MOV10 RNA Helicase Is a Potent Inhibitor of Retrotransposition in Cells

MOV10 protein, a putative RNA helicase and component of the RNA–induced silencing complex (RISC), inhibits retrovirus replication. We show that MOV10 also severely restricts human LINE1 (L1), Alu, and SVA retrotransposons. MOV10 associates with the L1 ribonucleoprotein particle, along with other RNA...

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Main Authors: Goodier, John L., Cheung, Ling E., Kazazian, Haig H.
Format: Online
Language:English
Published: Public Library of Science 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475670/
id pubmed-3475670
recordtype oai_dc
spelling pubmed-34756702012-10-23 MOV10 RNA Helicase Is a Potent Inhibitor of Retrotransposition in Cells Goodier, John L. Cheung, Ling E. Kazazian, Haig H. Research Article MOV10 protein, a putative RNA helicase and component of the RNA–induced silencing complex (RISC), inhibits retrovirus replication. We show that MOV10 also severely restricts human LINE1 (L1), Alu, and SVA retrotransposons. MOV10 associates with the L1 ribonucleoprotein particle, along with other RNA helicases including DDX5, DHX9, DDX17, DDX21, and DDX39A. However, unlike MOV10, these other helicases do not strongly inhibit retrotransposition, an activity dependent upon intact helicase domains. MOV10 association with retrotransposons is further supported by its colocalization with L1 ORF1 protein in stress granules, by cytoplasmic structures associated with RNA silencing, and by the ability of MOV10 to reduce endogenous and ectopic L1 expression. The majority of the human genome is repetitive DNA, most of which is the detritus of millions of years of accumulated retrotransposition. Retrotransposons remain active mutagens, and their insertion can disrupt gene function. Therefore, the host has evolved defense mechanisms to protect against retrotransposition, an arsenal we are only beginning to understand. With homologs in other vertebrates, insects, and plants, MOV10 may represent an ancient and innate form of immunity against both infective viruses and endogenous retroelements. Public Library of Science 2012-10-18 /pmc/articles/PMC3475670/ /pubmed/23093941 http://dx.doi.org/10.1371/journal.pgen.1002941 Text en © 2012 Goodier et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Goodier, John L.
Cheung, Ling E.
Kazazian, Haig H.
spellingShingle Goodier, John L.
Cheung, Ling E.
Kazazian, Haig H.
MOV10 RNA Helicase Is a Potent Inhibitor of Retrotransposition in Cells
author_facet Goodier, John L.
Cheung, Ling E.
Kazazian, Haig H.
author_sort Goodier, John L.
title MOV10 RNA Helicase Is a Potent Inhibitor of Retrotransposition in Cells
title_short MOV10 RNA Helicase Is a Potent Inhibitor of Retrotransposition in Cells
title_full MOV10 RNA Helicase Is a Potent Inhibitor of Retrotransposition in Cells
title_fullStr MOV10 RNA Helicase Is a Potent Inhibitor of Retrotransposition in Cells
title_full_unstemmed MOV10 RNA Helicase Is a Potent Inhibitor of Retrotransposition in Cells
title_sort mov10 rna helicase is a potent inhibitor of retrotransposition in cells
description MOV10 protein, a putative RNA helicase and component of the RNA–induced silencing complex (RISC), inhibits retrovirus replication. We show that MOV10 also severely restricts human LINE1 (L1), Alu, and SVA retrotransposons. MOV10 associates with the L1 ribonucleoprotein particle, along with other RNA helicases including DDX5, DHX9, DDX17, DDX21, and DDX39A. However, unlike MOV10, these other helicases do not strongly inhibit retrotransposition, an activity dependent upon intact helicase domains. MOV10 association with retrotransposons is further supported by its colocalization with L1 ORF1 protein in stress granules, by cytoplasmic structures associated with RNA silencing, and by the ability of MOV10 to reduce endogenous and ectopic L1 expression. The majority of the human genome is repetitive DNA, most of which is the detritus of millions of years of accumulated retrotransposition. Retrotransposons remain active mutagens, and their insertion can disrupt gene function. Therefore, the host has evolved defense mechanisms to protect against retrotransposition, an arsenal we are only beginning to understand. With homologs in other vertebrates, insects, and plants, MOV10 may represent an ancient and innate form of immunity against both infective viruses and endogenous retroelements.
publisher Public Library of Science
publishDate 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475670/
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