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SAF-A/hnRNP U binds polyphosphoinositides via a lysine rich polybasic motif located in the SAP domain

Polyphosphoinositides (PPIn) play essential functions as lipid signalling molecules and many of their functions have been elucidated in the cytoplasm. However, PPIn are also intranuclear where they contribute to chromatin remodelling, transcription and mRNA splicing. Using quantitative interactomics...

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Detalles Bibliográficos
Autores principales: Edson, Amanda J, Jacobsen, Rhîan G, Lewis, Aurélia E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Caltech Library 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082394/
https://www.ncbi.nlm.nih.gov/pubmed/37038481
http://dx.doi.org/10.17912/micropub.biology.000761
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author Edson, Amanda J
Jacobsen, Rhîan G
Lewis, Aurélia E
author_facet Edson, Amanda J
Jacobsen, Rhîan G
Lewis, Aurélia E
author_sort Edson, Amanda J
collection PubMed
description Polyphosphoinositides (PPIn) play essential functions as lipid signalling molecules and many of their functions have been elucidated in the cytoplasm. However, PPIn are also intranuclear where they contribute to chromatin remodelling, transcription and mRNA splicing. Using quantitative interactomics, we have previously identified PPIn-interacting proteins with roles in RNA processing/splicing including the heterogeneous nuclear ribonucleoprotein U (hnRNPU/SAF-A). In this study, hnRNPU was validated as a direct PPIn-interacting protein via 2 regions located in the N and C termini. Furthermore, deletion of the polybasic motif region located at aa 9-24 in its DNA binding SAP domain prevented PPIn interaction. In conclusion, these results are consistent with hnRNPU harbouring a polybasic region with dual functions in DNA and PPIn interaction.
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spelling pubmed-100823942023-04-09 SAF-A/hnRNP U binds polyphosphoinositides via a lysine rich polybasic motif located in the SAP domain Edson, Amanda J Jacobsen, Rhîan G Lewis, Aurélia E MicroPubl Biol New Finding Polyphosphoinositides (PPIn) play essential functions as lipid signalling molecules and many of their functions have been elucidated in the cytoplasm. However, PPIn are also intranuclear where they contribute to chromatin remodelling, transcription and mRNA splicing. Using quantitative interactomics, we have previously identified PPIn-interacting proteins with roles in RNA processing/splicing including the heterogeneous nuclear ribonucleoprotein U (hnRNPU/SAF-A). In this study, hnRNPU was validated as a direct PPIn-interacting protein via 2 regions located in the N and C termini. Furthermore, deletion of the polybasic motif region located at aa 9-24 in its DNA binding SAP domain prevented PPIn interaction. In conclusion, these results are consistent with hnRNPU harbouring a polybasic region with dual functions in DNA and PPIn interaction. Caltech Library 2023-03-24 /pmc/articles/PMC10082394/ /pubmed/37038481 http://dx.doi.org/10.17912/micropub.biology.000761 Text en Copyright: © 2023 by the authors https://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 credited.
spellingShingle New Finding
Edson, Amanda J
Jacobsen, Rhîan G
Lewis, Aurélia E
SAF-A/hnRNP U binds polyphosphoinositides via a lysine rich polybasic motif located in the SAP domain
title SAF-A/hnRNP U binds polyphosphoinositides via a lysine rich polybasic motif located in the SAP domain
title_full SAF-A/hnRNP U binds polyphosphoinositides via a lysine rich polybasic motif located in the SAP domain
title_fullStr SAF-A/hnRNP U binds polyphosphoinositides via a lysine rich polybasic motif located in the SAP domain
title_full_unstemmed SAF-A/hnRNP U binds polyphosphoinositides via a lysine rich polybasic motif located in the SAP domain
title_short SAF-A/hnRNP U binds polyphosphoinositides via a lysine rich polybasic motif located in the SAP domain
title_sort saf-a/hnrnp u binds polyphosphoinositides via a lysine rich polybasic motif located in the sap domain
topic New Finding
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082394/
https://www.ncbi.nlm.nih.gov/pubmed/37038481
http://dx.doi.org/10.17912/micropub.biology.000761
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