bind specifically to sequences
conserved in all known replication-competent proviruses. Expression and
transport of the ZFN into the nucleus was shown by Western blot analysis, co-
localisation analysis, PLA and FRET. Survival of transfected cells was
analysed using fluorescent ZFN and cell counting. After transfection a strong
expression of the ZFN proteins and a co-localisation of the expressed ZFN
proteins were shown. However, expression of the ZFN was found to be extremely
toxic for the transfected cells. The induced cytotoxicity was likely due to
the specific cutting of the high copy number of the PERV proviruses, which is
also commonly observed when ZFN with low specificity cleave numerous off-
target sites in a genome. This is the first attempt to knock out multiple,
nearly identical, genes in a cellular genome using ZFN. The attempt failed,
and other strategies should be used to prevent PERV transmission.
en
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::630 Landwirtschaft
dc.title
Cytotoxic Effects during Knock Out of Multiple Porcine Endogenous Retrovirus
(PERV) Sequences in the Pig Genome by Zinc Finger Nucleases (ZFN)
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
PLoS ONE. - 10 (2015), 4, Artikel Nr. e0122059
dcterms.bibliographicCitation.doi
10.1371/journal.pone.0122059
dcterms.bibliographicCitation.url
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0122059
refubium.affiliation
Biologie, Chemie, Pharmazie
de
refubium.mycore.fudocsId
FUDOCS_document_000000022618
refubium.note.author
Der Artikel wurde in einer Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000005036
dcterms.accessRights.openaire
open access