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@ARTICLE{Imahorn:885963,
author = {Imahorn, Elias and Aushev, Magomet and Herms, Stefan and
Hoffmann, Per and Cichon, Sven and Reichelt, Julia and Itin,
Peter H. and Burger, Bettina},
title = {{G}ene expression is stable in a complete {CIB}1 knockout
keratinocyte model},
journal = {Scientific reports},
volume = {10},
number = {1},
issn = {2045-2322},
address = {[London]},
publisher = {Macmillan Publishers Limited, part of Springer Nature},
reportid = {FZJ-2020-04194},
pages = {14952},
year = {2020},
abstract = {Epidermodysplasia verruciformis (EV) is a genodermatosis
characterized by the inability of keratinocytes to control
cutaneous β-HPV infection and a high risk for non-melanoma
skin cancer (NMSC). Bi-allelic loss of function variants in
TMC6, TMC8, and CIB1 predispose to EV. The correlation
between these proteins and β-HPV infection is unclear. Its
elucidation will advance the understanding of HPV control in
human keratinocytes and development of NMSC. We generated a
cell culture model by CRISPR/Cas9-mediated deletion of CIB1
to study the function of CIB1 in keratinocytes. Nine CIB1
knockout and nine mock control clones were generated
originating from a human keratinocyte line. We observed
small changes in gene expression as a result of CIB1
knockout, which is consistent with the clearly defined
phenotype of EV patients. This suggests that the function of
human CIB1 in keratinocytes is limited and involves the
restriction of β-HPV. The presented model is useful to
investigate CIB1 interaction with β-HPV in future studies.},
cin = {INM-1},
ddc = {600},
cid = {I:(DE-Juel1)INM-1-20090406},
pnm = {571 - Connectivity and Activity (POF3-571)},
pid = {G:(DE-HGF)POF3-571},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:32917957},
UT = {WOS:000572424900007},
doi = {10.1038/s41598-020-71889-9},
url = {https://juser.fz-juelich.de/record/885963},
}