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Arginine methylation analysis of the splicing-associated SR protein SFRS9/SRP30C

The human SFRS9/SRp30c belongs to the SR family of splicing regulators. Despite evidence that members of this protein family may be targeted by arginine methylation, this has yet to be experimentally addressed. In this study, we found that SFRS9 is a target for PRMT1-mediated arginine methylation in...

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Autores principales: Bressan, Gustavo C., Moraes, Eduardo C., Manfiolli, Adriana O., Kuniyoshi, Tais M., Passos, Dario O., Gomes, Marcelo D., Kobarg, Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SP Versita 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275941/
https://www.ncbi.nlm.nih.gov/pubmed/19557313
http://dx.doi.org/10.2478/s11658-009-0024-2
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author Bressan, Gustavo C.
Moraes, Eduardo C.
Manfiolli, Adriana O.
Kuniyoshi, Tais M.
Passos, Dario O.
Gomes, Marcelo D.
Kobarg, Jörg
author_facet Bressan, Gustavo C.
Moraes, Eduardo C.
Manfiolli, Adriana O.
Kuniyoshi, Tais M.
Passos, Dario O.
Gomes, Marcelo D.
Kobarg, Jörg
author_sort Bressan, Gustavo C.
collection PubMed
description The human SFRS9/SRp30c belongs to the SR family of splicing regulators. Despite evidence that members of this protein family may be targeted by arginine methylation, this has yet to be experimentally addressed. In this study, we found that SFRS9 is a target for PRMT1-mediated arginine methylation in vitro, and that it is immunoprecipitated from HEK-293 lysates by antibodies that recognize both mono- and dimethylated arginines. We further observed that upon treatment with the methylation inhibitor Adox, the fluorescent EGFP-SFRS9 re-localizes to dot-like structures in the cell nucleus. In subsequent confocal analyses, we found that EGFP-SFRS9 localizes to nucleoli in Adox-treated cells. Our findings indicate the importance of arginine methylation for the subnuclear localization of SFRS9.
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spelling pubmed-62759412018-12-10 Arginine methylation analysis of the splicing-associated SR protein SFRS9/SRP30C Bressan, Gustavo C. Moraes, Eduardo C. Manfiolli, Adriana O. Kuniyoshi, Tais M. Passos, Dario O. Gomes, Marcelo D. Kobarg, Jörg Cell Mol Biol Lett Research Article The human SFRS9/SRp30c belongs to the SR family of splicing regulators. Despite evidence that members of this protein family may be targeted by arginine methylation, this has yet to be experimentally addressed. In this study, we found that SFRS9 is a target for PRMT1-mediated arginine methylation in vitro, and that it is immunoprecipitated from HEK-293 lysates by antibodies that recognize both mono- and dimethylated arginines. We further observed that upon treatment with the methylation inhibitor Adox, the fluorescent EGFP-SFRS9 re-localizes to dot-like structures in the cell nucleus. In subsequent confocal analyses, we found that EGFP-SFRS9 localizes to nucleoli in Adox-treated cells. Our findings indicate the importance of arginine methylation for the subnuclear localization of SFRS9. SP Versita 2009-06-25 /pmc/articles/PMC6275941/ /pubmed/19557313 http://dx.doi.org/10.2478/s11658-009-0024-2 Text en © © Versita Warsaw and Springer-Verlag Berlin Heidelberg 2009
spellingShingle Research Article
Bressan, Gustavo C.
Moraes, Eduardo C.
Manfiolli, Adriana O.
Kuniyoshi, Tais M.
Passos, Dario O.
Gomes, Marcelo D.
Kobarg, Jörg
Arginine methylation analysis of the splicing-associated SR protein SFRS9/SRP30C
title Arginine methylation analysis of the splicing-associated SR protein SFRS9/SRP30C
title_full Arginine methylation analysis of the splicing-associated SR protein SFRS9/SRP30C
title_fullStr Arginine methylation analysis of the splicing-associated SR protein SFRS9/SRP30C
title_full_unstemmed Arginine methylation analysis of the splicing-associated SR protein SFRS9/SRP30C
title_short Arginine methylation analysis of the splicing-associated SR protein SFRS9/SRP30C
title_sort arginine methylation analysis of the splicing-associated sr protein sfrs9/srp30c
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275941/
https://www.ncbi.nlm.nih.gov/pubmed/19557313
http://dx.doi.org/10.2478/s11658-009-0024-2
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