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@ARTICLE{Toda:268496,
author = {Toda, Tomohisa and Bedrosian, Tracy A and Schafer, Simon T
and Cuoco, Michael S and Linker, Sara B and Ghassemzadeh,
Saeed and Mitchell, Lisa and Whiteley, Jack T and Novaresi,
Nicole and McDonald, Aidan H and Gallina, Iryna S and Yoon,
Hyojung and Hester, Mark E and Pena, Monique and Lim,
Christina and Suljic, Emelia and AlFatah Mansour, Abed and
Boulard, Matthieu and Parylak, Sarah L and Gage, Fred H},
title = {{L}ong interspersed nuclear elements safeguard neural
progenitors from precocious differentiation.},
journal = {Cell reports},
volume = {43},
number = {2},
issn = {2211-1247},
address = {[New York, NY]},
publisher = {Elsevier},
reportid = {DZNE-2024-00242},
pages = {113774},
year = {2024},
abstract = {Long interspersed nuclear element-1 (L1 or LINE-1) is a
highly abundant mobile genetic element in both humans and
mice, comprising almost $20\%$ of each genome. L1s are
silenced by several mechanisms, as their uncontrolled
expression has the potential to induce genomic instability.
However, L1s are paradoxically expressed at high levels in
differentiating neural progenitor cells. Using in vitro and
in vivo techniques to modulate L1 expression, we report that
L1s play a critical role in both human and mouse brain
development by regulating the rate of neural differentiation
in a reverse-transcription-independent manner.},
keywords = {Humans / Animals / Mice / Cell Differentiation / Genomic
Instability / Long Interspersed Nucleotide Elements / Neural
Stem Cells / CP: Developmental biology (Other) / CP:
Neuroscience (Other) / L1 (Other) / LINE-1 (Other) / brain
development (Other) / neural progenitor cells (Other) /
repetitive elements (Other)},
cin = {AG Toda},
ddc = {610},
cid = {I:(DE-2719)1710014},
pnm = {352 - Disease Mechanisms (POF4-352)},
pid = {G:(DE-HGF)POF4-352},
typ = {PUB:(DE-HGF)16},
pmc = {pmc:PMC10948021},
pubmed = {pmid:38349791},
doi = {10.1016/j.celrep.2024.113774},
url = {https://pub.dzne.de/record/268496},
}