The Potential Regulation of L1 Mobility by RNA Interference
The hypothesis that RNA interference constrains L1 mobility seems inherently reasonable: L1 mobility can be dangerous and L1 RNA, the presumed target of RNAi, serves as a critical retrotransposition intermediate. Despite its plausibility, proof for this hypothesis has been difficult to obtain. Studi...
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Online Access: | http://dx.doi.org/10.1155/JBB/2006/32713 |
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doaj-bb65a0509412451584bbbbaef98735322020-11-25T01:37:59ZengHindawi LimitedJournal of Biomedicine and Biotechnology1110-72431110-72512006-01-01200610.1155/JBB/2006/3271332713The Potential Regulation of L1 Mobility by RNA InterferenceShane R. Horman0Petr Svoboda1Eline T. Luning Prak2Department of Pathology and Laboratory Medicine, School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6055, USAFriedrich Miescher Institute for Biomedical Research, Maulbeerstrasse 66, Basel 4058, SwitzerlandDepartment of Pathology and Laboratory Medicine, School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6055, USAThe hypothesis that RNA interference constrains L1 mobility seems inherently reasonable: L1 mobility can be dangerous and L1 RNA, the presumed target of RNAi, serves as a critical retrotransposition intermediate. Despite its plausibility, proof for this hypothesis has been difficult to obtain. Studies attempting to link the L1 retrotransposition frequency to alterations in RNAi activity have been hampered by the long times required to measure retrotransposition frequency, the pleiotropic and toxic effects of altering RNAi over similar time periods, and the possibility that other cellular machinery may contribute to the regulation of L1s. Another problem is that the commonly used L1 reporter cassette may serve as a substrate for RNAi. Here we review the L1-RNAi hypothesis and describe a genetic assay with a modified reporter cassette that detects approximately 4 times more L1 insertions than the conventional retrotransposition assay.http://dx.doi.org/10.1155/JBB/2006/32713 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shane R. Horman Petr Svoboda Eline T. Luning Prak |
spellingShingle |
Shane R. Horman Petr Svoboda Eline T. Luning Prak The Potential Regulation of L1 Mobility by RNA Interference Journal of Biomedicine and Biotechnology |
author_facet |
Shane R. Horman Petr Svoboda Eline T. Luning Prak |
author_sort |
Shane R. Horman |
title |
The Potential Regulation of L1 Mobility by RNA Interference |
title_short |
The Potential Regulation of L1 Mobility by RNA Interference |
title_full |
The Potential Regulation of L1 Mobility by RNA Interference |
title_fullStr |
The Potential Regulation of L1 Mobility by RNA Interference |
title_full_unstemmed |
The Potential Regulation of L1 Mobility by RNA Interference |
title_sort |
potential regulation of l1 mobility by rna interference |
publisher |
Hindawi Limited |
series |
Journal of Biomedicine and Biotechnology |
issn |
1110-7243 1110-7251 |
publishDate |
2006-01-01 |
description |
The hypothesis that RNA interference constrains L1 mobility seems
inherently reasonable: L1 mobility can be dangerous and L1 RNA,
the presumed target of RNAi, serves as a critical
retrotransposition intermediate. Despite its plausibility, proof
for this hypothesis has been difficult to obtain. Studies
attempting to link the L1 retrotransposition frequency to
alterations in RNAi activity have been hampered by the long times
required to measure retrotransposition frequency, the pleiotropic
and toxic effects of altering RNAi over similar time periods, and
the possibility that other cellular machinery may contribute to
the regulation of L1s. Another problem is that the commonly used
L1 reporter cassette may serve as a substrate for RNAi. Here we
review the L1-RNAi hypothesis and describe a genetic assay with a
modified reporter cassette that detects approximately 4 times more
L1 insertions than the conventional retrotransposition assay. |
url |
http://dx.doi.org/10.1155/JBB/2006/32713 |
work_keys_str_mv |
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