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Arginine methylation of Piwi proteins, catalyzed by dPRMT5, is required for Ago3 and Aub stability
Piwi family proteins are essential for germline development and bind piwi-interacting RNAs (piRNAs 1 2 3). The grandchildless gene aub of Drosophila melanogaster encodes the piRNA-binding protein Aub that is essential for formation of primordial germ cells (PGCs) 4. Here we report that mouse, Xenopu...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2746449/ https://www.ncbi.nlm.nih.gov/pubmed/19377467 http://dx.doi.org/10.1038/ncb1872 |
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author | Kirino, Yohei Kim, Namwoo de Planell-Saguer, Mariàngels Khandros, Eugene Chiorean, Stephanie Klein, Peter S. Rigoutsos, Isidore Jongens, Thomas A. Mourelatos, Zissimos |
author_facet | Kirino, Yohei Kim, Namwoo de Planell-Saguer, Mariàngels Khandros, Eugene Chiorean, Stephanie Klein, Peter S. Rigoutsos, Isidore Jongens, Thomas A. Mourelatos, Zissimos |
author_sort | Kirino, Yohei |
collection | PubMed |
description | Piwi family proteins are essential for germline development and bind piwi-interacting RNAs (piRNAs 1 2 3). The grandchildless gene aub of Drosophila melanogaster encodes the piRNA-binding protein Aub that is essential for formation of primordial germ cells (PGCs) 4. Here we report that mouse, Xenopus laevis and Drosophila melanogaster Piwi family proteins contain symmetrical dimethylarginines (sDMAs). We find that Piwi proteins are expressed in X. laevis oocytes and we identify numerous X. laevis piRNAs. We report that the Drosophila homolog of protein methyltransferase 5 (dPRMT5, csul/dart5), which is also the product of a grandchildless gene 5, 6, is required for arginine methylation of Drosophila Piwi, Ago3 and Aub proteins, in vivo. Loss of dPRMT5 activity leads to reduction of piRNAs and in particular of Ago3 and Aub protein levels and accumulation of retrotransposons in the Drosophila ovary. Our studies explain the relationship between aub and dPRMT5 (csul/dart5) genes by demonstrating that dPRMT5 is the enzyme that methylates Aub. Our findings underscore the significance of sDMA modification of Piwi proteins in the germline and suggest an interacting pathway of genes that are required for piRNA function and PGC specification. |
format | Text |
id | pubmed-2746449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
record_format | MEDLINE/PubMed |
spelling | pubmed-27464492009-11-01 Arginine methylation of Piwi proteins, catalyzed by dPRMT5, is required for Ago3 and Aub stability Kirino, Yohei Kim, Namwoo de Planell-Saguer, Mariàngels Khandros, Eugene Chiorean, Stephanie Klein, Peter S. Rigoutsos, Isidore Jongens, Thomas A. Mourelatos, Zissimos Nat Cell Biol Article Piwi family proteins are essential for germline development and bind piwi-interacting RNAs (piRNAs 1 2 3). The grandchildless gene aub of Drosophila melanogaster encodes the piRNA-binding protein Aub that is essential for formation of primordial germ cells (PGCs) 4. Here we report that mouse, Xenopus laevis and Drosophila melanogaster Piwi family proteins contain symmetrical dimethylarginines (sDMAs). We find that Piwi proteins are expressed in X. laevis oocytes and we identify numerous X. laevis piRNAs. We report that the Drosophila homolog of protein methyltransferase 5 (dPRMT5, csul/dart5), which is also the product of a grandchildless gene 5, 6, is required for arginine methylation of Drosophila Piwi, Ago3 and Aub proteins, in vivo. Loss of dPRMT5 activity leads to reduction of piRNAs and in particular of Ago3 and Aub protein levels and accumulation of retrotransposons in the Drosophila ovary. Our studies explain the relationship between aub and dPRMT5 (csul/dart5) genes by demonstrating that dPRMT5 is the enzyme that methylates Aub. Our findings underscore the significance of sDMA modification of Piwi proteins in the germline and suggest an interacting pathway of genes that are required for piRNA function and PGC specification. 2009-04-19 2009-05 /pmc/articles/PMC2746449/ /pubmed/19377467 http://dx.doi.org/10.1038/ncb1872 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Kirino, Yohei Kim, Namwoo de Planell-Saguer, Mariàngels Khandros, Eugene Chiorean, Stephanie Klein, Peter S. Rigoutsos, Isidore Jongens, Thomas A. Mourelatos, Zissimos Arginine methylation of Piwi proteins, catalyzed by dPRMT5, is required for Ago3 and Aub stability |
title | Arginine methylation of Piwi proteins, catalyzed by dPRMT5, is required for Ago3 and Aub stability |
title_full | Arginine methylation of Piwi proteins, catalyzed by dPRMT5, is required for Ago3 and Aub stability |
title_fullStr | Arginine methylation of Piwi proteins, catalyzed by dPRMT5, is required for Ago3 and Aub stability |
title_full_unstemmed | Arginine methylation of Piwi proteins, catalyzed by dPRMT5, is required for Ago3 and Aub stability |
title_short | Arginine methylation of Piwi proteins, catalyzed by dPRMT5, is required for Ago3 and Aub stability |
title_sort | arginine methylation of piwi proteins, catalyzed by dprmt5, is required for ago3 and aub stability |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2746449/ https://www.ncbi.nlm.nih.gov/pubmed/19377467 http://dx.doi.org/10.1038/ncb1872 |
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