Cargando…

SUMOylation Blocks the Ubiquitin-Mediated Degradation of the Nephronophthisis Gene Product Glis2/NPHP7

Glis2/NPHP7 is a transcriptional regulator mutated in type 7 nephronophthisis, an autosomal recessive ciliopathy associated with cystic and fibrotic kidney disease as well as characteristic extrarenal manifestations. While most ciliopathy-associated molecules are found in the cilium, Glis2/NPHP7 pre...

Descripción completa

Detalles Bibliográficos
Autores principales: Ramachandran, Haribaskar, Herfurth, Konstantin, Grosschedl, Rudolf, Schäfer, Tobias, Walz, Gerd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471195/
https://www.ncbi.nlm.nih.gov/pubmed/26083374
http://dx.doi.org/10.1371/journal.pone.0130275
_version_ 1782376865233633280
author Ramachandran, Haribaskar
Herfurth, Konstantin
Grosschedl, Rudolf
Schäfer, Tobias
Walz, Gerd
author_facet Ramachandran, Haribaskar
Herfurth, Konstantin
Grosschedl, Rudolf
Schäfer, Tobias
Walz, Gerd
author_sort Ramachandran, Haribaskar
collection PubMed
description Glis2/NPHP7 is a transcriptional regulator mutated in type 7 nephronophthisis, an autosomal recessive ciliopathy associated with cystic and fibrotic kidney disease as well as characteristic extrarenal manifestations. While most ciliopathy-associated molecules are found in the cilium, Glis2/NPHP7 presumably localizes to the nucleus. However, the detection of endogenous Glis2/NPHP7 has remained unsuccessful, potentially due to its ubiquitylation-dependent rapid degradation. We report now that Glis2/NPHP7 is also SUMOylated, preferentially by PIAS4, which conjugates Glis2/NPHP7 to SUMO3. SUMOylation interferes with ubiquitylation and degradation of Glis2/NPHP7, suggesting that Glis2/NPHP7 protein levels are regulated by competing ubiquitylation/ SUMOylation. SUMOylation also alters the transcriptional activity of Glis2/NPHP7. While Glis2/NPHP7 activates the mouse insulin-2-promotor (mIns2), SUMOylated Glis2/NPHP7 lacks this property, and seems to act as a repressor. Taken together, our data reveal that Glis2/NPHP7 is extensively modified by post-translational modifications, suggesting that a tight control of this transcriptional regulator is required for normal development and tissue homeostasis.
format Online
Article
Text
id pubmed-4471195
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-44711952015-06-29 SUMOylation Blocks the Ubiquitin-Mediated Degradation of the Nephronophthisis Gene Product Glis2/NPHP7 Ramachandran, Haribaskar Herfurth, Konstantin Grosschedl, Rudolf Schäfer, Tobias Walz, Gerd PLoS One Research Article Glis2/NPHP7 is a transcriptional regulator mutated in type 7 nephronophthisis, an autosomal recessive ciliopathy associated with cystic and fibrotic kidney disease as well as characteristic extrarenal manifestations. While most ciliopathy-associated molecules are found in the cilium, Glis2/NPHP7 presumably localizes to the nucleus. However, the detection of endogenous Glis2/NPHP7 has remained unsuccessful, potentially due to its ubiquitylation-dependent rapid degradation. We report now that Glis2/NPHP7 is also SUMOylated, preferentially by PIAS4, which conjugates Glis2/NPHP7 to SUMO3. SUMOylation interferes with ubiquitylation and degradation of Glis2/NPHP7, suggesting that Glis2/NPHP7 protein levels are regulated by competing ubiquitylation/ SUMOylation. SUMOylation also alters the transcriptional activity of Glis2/NPHP7. While Glis2/NPHP7 activates the mouse insulin-2-promotor (mIns2), SUMOylated Glis2/NPHP7 lacks this property, and seems to act as a repressor. Taken together, our data reveal that Glis2/NPHP7 is extensively modified by post-translational modifications, suggesting that a tight control of this transcriptional regulator is required for normal development and tissue homeostasis. Public Library of Science 2015-06-17 /pmc/articles/PMC4471195/ /pubmed/26083374 http://dx.doi.org/10.1371/journal.pone.0130275 Text en © 2015 Ramachandran 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.
spellingShingle Research Article
Ramachandran, Haribaskar
Herfurth, Konstantin
Grosschedl, Rudolf
Schäfer, Tobias
Walz, Gerd
SUMOylation Blocks the Ubiquitin-Mediated Degradation of the Nephronophthisis Gene Product Glis2/NPHP7
title SUMOylation Blocks the Ubiquitin-Mediated Degradation of the Nephronophthisis Gene Product Glis2/NPHP7
title_full SUMOylation Blocks the Ubiquitin-Mediated Degradation of the Nephronophthisis Gene Product Glis2/NPHP7
title_fullStr SUMOylation Blocks the Ubiquitin-Mediated Degradation of the Nephronophthisis Gene Product Glis2/NPHP7
title_full_unstemmed SUMOylation Blocks the Ubiquitin-Mediated Degradation of the Nephronophthisis Gene Product Glis2/NPHP7
title_short SUMOylation Blocks the Ubiquitin-Mediated Degradation of the Nephronophthisis Gene Product Glis2/NPHP7
title_sort sumoylation blocks the ubiquitin-mediated degradation of the nephronophthisis gene product glis2/nphp7
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471195/
https://www.ncbi.nlm.nih.gov/pubmed/26083374
http://dx.doi.org/10.1371/journal.pone.0130275
work_keys_str_mv AT ramachandranharibaskar sumoylationblockstheubiquitinmediateddegradationofthenephronophthisisgeneproductglis2nphp7
AT herfurthkonstantin sumoylationblockstheubiquitinmediateddegradationofthenephronophthisisgeneproductglis2nphp7
AT grosschedlrudolf sumoylationblockstheubiquitinmediateddegradationofthenephronophthisisgeneproductglis2nphp7
AT schafertobias sumoylationblockstheubiquitinmediateddegradationofthenephronophthisisgeneproductglis2nphp7
AT walzgerd sumoylationblockstheubiquitinmediateddegradationofthenephronophthisisgeneproductglis2nphp7