Cargando…

The Impact of p70S6 Kinase-Dependent Phosphorylation of Gemin2 in UsnRNP Biogenesis

The survival motor neuron (SMN) complex is a multi-megadalton complex involved in post-transcriptional gene expression in eukaryotes via promotion of the biogenesis of uridine-rich small nuclear ribonucleoproteins (UsnRNPs). The functional center of the complex is formed from the SMN/Gemin2 subunit....

Descripción completa

Detalles Bibliográficos
Autores principales: Esser, Lea Marie, Li, Qiaoping, Jüdt, Maximilian, Kähne, Thilo, Stork, Björn, Grimmler, Matthias, Wesselborg, Sebastian, Peter, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10649565/
https://www.ncbi.nlm.nih.gov/pubmed/37958537
http://dx.doi.org/10.3390/ijms242115552
_version_ 1785135581509976064
author Esser, Lea Marie
Li, Qiaoping
Jüdt, Maximilian
Kähne, Thilo
Stork, Björn
Grimmler, Matthias
Wesselborg, Sebastian
Peter, Christoph
author_facet Esser, Lea Marie
Li, Qiaoping
Jüdt, Maximilian
Kähne, Thilo
Stork, Björn
Grimmler, Matthias
Wesselborg, Sebastian
Peter, Christoph
author_sort Esser, Lea Marie
collection PubMed
description The survival motor neuron (SMN) complex is a multi-megadalton complex involved in post-transcriptional gene expression in eukaryotes via promotion of the biogenesis of uridine-rich small nuclear ribonucleoproteins (UsnRNPs). The functional center of the complex is formed from the SMN/Gemin2 subunit. By binding the pentameric ring made up of the Sm proteins SmD1/D2/E/F/G and allowing for their transfer to a uridine-rich short nuclear RNA (UsnRNA), the Gemin2 protein in particular is crucial for the selectivity of the Sm core assembly. It is well established that post-translational modifications control UsnRNP biogenesis. In our work presented here, we emphasize the crucial role of Gemin2, showing that the phospho-status of Gemin2 influences the capacity of the SMN complex to condense in Cajal bodies (CBs) in vivo. Additionally, we define Gemin2 as a novel and particular binding partner and phosphorylation substrate of the mTOR pathway kinase ribosomal protein S6 kinase beta-1 (p70S6K). Experiments using size exclusion chromatography further demonstrated that the Gemin2 protein functions as a connecting element between the 6S complex and the SMN complex. As a result, p70S6K knockdown lowered the number of CBs, which in turn inhibited in vivo UsnRNP synthesis. In summary, these findings reveal a unique regulatory mechanism of UsnRNP biogenesis.
format Online
Article
Text
id pubmed-10649565
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-106495652023-10-25 The Impact of p70S6 Kinase-Dependent Phosphorylation of Gemin2 in UsnRNP Biogenesis Esser, Lea Marie Li, Qiaoping Jüdt, Maximilian Kähne, Thilo Stork, Björn Grimmler, Matthias Wesselborg, Sebastian Peter, Christoph Int J Mol Sci Article The survival motor neuron (SMN) complex is a multi-megadalton complex involved in post-transcriptional gene expression in eukaryotes via promotion of the biogenesis of uridine-rich small nuclear ribonucleoproteins (UsnRNPs). The functional center of the complex is formed from the SMN/Gemin2 subunit. By binding the pentameric ring made up of the Sm proteins SmD1/D2/E/F/G and allowing for their transfer to a uridine-rich short nuclear RNA (UsnRNA), the Gemin2 protein in particular is crucial for the selectivity of the Sm core assembly. It is well established that post-translational modifications control UsnRNP biogenesis. In our work presented here, we emphasize the crucial role of Gemin2, showing that the phospho-status of Gemin2 influences the capacity of the SMN complex to condense in Cajal bodies (CBs) in vivo. Additionally, we define Gemin2 as a novel and particular binding partner and phosphorylation substrate of the mTOR pathway kinase ribosomal protein S6 kinase beta-1 (p70S6K). Experiments using size exclusion chromatography further demonstrated that the Gemin2 protein functions as a connecting element between the 6S complex and the SMN complex. As a result, p70S6K knockdown lowered the number of CBs, which in turn inhibited in vivo UsnRNP synthesis. In summary, these findings reveal a unique regulatory mechanism of UsnRNP biogenesis. MDPI 2023-10-25 /pmc/articles/PMC10649565/ /pubmed/37958537 http://dx.doi.org/10.3390/ijms242115552 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Esser, Lea Marie
Li, Qiaoping
Jüdt, Maximilian
Kähne, Thilo
Stork, Björn
Grimmler, Matthias
Wesselborg, Sebastian
Peter, Christoph
The Impact of p70S6 Kinase-Dependent Phosphorylation of Gemin2 in UsnRNP Biogenesis
title The Impact of p70S6 Kinase-Dependent Phosphorylation of Gemin2 in UsnRNP Biogenesis
title_full The Impact of p70S6 Kinase-Dependent Phosphorylation of Gemin2 in UsnRNP Biogenesis
title_fullStr The Impact of p70S6 Kinase-Dependent Phosphorylation of Gemin2 in UsnRNP Biogenesis
title_full_unstemmed The Impact of p70S6 Kinase-Dependent Phosphorylation of Gemin2 in UsnRNP Biogenesis
title_short The Impact of p70S6 Kinase-Dependent Phosphorylation of Gemin2 in UsnRNP Biogenesis
title_sort impact of p70s6 kinase-dependent phosphorylation of gemin2 in usnrnp biogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10649565/
https://www.ncbi.nlm.nih.gov/pubmed/37958537
http://dx.doi.org/10.3390/ijms242115552
work_keys_str_mv AT esserleamarie theimpactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis
AT liqiaoping theimpactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis
AT judtmaximilian theimpactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis
AT kahnethilo theimpactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis
AT storkbjorn theimpactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis
AT grimmlermatthias theimpactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis
AT wesselborgsebastian theimpactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis
AT peterchristoph theimpactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis
AT esserleamarie impactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis
AT liqiaoping impactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis
AT judtmaximilian impactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis
AT kahnethilo impactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis
AT storkbjorn impactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis
AT grimmlermatthias impactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis
AT wesselborgsebastian impactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis
AT peterchristoph impactofp70s6kinasedependentphosphorylationofgemin2inusnrnpbiogenesis