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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Main Authors: Shane R. Horman, Petr Svoboda, Eline T. Luning Prak
Format: Article
Language:English
Published: Hindawi Limited 2006-01-01
Series:Journal of Biomedicine and Biotechnology
Online Access:http://dx.doi.org/10.1155/JBB/2006/32713
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spelling 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
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